Pavićević, Ivan D.

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  • Pavićević, Ivan D. (10)
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Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu

Pavićević, Ivan D.

(Универзитет у Београду, Хемијски факултет, 2017)

TY  - THES
AU  - Pavićević, Ivan D.
PY  - 2017
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=5586
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:17084/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=49839375
UR  - http://nardus.mpn.gov.rs/123456789/9171
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2742
AB  - Humani serum albumin (HSA) je najzastupljeniji protein plazme sa udelomod oko 50 do 60 % svih proteina plazme. Vezuje i transportuje mnoge endogene iegzogene molekule, i doprinosi antioksidativnom kapacitetu seruma jer na površinimolekula poseduje jednu slobodnu tiolnu grupu ostatka Cys34. Slobodne masne kiseline(MK), koje transportuje HSA, i karbonilni stres mogli bi, kroz promenu reaktivnostitiolne grupe, uticati na njen potencijal kao hvatača reaktivnih karbonilnih vrsta. Stogasu ciljevi ove teze bili: in vitro ispitivanje uticaja 1) vezivanja MK, različite dužinelanca i zasićenosti na (i) reaktivnost Cys34-SH grupe, (ii) njen potencijal kao hvatačareaktivnih α-oksoaldehida, tj. na stepen karbonilacije i (iii) reaktivnost tiolne grupeHSA karbonilovanog metilglioksalom (model-sistem za molekule HSA modifikovane ukarbonilnom stresu); 2) vezivanja MK ribljeg ulja na reaktivnost Cys34-SH grupe(sagledavanje mogućnosti modulacije svojstava HSA pomoću suplemenata); 3)određivanje sadržaja Cys34-SH grupe, korelacija sa sadržajem HbA1c i glukoze ukarbonilnim stresom; 4) određivanje reaktivnosti Cys34-SH grupe HSA izolovanog izseruma dijabetičara i zdravih osoba; 5) razvijanje qTLC metode za određivanje sadržajaMK, vezanih za HSA, koji je izolovan iz realnih uzoraka.Vezivanje MK (različite dužine lanca i zasićenosti: miristinske (MYR),palmitinske (PLM), stearinske (STE), oleinske (OLA), eikozapentenske (EPA) idokozaheksaenske kiseline (DHA)) za HSA in vitro, dovodi do povećanja vrednostikonstanti brzine reakcije (k) Cys34 tiolne grupe (i DTNB) (k vrednosti kompleksa HSAMK:od 14,58±0,19 x 10-3 do 26,02±1,06 x 10-3 s-1 u odnosu na k HSA: 7,52±0,04 x 10-3 s-1), odnosno njene reaktivnosti za 2 do 3,5 puta. STE i OLA ispoljavaju slične efektena reaktivnost HSA-SH, a najjači efekat ispoljava polinezasićena EPA. Od zasićenihMK, najveća vrednost k dobijena je pri vezivanju MYR za HSA, što može biti posledicaizuzetne komplementarnosti njenog molekula sa vezivnim mestima na molekulu HSA,koja najviše utiču na izloženost tiolne grupe rastvaraču. Između vrednosti konstantibrzine reakcije Cys34-SH, dobijenih pri vezivanju različitih MK, i izračunatih vrednostidostupnosti Cys34 tiolne grupe rastvaraču nađen je visok stepen korelacije (r=0,927)...
AB  - Human serum albumin (HSA) is the most abundant protein of humanplasma, accounting for 50-60% of total plasma proteins. HSA binds and transport manyendogenous and exogenous substances, and contributes to the antioxidative pool inserum because of Cys34 free thiol group on the surface of its molecule. Free fatty acids(FAs), transported by HSA, and carbonyl stress could influence, through changedreactivity of the thiol group, on its potential as the scavenger of the reactive carbonylspecies. Therefore, the aims of this thesis were: in vitro examination of the influence 1)of different (in terms of chain length and saturation) FAs binding on the: (i) reactivity ofthe Cys34-SH group, (ii) its potential as the scavenger of the reactive α-oxoladehydes,and (iii) on the reactivity of the thiol group of HSA carbonylated with methylglyoxal(the model-system for HSA molecules modified during carbonyl stress); 2) of FAsfrom fish oil on the Cys34-SH group reactivity (overviewing the possibility of themodulation of the HSA scavenger properties with supplements); 3) determination of theCys34-SH group content, correlation with the HbA1c and glucose level of persons withelevated carbonyl stress; 4) determination of the Cys34-SH group reactivity of the HSAisolated from the sera of diabetic patients and healthy persons; 5) development of qTLCmethod for determination of the FAs content, bound to the HSA, which was isolatedfrom sera samples.Binding of FAs of different chain lengths and saturation (myristic (MYR),palmitic (PLM), stearic (STE), oleic (OLA), eicosapentaenoic (EPE) anddocosahexaenoic acid (DHA)) to the HSA in vitro resulting in increasing of the kineticsconstant (k) of the Cys34 thiol group reaction (with DTNB)(k values for HSA-FAscomplexes: from 14.58±0.19 ×10-3 to 26.02±1.06 × 10-3 s-1 comparing to k of the HSAsolely 7.52 ± 0.04 × 10-3 s-1), i.e. its reactivity for 2 to 3.5 times. STE and OLA showsimilar effects to the HSA-SH reactivity, and the strongest effect shows polyunsaturatedEPA. From saturated FAs binding to the HSA, the strongest effect shows MYR, andthat could be explained with extremely good fitting of the MYR molecule to the HSAFAs binding pockets which has the most influences to the exposure/accessibility of thethiol group to solvent...
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu
