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Characterizing harmful advanced glycation end-products (AGEs) and ribosylated aggregates of yellow mustard seed phytocystatin: Effects of different monosaccharides
Journal article   Peer reviewed

Characterizing harmful advanced glycation end-products (AGEs) and ribosylated aggregates of yellow mustard seed phytocystatin: Effects of different monosaccharides

Azaj Ahmed, Anas Shamsi and Bilqees Bano
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, Vol.171, pp.183-192
01/15/2017
DOI: 10.1016/j.saa.2016.08.004
PMID: 27526342

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Abstract

Advanced glycation end products (AGEs) are at the core of variety of diseases ranging from diabetes to renal failure and hence gaining wide consideration. This study was aimed at characterizing the AGEs of phytocystatin isolated from mustard seeds (YMP) when incubated with different monosaccharides (glucose, ribose and mannose) using fluorescence, ultraviolet, circular dichroism (CD) spectroscopy and microscopy. Ribose was found to be the most potent glycating agent as evident by AGEs specific fluorescence and absorbance. YMP exists as a molten globule like structure on day 24 as depicted by high ANS fluorescence and altered intrinsic fluorescence. Glycated YMP as AGEs and ribose induced aggregates were observed at day 28 and 32 respectively. In our study we have also examined the anti-aggregative potential of polyphenol, resveratrol. Our results suggested the anti-aggregative behavior of resveratrol as it prevented the in vitro aggregation of YMP, although further studies are required to decode the mechanism by which resveratrol prevents the aggregation.
Circular Dichroism Comet Assay Congo Red - chemistry Cystatins - chemistry Cystatins - ultrastructure Glycation End Products, Advanced - chemistry Glycosylation Monosaccharides - chemistry Mustard Plant - chemistry Nephelometry and Turbidimetry Papain - antagonists & inhibitors Protein Aggregates Protein Structure, Secondary Protein Structure, Tertiary Ribose - chemistry Seeds - chemistry Spectrometry, Fluorescence Spectrophotometry, Ultraviolet Thiazoles - chemistry

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