Glucose autoxidation induces functional damage to proteins via modification of critical arginine residues

Sergei Chetyrkin, Missy Mathis, Vadim Pedchenko, Otto A. Sanchez, W. Hayes McDonald, David L. Hachey, Hartman Madu, Donald Stec, Billy Hudson, Paul Voziyan

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

Nonenzymatic modification of proteins in hyperglycemia is a major mechanism causing diabetic complications. These modifications can have pathogenic consequences when they target active site residues, thus affecting protein function. In the present study, we examined the role of glucose autoxidation in functional protein damage using lysozyme and RGD-α3NC1 domain of collagen IV as model proteins in vitro. We demonstrated that glucose autoxidation induced inhibition of lysozyme activity as well as NC1 domain binding to αVβ3 integrin receptor via modification of critical arginine residues by reactive carbonyl species (RCS) glyoxal (GO) and methylglyoxal while nonoxidative glucose adduction to the protein did not affect protein function. The role of RCS in protein damage was confirmed using pyridoxamine which blocked glucose autoxidation and RCS production, thus protecting protein function, even in the presence of high concentrations of glucose. Glucose autoxidation may cause protein damage in vivo since increased levels of GO-derived modifications of arginine residues were detected within the assembly interface of collagen IV NC1 domains isolated from renal ECM of diabetic rats. Since arginine residues are frequently present within protein active sites, glucose autoxidation may be a common mechanism contributing to ECM protein functional damage in hyperglycemia and oxidative environment. Our data also point out the pitfalls in functional studies, particularly in cell culture experiments, that involve glucose treatment but do not take into account toxic effects of RCS derived from glucose autoxidation.

Original languageEnglish (US)
Pages (from-to)6102-6112
Number of pages11
JournalBiochemistry
Volume50
Issue number27
DOIs
StatePublished - Jul 12 2011

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