UR  - https://hdl.handle.net/21.15107/rcub_nardus_9171
ER  - 
@phdthesis{
author = "Pavićević, Ivan D.",
year = "2017",
abstract = "Humani serum albumin (HSA) je najzastupljeniji protein plazme sa udelomod oko 50 do 60 % svih proteina plazme. Vezuje i transportuje mnoge endogene iegzogene molekule, i doprinosi antioksidativnom kapacitetu seruma jer na površinimolekula poseduje jednu slobodnu tiolnu grupu ostatka Cys34. Slobodne masne kiseline(MK), koje transportuje HSA, i karbonilni stres mogli bi, kroz promenu reaktivnostitiolne grupe, uticati na njen potencijal kao hvatača reaktivnih karbonilnih vrsta. Stogasu ciljevi ove teze bili: in vitro ispitivanje uticaja 1) vezivanja MK, različite dužinelanca i zasićenosti na (i) reaktivnost Cys34-SH grupe, (ii) njen potencijal kao hvatačareaktivnih α-oksoaldehida, tj. na stepen karbonilacije i (iii) reaktivnost tiolne grupeHSA karbonilovanog metilglioksalom (model-sistem za molekule HSA modifikovane ukarbonilnom stresu); 2) vezivanja MK ribljeg ulja na reaktivnost Cys34-SH grupe(sagledavanje mogućnosti modulacije svojstava HSA pomoću suplemenata); 3)određivanje sadržaja Cys34-SH grupe, korelacija sa sadržajem HbA1c i glukoze ukarbonilnim stresom; 4) određivanje reaktivnosti Cys34-SH grupe HSA izolovanog izseruma dijabetičara i zdravih osoba; 5) razvijanje qTLC metode za određivanje sadržajaMK, vezanih za HSA, koji je izolovan iz realnih uzoraka.Vezivanje MK (različite dužine lanca i zasićenosti: miristinske (MYR),palmitinske (PLM), stearinske (STE), oleinske (OLA), eikozapentenske (EPA) idokozaheksaenske kiseline (DHA)) za HSA in vitro, dovodi do povećanja vrednostikonstanti brzine reakcije (k) Cys34 tiolne grupe (i DTNB) (k vrednosti kompleksa HSAMK:od 14,58±0,19 x 10-3 do 26,02±1,06 x 10-3 s-1 u odnosu na k HSA: 7,52±0,04 x 10-3 s-1), odnosno njene reaktivnosti za 2 do 3,5 puta. STE i OLA ispoljavaju slične efektena reaktivnost HSA-SH, a najjači efekat ispoljava polinezasićena EPA. Od zasićenihMK, najveća vrednost k dobijena je pri vezivanju MYR za HSA, što može biti posledicaizuzetne komplementarnosti njenog molekula sa vezivnim mestima na molekulu HSA,koja najviše utiču na izloženost tiolne grupe rastvaraču. Između vrednosti konstantibrzine reakcije Cys34-SH, dobijenih pri vezivanju različitih MK, i izračunatih vrednostidostupnosti Cys34 tiolne grupe rastvaraču nađen je visok stepen korelacije (r=0,927)..., Human serum albumin (HSA) is the most abundant protein of humanplasma, accounting for 50-60% of total plasma proteins. HSA binds and transport manyendogenous and exogenous substances, and contributes to the antioxidative pool inserum because of Cys34 free thiol group on the surface of its molecule. Free fatty acids(FAs), transported by HSA, and carbonyl stress could influence, through changedreactivity of the thiol group, on its potential as the scavenger of the reactive carbonylspecies. Therefore, the aims of this thesis were: in vitro examination of the influence 1)of different (in terms of chain length and saturation) FAs binding on the: (i) reactivity ofthe Cys34-SH group, (ii) its potential as the scavenger of the reactive α-oxoladehydes,and (iii) on the reactivity of the thiol group of HSA carbonylated with methylglyoxal(the model-system for HSA molecules modified during carbonyl stress); 2) of FAsfrom fish oil on the Cys34-SH group reactivity (overviewing the possibility of themodulation of the HSA scavenger properties with supplements); 3) determination of theCys34-SH group content, correlation with the HbA1c and glucose level of persons withelevated carbonyl stress; 4) determination of the Cys34-SH group reactivity of the HSAisolated from the sera of diabetic patients and healthy persons; 5) development of qTLCmethod for determination of the FAs content, bound to the HSA, which was isolatedfrom sera samples.Binding of FAs of different chain lengths and saturation (myristic (MYR),palmitic (PLM), stearic (STE), oleic (OLA), eicosapentaenoic (EPE) anddocosahexaenoic acid (DHA)) to the HSA in vitro resulting in increasing of the kineticsconstant (k) of the Cys34 thiol group reaction (with DTNB)(k values for HSA-FAscomplexes: from 14.58±0.19 ×10-3 to 26.02±1.06 × 10-3 s-1 comparing to k of the HSAsolely 7.52 ± 0.04 × 10-3 s-1), i.e. its reactivity for 2 to 3.5 times. STE and OLA showsimilar effects to the HSA-SH reactivity, and the strongest effect shows polyunsaturatedEPA. From saturated FAs binding to the HSA, the strongest effect shows MYR, andthat could be explained with extremely good fitting of the MYR molecule to the HSAFAs binding pockets which has the most influences to the exposure/accessibility of thethiol group to solvent...",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu",
url = "https://hdl.handle.net/21.15107/rcub_nardus_9171"
}
Pavićević, I. D.. (2017). Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_9171
Pavićević ID. Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu. in Универзитет у Београду. 2017;.
https://hdl.handle.net/21.15107/rcub_nardus_9171 .
Pavićević, Ivan D., "Promene reaktivnosti tiolne grupe Cys34 humanog serum-albumina pri vezivanju masnih kiselina in vitro i u karbonilnom stresu" in Универзитет у Београду (2017),
https://hdl.handle.net/21.15107/rcub_nardus_9171 .

Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity

Takić, Marija M.; Jovanović, Vesna B.; Pavićević, Ivan D.; Uzelac, Tamara N.; Aćimović, Jelena M.; Ristić-Medić, Danijela; Mandić, Ljuba M.

(Royal Soc Chemistry, Cambridge, 2016)

TY  - JOUR
AU  - Takić, Marija M.
AU  - Jovanović, Vesna B.
AU  - Pavićević, Ivan D.
AU  - Uzelac, Tamara N.
AU  - Aćimović, Jelena M.
AU  - Ristić-Medić, Danijela
AU  - Mandić, Ljuba M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2054
AB  - The interaction of polyphenolic molecules with human serum albumin (HSA) could lead to changes in the reactivity of the HSA Cys34 thiol group (HSA-SH). The influences of enterolactone (EL) and enterodiol (ED) binding on HSA-SH reactivity in fatty acid (FA)-free HSA, and in HSA with bound stearic acid (S) in S/HSA molar ratios of 1 : 1 and 4 : 1, were investigated by the determination of the pseudo first order rate constants (k') for the thiol reaction with 5,5'-dithiobis-(2-nitrobenzoic acid). The binding affinities and binding sites of EL and ED were also determined, using fluorescence measurements of the intrinsic fluorescence of Trp214 and diazepam (binding site marker). EL and ED binding to HSA increased the reactivity of HSA-SH in all assayed HSA-enterolignan complexes by 9.1-33.1%. The strongest effects were obtained for FA-free HSA-enterolignan complexes. S modulated/reduced the effect of EL on HSA-SH reactivity, while its influence on the effect of ED was negligible. The binding of enterolignans to HSA was investigated: the binding constants were the highest for FA-free HSA (EL: 11.64 x 10(4) M-1 and ED: 5.59 x 10(4) M-1 at 37 degrees C) and the lowest for S/HSA 4 : 1-enterolignan complexes (EL: 2.43 x 10(4) M-1 and ED: 1.92 x 10(4) M-1). When the S/HSA ratio was increased, the binding affinities and number of binding sites for EL and ED were decreased. At the same time, a high correlation between binding constants and increased Cys34 reactivity was found (r = 0.974). Competitive experiments using diazepam indicated that the binding of ED and of EL was located in the hydrophobic pocket of site II in HSA. Overall, it is evident that stearic acid could modulate the enterolignan effects on HSA-SH reactivity as well as their binding to HSA. This finding could be important for pharmacokinetics and the expression of enterolignan antioxidant effects in vivo after an intake of lignan rich food.
PB  - Royal Soc Chemistry, Cambridge
T2  - Food and Function
T1  - Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity
VL  - 7
IS  - 2
SP  - 1217
EP  - 1226
DO  - 10.1039/c5fo01346a
ER  - 
@article{
author = "Takić, Marija M. and Jovanović, Vesna B. and Pavićević, Ivan D. and Uzelac, Tamara N. and Aćimović, Jelena M. and Ristić-Medić, Danijela and Mandić, Ljuba M.",
year = "2016",
abstract = "The interaction of polyphenolic molecules with human serum albumin (HSA) could lead to changes in the reactivity of the HSA Cys34 thiol group (HSA-SH). The influences of enterolactone (EL) and enterodiol (ED) binding on HSA-SH reactivity in fatty acid (FA)-free HSA, and in HSA with bound stearic acid (S) in S/HSA molar ratios of 1 : 1 and 4 : 1, were investigated by the determination of the pseudo first order rate constants (k') for the thiol reaction with 5,5'-dithiobis-(2-nitrobenzoic acid). The binding affinities and binding sites of EL and ED were also determined, using fluorescence measurements of the intrinsic fluorescence of Trp214 and diazepam (binding site marker). EL and ED binding to HSA increased the reactivity of HSA-SH in all assayed HSA-enterolignan complexes by 9.1-33.1%. The strongest effects were obtained for FA-free HSA-enterolignan complexes. S modulated/reduced the effect of EL on HSA-SH reactivity, while its influence on the effect of ED was negligible. The binding of enterolignans to HSA was investigated: the binding constants were the highest for FA-free HSA (EL: 11.64 x 10(4) M-1 and ED: 5.59 x 10(4) M-1 at 37 degrees C) and the lowest for S/HSA 4 : 1-enterolignan complexes (EL: 2.43 x 10(4) M-1 and ED: 1.92 x 10(4) M-1). When the S/HSA ratio was increased, the binding affinities and number of binding sites for EL and ED were decreased. At the same time, a high correlation between binding constants and increased Cys34 reactivity was found (r = 0.974). Competitive experiments using diazepam indicated that the binding of ED and of EL was located in the hydrophobic pocket of site II in HSA. Overall, it is evident that stearic acid could modulate the enterolignan effects on HSA-SH reactivity as well as their binding to HSA. This finding could be important for pharmacokinetics and the expression of enterolignan antioxidant effects in vivo after an intake of lignan rich food.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Food and Function",
title = "Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity",
volume = "7",
number = "2",
pages = "1217-1226",
doi = "10.1039/c5fo01346a"
}
Takić, M. M., Jovanović, V. B., Pavićević, I. D., Uzelac, T. N., Aćimović, J. M., Ristić-Medić, D.,& Mandić, L. M.. (2016). Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity. in Food and Function
Royal Soc Chemistry, Cambridge., 7(2), 1217-1226.
https://doi.org/10.1039/c5fo01346a
Takić MM, Jovanović VB, Pavićević ID, Uzelac TN, Aćimović JM, Ristić-Medić D, Mandić LM. Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity. in Food and Function. 2016;7(2):1217-1226.
doi:10.1039/c5fo01346a .
Takić, Marija M., Jovanović, Vesna B., Pavićević, Ivan D., Uzelac, Tamara N., Aćimović, Jelena M., Ristić-Medić, Danijela, Mandić, Ljuba M., "Binding of enterolactone and enterodiol to human serum albumin: increase of cysteine-34 thiol group reactivity" in Food and Function, 7, no. 2 (2016):1217-1226,
https://doi.org/10.1039/c5fo01346a . .
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Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal

Aćimović, Jelena M.; Penezić, Ana Z.; Pavićević, Ivan D.; Jovanović, Vesna B.; Takić, Marija M.; Uzelac, T. N.; Mandić, Ljuba M.

(Wiley-Blackwell, Hoboken, 2016)

TY  - CONF
AU  - Aćimović, Jelena M.
AU  - Penezić, Ana Z.
AU  - Pavićević, Ivan D.
AU  - Jovanović, Vesna B.
AU  - Takić, Marija M.
AU  - Uzelac, T. N.
AU  - Mandić, Ljuba M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2307
PB  - Wiley-Blackwell, Hoboken
C3  - FEBS Journal / Federation of European of Biochemical Societies
T1  - Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal
VL  - 283
SP  - 417
EP  - 417
UR  - https://hdl.handle.net/21.15107/rcub_cherry_2307
ER  - 
@conference{
author = "Aćimović, Jelena M. and Penezić, Ana Z. and Pavićević, Ivan D. and Jovanović, Vesna B. and Takić, Marija M. and Uzelac, T. N. and Mandić, Ljuba M.",
year = "2016",
publisher = "Wiley-Blackwell, Hoboken",
journal = "FEBS Journal / Federation of European of Biochemical Societies",
title = "Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal",
volume = "283",
pages = "417-417",
url = "https://hdl.handle.net/21.15107/rcub_cherry_2307"
}
Aćimović, J. M., Penezić, A. Z., Pavićević, I. D., Jovanović, V. B., Takić, M. M., Uzelac, T. N.,& Mandić, L. M.. (2016). Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal. in FEBS Journal / Federation of European of Biochemical Societies
Wiley-Blackwell, Hoboken., 283, 417-417.
https://hdl.handle.net/21.15107/rcub_cherry_2307
Aćimović JM, Penezić AZ, Pavićević ID, Jovanović VB, Takić MM, Uzelac TN, Mandić LM. Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal. in FEBS Journal / Federation of European of Biochemical Societies. 2016;283:417-417.
https://hdl.handle.net/21.15107/rcub_cherry_2307 .
Aćimović, Jelena M., Penezić, Ana Z., Pavićević, Ivan D., Jovanović, Vesna B., Takić, Marija M., Uzelac, T. N., Mandić, Ljuba M., "Binding of FAs and Cu(II) ions to HSA changes its Cys34 thiol group antioxidant capacity and carbonylation pattern with methylglyoxal" in FEBS Journal / Federation of European of Biochemical Societies, 283 (2016):417-417,
https://hdl.handle.net/21.15107/rcub_cherry_2307 .

Quantification of total content of non-esterified fatty acids bound to human serum albumin

Pavićević, Ivan D.; Jovanović, Vesna B.; Takić, Marija M.; Aćimović, Jelena M.; Penezić, Ana Z.; Mandić, Ljuba M.

(Elsevier Science Bv, Amsterdam, 2016)

