Comparison of glycation of glutathione S-transferase by methylglyoxal, glucose or fructose

Molecular and Cellular Biochemistry

Volumn 357, Issue 1-2, 2011, Pages 323-330

  Boušová, Iva ^a   Průchová, Zuzana ^a   Trnková, Lucie ^a,b   Dršata, Jaroslav ^a  

^a Charles University in Prague Faculty of Pharmacy   (Czech Republic)

^b UNIVERSITY OF HRADEC KRALOVE   (Czech Republic)

Author keywords

Advanced glycation end products; Glutathione S transferase; Methylglyoxal; Protein conformation; Protein glycation

Indexed keywords

AMINE; FRUCTOSE; GLUCOSE; GLUTATHIONE TRANSFERASE; METHYLGLYOXAL; ADVANCED GLYCATION END PRODUCT; XENOBIOTIC AGENT;

ARTICLE; ENZYME ACTIVITY; FLUORESCENCE IMAGING; GLYCATION; IN VITRO STUDY; MOLECULAR WEIGHT; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN AGGREGATION; PROTEIN CONFORMATION; PROTEIN CONTENT; PROTEIN CROSS LINKING; PROTEIN MODIFICATION; WESTERN BLOTTING; AGING; ANIMAL; CATALYSIS; CHEMISTRY; COMPARATIVE STUDY; DIABETES MELLITUS; ENZYMOLOGY; HUMAN; METABOLISM;

AGING; ANIMALS; CATALYSIS; DIABETES MELLITUS; FRUCTOSE; GLUCOSE; GLUTATHIONE TRANSFERASE; GLYCOSYLATION END PRODUCTS, ADVANCED; HUMANS; PYRUVALDEHYDE; XENOBIOTICS;

EID: 84857431411     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-011-0903-5     Document Type: Article

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