Loading…

In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate

► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate. Amino groups in proteins can non-enzymatically react with reducing su...

Full description

Saved in:
Bibliographic Details
Published in:Biochemical and biophysical research communications 2012-01, Vol.417 (2), p.817-823
Main Authors: Seneviratne, Champika, Dombi, G.W., Liu, W., Dain, J.A.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate. Amino groups in proteins can non-enzymatically react with reducing sugars to generate a structurally diverse group of compounds referred to as advanced glycation end products (AGEs). The in vivo formation of AGEs contributes to some of the complications of diabetes including atherosclerosis, cataract formation, and renal failure. The formation of AGEs is dependent on both sugar and protein concentrations. Increases in temperature, pH, and exposure time of sugars to the proteins also play a significant role in the rate of AGE formation. This study focuses on the use of a combination of analytical techniques to study the in vitro AGE formation of HSA with dihydroxyacetone phosphate (DHAP), a ketose generated during glycolysis, and its dephosphorylated analog, dihydroxy acetone (DHA), commonly used as a browning reagent in skin tanning preparations. The extent of AGE formation was affected by DHAP and DHA concentrations and by the duration of HSA exposure to these glycating agents. Increases in temperature and pH sped the glycation process and enhanced the formation of the AGEs of HSA. MALDI-TOF mass spectroscopic data provided a reliable result to evaluate the extent of the AGE formation.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2011.12.043