TY  - JOUR
AU  - Pavićević, Ivan D.
AU  - Jovanović, Vesna B.
AU  - Takić, Marija M.
AU  - Aćimović, Jelena M.
AU  - Penezić, Ana Z.
AU  - Mandić, Ljuba M.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2399
AB  - Non-esterified fatty acids bound to the human serum albumin (HSA) contribute to several HSAs properties of special concern in pathologies, for instance to the reactivity of the free HSA-Cys34 thiol group (important antioxidative thiol pool in plasma), and to the affinity for binding of molecules and ions (for example cobalt as a prominent biomarker in heart ischemia). Therefore, the method for determination of FAs bound to HSA was developed. FAs were released from HSA (previously isolated from serum by ammonium sulfate precipitation) using acidic copper(II) sulfate in phosphoric acid, extracted by n-heptane-chloroform (4:1, v/v) mixture, spotted on TL silica-gel and then developed with n-heptane-chloroform-acetic acid (5:3:03, v/v/v). Common office flatbed scanner and software solution for densitometric image analysis, developed in R, were used. The linearity of calibration curve in concentration range from 0.1 to 5.0 mmol/L stearic acid was achieved. The method was proved to be precise (with RSD of 1.4-4.7%) and accurate. Accuracy was examined by standard addition method (recoveries 97.2-102.5%) and by comparison to results of GC. The method is sample saving, technically less demanding, and cheap, and therefore suitable for determination of FAs/HSA ratio when elevated concentrations of free FAs are reliable diagnostic/risk parameter of pathological states. (C) 2016 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Quantification of total content of non-esterified fatty acids bound to human serum albumin
VL  - 129
SP  - 43
EP  - 49
DO  - 10.1016/j.jpba.2016.06.043
ER  - 
@article{
author = "Pavićević, Ivan D. and Jovanović, Vesna B. and Takić, Marija M. and Aćimović, Jelena M. and Penezić, Ana Z. and Mandić, Ljuba M.",
year = "2016",
abstract = "Non-esterified fatty acids bound to the human serum albumin (HSA) contribute to several HSAs properties of special concern in pathologies, for instance to the reactivity of the free HSA-Cys34 thiol group (important antioxidative thiol pool in plasma), and to the affinity for binding of molecules and ions (for example cobalt as a prominent biomarker in heart ischemia). Therefore, the method for determination of FAs bound to HSA was developed. FAs were released from HSA (previously isolated from serum by ammonium sulfate precipitation) using acidic copper(II) sulfate in phosphoric acid, extracted by n-heptane-chloroform (4:1, v/v) mixture, spotted on TL silica-gel and then developed with n-heptane-chloroform-acetic acid (5:3:03, v/v/v). Common office flatbed scanner and software solution for densitometric image analysis, developed in R, were used. The linearity of calibration curve in concentration range from 0.1 to 5.0 mmol/L stearic acid was achieved. The method was proved to be precise (with RSD of 1.4-4.7%) and accurate. Accuracy was examined by standard addition method (recoveries 97.2-102.5%) and by comparison to results of GC. The method is sample saving, technically less demanding, and cheap, and therefore suitable for determination of FAs/HSA ratio when elevated concentrations of free FAs are reliable diagnostic/risk parameter of pathological states. (C) 2016 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Quantification of total content of non-esterified fatty acids bound to human serum albumin",
volume = "129",
pages = "43-49",
doi = "10.1016/j.jpba.2016.06.043"
}
Pavićević, I. D., Jovanović, V. B., Takić, M. M., Aćimović, J. M., Penezić, A. Z.,& Mandić, L. M.. (2016). Quantification of total content of non-esterified fatty acids bound to human serum albumin. in Journal of Pharmaceutical and Biomedical Analysis
Elsevier Science Bv, Amsterdam., 129, 43-49.
https://doi.org/10.1016/j.jpba.2016.06.043
Pavićević ID, Jovanović VB, Takić MM, Aćimović JM, Penezić AZ, Mandić LM. Quantification of total content of non-esterified fatty acids bound to human serum albumin. in Journal of Pharmaceutical and Biomedical Analysis. 2016;129:43-49.
doi:10.1016/j.jpba.2016.06.043 .
Pavićević, Ivan D., Jovanović, Vesna B., Takić, Marija M., Aćimović, Jelena M., Penezić, Ana Z., Mandić, Ljuba M., "Quantification of total content of non-esterified fatty acids bound to human serum albumin" in Journal of Pharmaceutical and Biomedical Analysis, 129 (2016):43-49,
https://doi.org/10.1016/j.jpba.2016.06.043 . .
1
4
1
3
3

HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions

Penezić, Ana Z.; Jovanović, Vesna B.; Pavićević, Ivan D.; Aćimović, Jelena M.; Mandić, Ljuba M.

(Royal Soc Chemistry, Cambridge, 2015)

TY  - JOUR
AU  - Penezić, Ana Z.
AU  - Jovanović, Vesna B.
AU  - Pavićević, Ivan D.
AU  - Aćimović, Jelena M.
AU  - Mandić, Ljuba M.
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1979
AB  - The potential of carbonylation with methylglyoxal to alter HSA's binding affinity for copper(II) ions and its influence on the release of copper(II) ions from copper-HSA complexes were studied. The affinity of HSA to coordinate copper(II) decreased upon carbonylation of the Cys34-SH group. Carbonylation of copper-HSA complexes caused a decrease in Cys34-SH content, conformational changes and the release of copper(II) ions. The ratio between the percentage of reduction in the Cys34-SH group content and the percentage of release of copper(II) from complexes is 2.12 +/- 0.28. Because the same ratio (1.96 +/- 0.36) was obtained upon oxidation of the Cys34-SH group (with no changes in HSA conformation), the binding/release of copper (II) by HSA depended mainly on the redox state of the Cys34-SH group. The contents of Cys34-SH and HSA-bound copper(II) ions in the diabetic group (0.457 +/- 0.081 mol SH per mol HSA, 10.7 +/- 0.01 mmol per mol HSA, resp.) were significantly lower (p  lt  0.01) compared to the control group (0.609 +/- 0.027 mol SH per mol HSA; 13.4 +/- 0.01 mmol per mol HSA, resp.). Very strong correlations between the values for HSA-SH and glycated haemoglobin, HbA1c, (R = -0.803, p  lt  0.01), and between the values for the HSA-bound copper(II) content and HSA-SH content (R = 0.841, p  lt  0.002) were found in the diabetic group. Thus, HSA carbonylation leads to decrease in HSA-SH content and to the impairment of its copper(II) binding capacity that could contribute to further enhancement of oxidative and carbonyl stress in diabetes (as well as in other diseases with carbonyl stress).
PB  - Royal Soc Chemistry, Cambridge
T2  - Metallomics
T1  - HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions
VL  - 7
IS  - 10
SP  - 1431
EP  - 1438
DO  - 10.1039/c5mt00159e
ER  - 
@article{
author = "Penezić, Ana Z. and Jovanović, Vesna B. and Pavićević, Ivan D. and Aćimović, Jelena M. and Mandić, Ljuba M.",
year = "2015",
abstract = "The potential of carbonylation with methylglyoxal to alter HSA's binding affinity for copper(II) ions and its influence on the release of copper(II) ions from copper-HSA complexes were studied. The affinity of HSA to coordinate copper(II) decreased upon carbonylation of the Cys34-SH group. Carbonylation of copper-HSA complexes caused a decrease in Cys34-SH content, conformational changes and the release of copper(II) ions. The ratio between the percentage of reduction in the Cys34-SH group content and the percentage of release of copper(II) from complexes is 2.12 +/- 0.28. Because the same ratio (1.96 +/- 0.36) was obtained upon oxidation of the Cys34-SH group (with no changes in HSA conformation), the binding/release of copper (II) by HSA depended mainly on the redox state of the Cys34-SH group. The contents of Cys34-SH and HSA-bound copper(II) ions in the diabetic group (0.457 +/- 0.081 mol SH per mol HSA, 10.7 +/- 0.01 mmol per mol HSA, resp.) were significantly lower (p  lt  0.01) compared to the control group (0.609 +/- 0.027 mol SH per mol HSA; 13.4 +/- 0.01 mmol per mol HSA, resp.). Very strong correlations between the values for HSA-SH and glycated haemoglobin, HbA1c, (R = -0.803, p  lt  0.01), and between the values for the HSA-bound copper(II) content and HSA-SH content (R = 0.841, p  lt  0.002) were found in the diabetic group. Thus, HSA carbonylation leads to decrease in HSA-SH content and to the impairment of its copper(II) binding capacity that could contribute to further enhancement of oxidative and carbonyl stress in diabetes (as well as in other diseases with carbonyl stress).",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Metallomics",
title = "HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions",
volume = "7",
number = "10",
pages = "1431-1438",
doi = "10.1039/c5mt00159e"
}
Penezić, A. Z., Jovanović, V. B., Pavićević, I. D., Aćimović, J. M.,& Mandić, L. M.. (2015). HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions. in Metallomics
Royal Soc Chemistry, Cambridge., 7(10), 1431-1438.
https://doi.org/10.1039/c5mt00159e
Penezić AZ, Jovanović VB, Pavićević ID, Aćimović JM, Mandić LM. HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions. in Metallomics. 2015;7(10):1431-1438.
doi:10.1039/c5mt00159e .
Penezić, Ana Z., Jovanović, Vesna B., Pavićević, Ivan D., Aćimović, Jelena M., Mandić, Ljuba M., "HSA carbonylation with methylglyoxal and the binding/release of copper(II) ions" in Metallomics, 7, no. 10 (2015):1431-1438,
https://doi.org/10.1039/c5mt00159e . .
8
6
8
8

Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal

Pavićević, Ivan D.; Jovanović, Vesna B.; Takić, Marija M.; Penezić, Ana Z.; Aćimović, Jelena M.; Mandić, Ljuba M.

(Elsevier Ireland Ltd, Clare, 2014)

TY  - JOUR
AU  - Pavićević, Ivan D.
AU  - Jovanović, Vesna B.
AU  - Takić, Marija M.
AU  - Penezić, Ana Z.
AU  - Aćimović, Jelena M.
AU  - Mandić, Ljuba M.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1895
AB  - Fatty acids (FAs) binding to human serum albumin (HSA) could lead to the changes of Cys-34 thiol group accessibility and reactivity, i.e. its scavenger capacity and antioxidant property. The influence of saturated, mono and poly unsaturated, and fish oil FAs binding to HSA on the carbonylation level and the reactivity of HSA-SH and HSA modified with methylglyoxal (MG-HSA-SH) was investigated. Changes of thiol group reactivity were followed by determination of pseudo first order rate constant (k') for thiols reaction with 5,5'-dithiobis(2-nitrobenzoic acid). HSA changes were monitored using native PAG electrophoresis and fluorescence spectroscopy. For FA/HSA molar ratios screening, qTLC and GC were used. FAs increase thiol group carbonylation levels from 8% to 20%. The k' values obtained for FAs-free HSA-SH and FAs-free MG-HSA-SH are almost equal (7.5 x 10(-3) and 7.7 x 10(-3) resp.). Binding of all FAs amplify the reactivity (k' values from 14.6 x 10(-3) to 26.0 x 10(-3) s(-1)) of HSA-SH group for 2-3.5 times in the order: palmitic, docosahexaenoic, fish oil extract, stearic, oleic, myristic and eicosapentaenoic acid, due to HSA conformational changes. FAs-bound MG-HSA-SH samples follow that pattern, but their k' values (from 9.8 x 10(-3) to 14.3 x 10(-3) s(-1)) were lower compared to unmodified HSA due to additional conformation changes of HSA molecules during carbonylation. Carbonylation level and reactivity of Cys34 thiol group of unmodified and carbonylated HSA depend on type of FAs bound to HSA, which implies the possibility for modulation of -SH reactivity (scavenger capacity and antioxidant property) by FAs as a supplement. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
PB  - Elsevier Ireland Ltd, Clare
T2  - Chemico-biological Interactions
T1  - Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal
VL  - 224
SP  - 42
EP  - 50
DO  - 10.1016/j.cbi.2014.10.008
ER  - 
@article{
author = "Pavićević, Ivan D. and Jovanović, Vesna B. and Takić, Marija M. and Penezić, Ana Z. and Aćimović, Jelena M. and Mandić, Ljuba M.",
year = "2014",
abstract = "Fatty acids (FAs) binding to human serum albumin (HSA) could lead to the changes of Cys-34 thiol group accessibility and reactivity, i.e. its scavenger capacity and antioxidant property. The influence of saturated, mono and poly unsaturated, and fish oil FAs binding to HSA on the carbonylation level and the reactivity of HSA-SH and HSA modified with methylglyoxal (MG-HSA-SH) was investigated. Changes of thiol group reactivity were followed by determination of pseudo first order rate constant (k') for thiols reaction with 5,5'-dithiobis(2-nitrobenzoic acid). HSA changes were monitored using native PAG electrophoresis and fluorescence spectroscopy. For FA/HSA molar ratios screening, qTLC and GC were used. FAs increase thiol group carbonylation levels from 8% to 20%. The k' values obtained for FAs-free HSA-SH and FAs-free MG-HSA-SH are almost equal (7.5 x 10(-3) and 7.7 x 10(-3) resp.). Binding of all FAs amplify the reactivity (k' values from 14.6 x 10(-3) to 26.0 x 10(-3) s(-1)) of HSA-SH group for 2-3.5 times in the order: palmitic, docosahexaenoic, fish oil extract, stearic, oleic, myristic and eicosapentaenoic acid, due to HSA conformational changes. FAs-bound MG-HSA-SH samples follow that pattern, but their k' values (from 9.8 x 10(-3) to 14.3 x 10(-3) s(-1)) were lower compared to unmodified HSA due to additional conformation changes of HSA molecules during carbonylation. Carbonylation level and reactivity of Cys34 thiol group of unmodified and carbonylated HSA depend on type of FAs bound to HSA, which implies the possibility for modulation of -SH reactivity (scavenger capacity and antioxidant property) by FAs as a supplement. (C) 2014 Elsevier Ireland Ltd. All rights reserved.",
publisher = "Elsevier Ireland Ltd, Clare",
journal = "Chemico-biological Interactions",
title = "Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal",
volume = "224",
pages = "42-50",
doi = "10.1016/j.cbi.2014.10.008"
}
Pavićević, I. D., Jovanović, V. B., Takić, M. M., Penezić, A. Z., Aćimović, J. M.,& Mandić, L. M.. (2014). Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal. in Chemico-biological Interactions
Elsevier Ireland Ltd, Clare., 224, 42-50.
https://doi.org/10.1016/j.cbi.2014.10.008
Pavićević ID, Jovanović VB, Takić MM, Penezić AZ, Aćimović JM, Mandić LM. Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal. in Chemico-biological Interactions. 2014;224:42-50.
doi:10.1016/j.cbi.2014.10.008 .
Pavićević, Ivan D., Jovanović, Vesna B., Takić, Marija M., Penezić, Ana Z., Aćimović, Jelena M., Mandić, Ljuba M., "Fatty acids binding to human serum albumin: Changes of reactivity and glycation level of Cysteine-34 free thiol group with methylglyoxal" in Chemico-biological Interactions, 224 (2014):42-50,
https://doi.org/10.1016/j.cbi.2014.10.008 . .
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26

The influence of fatty acids on determination of human serum albumin thiol group

Jovanović, Vesna B.; Pavićević, Ivan D.; Takić, Marija M.; Penezić-Romanjuk, Ana Z.; Aćimović, Jelena M.; Mandić, Ljuba M.

(Academic Press Inc Elsevier Science, San Diego, 2014)

TY  - JOUR
AU  - Jovanović, Vesna B.
AU  - Pavićević, Ivan D.
AU  - Takić, Marija M.
AU  - Penezić-Romanjuk, Ana Z.
AU  - Aćimović, Jelena M.
AU  - Mandić, Ljuba M.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1476
AB  - During investigation of the changes of the Cys34 thiol group of human serum albumin (HSA) (isolated by affinity chromatography with Cibacron Blue (CB)) in diabetes, we found that the HSA-SH content was higher (11-33%) than the total serum thiol content. The influence of fatty acids (FA) binding to HSA on this discrepancy was investigated in vitro (using fluorescence and CD spectroscopy and GC) and with HSA samples from diabetic (n=20) and control groups (n=17). HSA-bound FA determine the selection of HSA molecules by CB and enhance reactivity and/or accessibility of the SH group. A high content of polyunsaturated FA (35.6%) leads to weaker binding of HSA molecules to CB. Rate constants of DTNB reaction with the SH group of HSA applied to a CB column, bound-HSA and unbound-HSA fractions, were 4.8 x 10(-3), 21.6 x 10(-3), and 11.2 x 10(-3) s(-1), respectively. The HSA-SH group of diabetics is more reactive compared with control individuals (rate constants 20.9 x 10(-3)+/- 4.4 x 10(-3) vs 12.9 x 10(-3)+/- 2.6 x 10(-3) s(-1), P lt 0.05). Recovery values of the SH group obtained after chromatography of HSA with bound stearic acid ranged from 110 to 140%, while those for defatted HSA were from 98.5 to 101.7%. Thus, HSA-bound FA leads to an increase of HSA-SH content and a contribution to total serum thiols, which make the determination of the thiol group unreliable. (C) 2013 Elsevier Inc. All rights reserved.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Analytical Biochemistry
T1  - The influence of fatty acids on determination of human serum albumin thiol group
VL  - 448
SP  - 50
EP  - 57
DO  - 10.1016/j.ab.2013.11.030
ER  - 
@article{
author = "Jovanović, Vesna B. and Pavićević, Ivan D. and Takić, Marija M. and Penezić-Romanjuk, Ana Z. and Aćimović, Jelena M. and Mandić, Ljuba M.",
year = "2014",
abstract = "During investigation of the changes of the Cys34 thiol group of human serum albumin (HSA) (isolated by affinity chromatography with Cibacron Blue (CB)) in diabetes, we found that the HSA-SH content was higher (11-33%) than the total serum thiol content. The influence of fatty acids (FA) binding to HSA on this discrepancy was investigated in vitro (using fluorescence and CD spectroscopy and GC) and with HSA samples from diabetic (n=20) and control groups (n=17). HSA-bound FA determine the selection of HSA molecules by CB and enhance reactivity and/or accessibility of the SH group. A high content of polyunsaturated FA (35.6%) leads to weaker binding of HSA molecules to CB. Rate constants of DTNB reaction with the SH group of HSA applied to a CB column, bound-HSA and unbound-HSA fractions, were 4.8 x 10(-3), 21.6 x 10(-3), and 11.2 x 10(-3) s(-1), respectively. The HSA-SH group of diabetics is more reactive compared with control individuals (rate constants 20.9 x 10(-3)+/- 4.4 x 10(-3) vs 12.9 x 10(-3)+/- 2.6 x 10(-3) s(-1), P lt 0.05). Recovery values of the SH group obtained after chromatography of HSA with bound stearic acid ranged from 110 to 140%, while those for defatted HSA were from 98.5 to 101.7%. Thus, HSA-bound FA leads to an increase of HSA-SH content and a contribution to total serum thiols, which make the determination of the thiol group unreliable. (C) 2013 Elsevier Inc. All rights reserved.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Analytical Biochemistry",
title = "The influence of fatty acids on determination of human serum albumin thiol group",
volume = "448",
pages = "50-57",
doi = "10.1016/j.ab.2013.11.030"
}
Jovanović, V. B., Pavićević, I. D., Takić, M. M., Penezić-Romanjuk, A. Z., Aćimović, J. M.,& Mandić, L. M.. (2014). The influence of fatty acids on determination of human serum albumin thiol group. in Analytical Biochemistry
Academic Press Inc Elsevier Science, San Diego., 448, 50-57.
https://doi.org/10.1016/j.ab.2013.11.030
Jovanović VB, Pavićević ID, Takić MM, Penezić-Romanjuk AZ, Aćimović JM, Mandić LM. The influence of fatty acids on determination of human serum albumin thiol group. in Analytical Biochemistry. 2014;448:50-57.
doi:10.1016/j.ab.2013.11.030 .
Jovanović, Vesna B., Pavićević, Ivan D., Takić, Marija M., Penezić-Romanjuk, Ana Z., Aćimović, Jelena M., Mandić, Ljuba M., "The influence of fatty acids on determination of human serum albumin thiol group" in Analytical Biochemistry, 448 (2014):50-57,
https://doi.org/10.1016/j.ab.2013.11.030 . .
16
11
16
14

The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal

Aćimović, Jelena M.; Penezić, Ana Z.; Pavićević, Ivan D.; Jovanović, Vesna B.; Mandić, Ljuba M.

(Royal Soc Chemistry, Cambridge, 2014)

TY  - JOUR
AU  - Aćimović, Jelena M.
AU  - Penezić, Ana Z.
AU  - Pavićević, Ivan D.
AU  - Jovanović, Vesna B.
AU  - Mandić, Ljuba M.
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1814
AB  - alpha-Oxoaldehydes, which are produced in higher quantities in diabetes, uremia, oxidative stress, inflammation and aging, react with the amino, guanidine and thiol groups of proteins and cause the formation of advanced glycated end-products and protein cross-linking. To prevent these reactions, the efficiency of tow molecular mass thiols with an alpha-amino-beta-mercapto-ethane group (Cys, penicillamine and N-acetylcysteine (NAcCys, with a blocked amino group)) as scavengers of methylglyoxal, compared with glutathione (GSH) and the biguanidine derivative metformin, was investigated. The time courses of the reactions of the aforementioned compounds with methylglyoxal were assayed. The reactivity of their thiol and amino groups decreased in the order of Cys  gt  penicillamine  gt  GSH  gt  NAcCys and penicillamine  gt  Cys  gt  GSH, respectively. Human serum albumin (HSA) carbonylation in the absence or presence of methylglyoxal scavengers were monitored by the determination of the amino, guanidine and thiol groups' contents, as well as by spectrofluorimetry, CD and native and SDS PAGE. Cys and penicillamine were highly efficient in the prevention of the carbonylation of the HSA-amino (for 80%) and guanidine (for 84% and 55%, respectively) groups and the formation of fluorescent AGEs. GSH and metformin exhibited medium efficiency (reduction of amino group's carbonylation for 60% and guanidine for about 30%); the least efficient was NAcCys. The presence of Cys, penicillamine and NAcCys led to an almost complete protection of the HSA-thiol group's carbonylation, whereas metformin was inefficient. The efficiency in the prevention of protein cross-linking increased in the order of metformin, NAcCys  lt  GSH  lt  penicillamine  lt  Cys. Thus, the substances with an alpha-amino-beta-mercapto-ethane group as a pharmacophore exhibit great potential as an efficient methylglyoxal scavengers, and are thus promising compounds for medicinal chemistry. In addition, they protect the HSA-SH group and preserve its antioxidative potential, which is very important for the HSA's function in vivo.
PB  - Royal Soc Chemistry, Cambridge
T2  - Molecular BioSystems
T1  - The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal
VL  - 10
IS  - 8
SP  - 2166
EP  - 2175
DO  - 10.1039/c4mb00217b
ER  - 
@article{
author = "Aćimović, Jelena M. and Penezić, Ana Z. and Pavićević, Ivan D. and Jovanović, Vesna B. and Mandić, Ljuba M.",
year = "2014",
abstract = "alpha-Oxoaldehydes, which are produced in higher quantities in diabetes, uremia, oxidative stress, inflammation and aging, react with the amino, guanidine and thiol groups of proteins and cause the formation of advanced glycated end-products and protein cross-linking. To prevent these reactions, the efficiency of tow molecular mass thiols with an alpha-amino-beta-mercapto-ethane group (Cys, penicillamine and N-acetylcysteine (NAcCys, with a blocked amino group)) as scavengers of methylglyoxal, compared with glutathione (GSH) and the biguanidine derivative metformin, was investigated. The time courses of the reactions of the aforementioned compounds with methylglyoxal were assayed. The reactivity of their thiol and amino groups decreased in the order of Cys  gt  penicillamine  gt  GSH  gt  NAcCys and penicillamine  gt  Cys  gt  GSH, respectively. Human serum albumin (HSA) carbonylation in the absence or presence of methylglyoxal scavengers were monitored by the determination of the amino, guanidine and thiol groups' contents, as well as by spectrofluorimetry, CD and native and SDS PAGE. Cys and penicillamine were highly efficient in the prevention of the carbonylation of the HSA-amino (for 80%) and guanidine (for 84% and 55%, respectively) groups and the formation of fluorescent AGEs. GSH and metformin exhibited medium efficiency (reduction of amino group's carbonylation for 60% and guanidine for about 30%); the least efficient was NAcCys. The presence of Cys, penicillamine and NAcCys led to an almost complete protection of the HSA-thiol group's carbonylation, whereas metformin was inefficient. The efficiency in the prevention of protein cross-linking increased in the order of metformin, NAcCys  lt  GSH  lt  penicillamine  lt  Cys. Thus, the substances with an alpha-amino-beta-mercapto-ethane group as a pharmacophore exhibit great potential as an efficient methylglyoxal scavengers, and are thus promising compounds for medicinal chemistry. In addition, they protect the HSA-SH group and preserve its antioxidative potential, which is very important for the HSA's function in vivo.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Molecular BioSystems",
title = "The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal",
volume = "10",
number = "8",
pages = "2166-2175",
doi = "10.1039/c4mb00217b"
}
Aćimović, J. M., Penezić, A. Z., Pavićević, I. D., Jovanović, V. B.,& Mandić, L. M.. (2014). The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal. in Molecular BioSystems
Royal Soc Chemistry, Cambridge., 10(8), 2166-2175.
https://doi.org/10.1039/c4mb00217b
Aćimović JM, Penezić AZ, Pavićević ID, Jovanović VB, Mandić LM. The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal. in Molecular BioSystems. 2014;10(8):2166-2175.
doi:10.1039/c4mb00217b .
Aćimović, Jelena M., Penezić, Ana Z., Pavićević, Ivan D., Jovanović, Vesna B., Mandić, Ljuba M., "The efficiency of compounds with alpha-amino-beta-mercapto-ethane group in protection of human serum albumin carbonylation and cross-linking with methylglyoxal" in Molecular BioSystems, 10, no. 8 (2014):2166-2175,
https://doi.org/10.1039/c4mb00217b . .
7
6
6
6

Improving the reliability of human serum albumin-thiol group determination

Jovanović, Vesna B.; Penezić-Romanjuk, Ana Z.; Pavićević, Ivan D.; Aćimović, Jelena M.; Mandić, Ljuba M.

(Academic Press Inc Elsevier Science, San Diego, 2013)

TY  - JOUR
AU  - Jovanović, Vesna B.
AU  - Penezić-Romanjuk, Ana Z.
AU  - Pavićević, Ivan D.
AU  - Aćimović, Jelena M.
AU  - Mandić, Ljuba M.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1369
AB  - The thiol (Cys34) content of human serum albumin (HSA-SH) decreases during oxidative and carbonyl stress and, therefore, could represent a useful parameter in clinical practice. Nevertheless, the reliability of HSA-thiol determination with Ellman's method depends on the purity of isolated HSA. Determination of total serum thiols (mmol/L) and HSA-SH content (mmol -SH/mmol HSA) after HSA isolation from diabetic patient and control sera by a two-step precipitation with ammonium sulfate (AS), as well as HSA-SH contribution (%) to total serum thiols, was assessed. Purity and yield of isolated HSA were monitored spectrophotometrically and by native polyacrylamide gel electrophoresis. Precipitation of HSA from serum via a two-step method with AS produced HSA with 91.9 +/- 3.6% purity and 69.7 +/- 4.4% yield, allowing for precise (relative standard deviation of 3.2%) and reliable (comparing with total serum thiols) measurement of HSA-SH content with DTNB [5,5'-dithiobis-(2-nitrobenzoic acid)]. The content of the HSA-SH group in patients with type 2 diabetes was significantly (P  lt  0.05) lower compared with that of the healthy cohort (0.483 +/- 0.067 vs. 0.561 +/- 0.054 mmol -SH/mmol HSA). Because the proposed method of HSA isolation is simple, time-efficient, and technically less demanding, and it also enables reliable determination of HSA-SH content, it is suitable for clinical practice.
PB  - Academic Press Inc Elsevier Science, San Diego
T2  - Analytical Biochemistry
T1  - Improving the reliability of human serum albumin-thiol group determination
VL  - 439
IS  - 1
SP  - 17
EP  - 22
DO  - 10.1016/j.ab.2013.03.033
ER  - 
@article{
author = "Jovanović, Vesna B. and Penezić-Romanjuk, Ana Z. and Pavićević, Ivan D. and Aćimović, Jelena M. and Mandić, Ljuba M.",
year = "2013",
abstract = "The thiol (Cys34) content of human serum albumin (HSA-SH) decreases during oxidative and carbonyl stress and, therefore, could represent a useful parameter in clinical practice. Nevertheless, the reliability of HSA-thiol determination with Ellman's method depends on the purity of isolated HSA. Determination of total serum thiols (mmol/L) and HSA-SH content (mmol -SH/mmol HSA) after HSA isolation from diabetic patient and control sera by a two-step precipitation with ammonium sulfate (AS), as well as HSA-SH contribution (%) to total serum thiols, was assessed. Purity and yield of isolated HSA were monitored spectrophotometrically and by native polyacrylamide gel electrophoresis. Precipitation of HSA from serum via a two-step method with AS produced HSA with 91.9 +/- 3.6% purity and 69.7 +/- 4.4% yield, allowing for precise (relative standard deviation of 3.2%) and reliable (comparing with total serum thiols) measurement of HSA-SH content with DTNB [5,5'-dithiobis-(2-nitrobenzoic acid)]. The content of the HSA-SH group in patients with type 2 diabetes was significantly (P  lt  0.05) lower compared with that of the healthy cohort (0.483 +/- 0.067 vs. 0.561 +/- 0.054 mmol -SH/mmol HSA). Because the proposed method of HSA isolation is simple, time-efficient, and technically less demanding, and it also enables reliable determination of HSA-SH content, it is suitable for clinical practice.",
publisher = "Academic Press Inc Elsevier Science, San Diego",
journal = "Analytical Biochemistry",
title = "Improving the reliability of human serum albumin-thiol group determination",
volume = "439",
number = "1",
pages = "17-22",
doi = "10.1016/j.ab.2013.03.033"
}
Jovanović, V. B., Penezić-Romanjuk, A. Z., Pavićević, I. D., Aćimović, J. M.,& Mandić, L. M.. (2013). Improving the reliability of human serum albumin-thiol group determination. in Analytical Biochemistry
Academic Press Inc Elsevier Science, San Diego., 439(1), 17-22.
https://doi.org/10.1016/j.ab.2013.03.033
Jovanović VB, Penezić-Romanjuk AZ, Pavićević ID, Aćimović JM, Mandić LM. Improving the reliability of human serum albumin-thiol group determination. in Analytical Biochemistry. 2013;439(1):17-22.
doi:10.1016/j.ab.2013.03.033 .
Jovanović, Vesna B., Penezić-Romanjuk, Ana Z., Pavićević, Ivan D., Aćimović, Jelena M., Mandić, Ljuba M., "Improving the reliability of human serum albumin-thiol group determination" in Analytical Biochemistry, 439, no. 1 (2013):17-22,
https://doi.org/10.1016/j.ab.2013.03.033 . .
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Chronic isolation stress compromises JNK/c-Jun signaling in rat brain

Filipović, Dragana; Zlatkovic, Jelena; Pavićević, Ivan D.; Mandić, Ljuba M.; Demajo, Miroslav

(Springer Wien, Wien, 2012)

TY  - JOUR
AU  - Filipović, Dragana
AU  - Zlatkovic, Jelena
AU  - Pavićević, Ivan D.
AU  - Mandić, Ljuba M.
AU  - Demajo, Miroslav
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1540
AB  - The c-Jun NH2-terminal kinases (JNKs) are important stress-responsive kinases. They regulate cellular activities by sequential phosphorylation and activation through a mitogen-activated protein kinase cascade, whereas JNKs activation is altered in response to various stressors. In the present study, we used immunoblotting to assess the effect of 21 day of social isolation as the chronic stressor, either sole and in combination with 2 h of acute immobilization or cold (4A degrees C) stress on circulating corticosterone level and phosphorylation status of p46 (phospho-p46/total p46) and p54 (phospho-p54/total p54) JNK isoforms in the cytosolic and nuclear fraction of the prefrontal cortex and hippocampus of male Wistar rats. Also, the phosphorylation status of JNK nuclear down-stream target c-Jun (p-c-Jun/c-Jun) on Ser63 was examined. Both acute stressors with elevated CORT levels led to increased phosphorylation status of cytosolic p54 JNK isoforms but not p46 JNK isoforms only in the hippocampus and no change in phosphorylation status of c-jun in both brain regions. Chronic isolation with unaltered CORT level and reduced responsiveness to novel acute stressors, led to unchanged or reduced phosphorylation status of p46 and p54 JNK isoforms in both fractions and both brain regions, whereas the decrease of c-Jun phosphorylation status was found only in the prefrontal cortex. Our results suggest that compromised JNKs activation following chronic isolation may lead to interruption of JNK signaling, which could be related with neuropsychiatric disorders such as depression or long-lasting neuronal remodeling.
PB  - Springer Wien, Wien
T2  - Journal of Neural Transmission
T1  - Chronic isolation stress compromises JNK/c-Jun signaling in rat brain
VL  - 119
IS  - 11
SP  - 1275
EP  - 1284
DO  - 10.1007/s00702-012-0776-0
ER  - 
@article{
author = "Filipović, Dragana and Zlatkovic, Jelena and Pavićević, Ivan D. and Mandić, Ljuba M. and Demajo, Miroslav",
year = "2012",
abstract = "The c-Jun NH2-terminal kinases (JNKs) are important stress-responsive kinases. They regulate cellular activities by sequential phosphorylation and activation through a mitogen-activated protein kinase cascade, whereas JNKs activation is altered in response to various stressors. In the present study, we used immunoblotting to assess the effect of 21 day of social isolation as the chronic stressor, either sole and in combination with 2 h of acute immobilization or cold (4A degrees C) stress on circulating corticosterone level and phosphorylation status of p46 (phospho-p46/total p46) and p54 (phospho-p54/total p54) JNK isoforms in the cytosolic and nuclear fraction of the prefrontal cortex and hippocampus of male Wistar rats. Also, the phosphorylation status of JNK nuclear down-stream target c-Jun (p-c-Jun/c-Jun) on Ser63 was examined. Both acute stressors with elevated CORT levels led to increased phosphorylation status of cytosolic p54 JNK isoforms but not p46 JNK isoforms only in the hippocampus and no change in phosphorylation status of c-jun in both brain regions. Chronic isolation with unaltered CORT level and reduced responsiveness to novel acute stressors, led to unchanged or reduced phosphorylation status of p46 and p54 JNK isoforms in both fractions and both brain regions, whereas the decrease of c-Jun phosphorylation status was found only in the prefrontal cortex. Our results suggest that compromised JNKs activation following chronic isolation may lead to interruption of JNK signaling, which could be related with neuropsychiatric disorders such as depression or long-lasting neuronal remodeling.",
publisher = "Springer Wien, Wien",
journal = "Journal of Neural Transmission",
title = "Chronic isolation stress compromises JNK/c-Jun signaling in rat brain",
volume = "119",
number = "11",
pages = "1275-1284",
doi = "10.1007/s00702-012-0776-0"
}
Filipović, D., Zlatkovic, J., Pavićević, I. D., Mandić, L. M.,& Demajo, M.. (2012). Chronic isolation stress compromises JNK/c-Jun signaling in rat brain. in Journal of Neural Transmission
Springer Wien, Wien., 119(11), 1275-1284.
https://doi.org/10.1007/s00702-012-0776-0
Filipović D, Zlatkovic J, Pavićević ID, Mandić LM, Demajo M. Chronic isolation stress compromises JNK/c-Jun signaling in rat brain. in Journal of Neural Transmission. 2012;119(11):1275-1284.
doi:10.1007/s00702-012-0776-0 .
Filipović, Dragana, Zlatkovic, Jelena, Pavićević, Ivan D., Mandić, Ljuba M., Demajo, Miroslav, "Chronic isolation stress compromises JNK/c-Jun signaling in rat brain" in Journal of Neural Transmission, 119, no. 11 (2012):1275-1284,
https://doi.org/10.1007/s00702-012-0776-0 . .
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