Abstract
The effects of beta-cyclodextrin (beta-CyD) and trehalose on glycation of human serum albumin (HSA) were studied. These additives reduced AGEs and nanofibril formation of HSA under in vitro glycation conditions and improved its helical structure. These were accomplished through direct interactions of them with HSA and alterations in solute-protein interactions.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Circular Dichroism
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Glucose / metabolism
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Glycation End Products, Advanced / metabolism*
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Glycosylation
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Humans
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Serum Albumin / metabolism*
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Solubility
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Spectrometry, Fluorescence
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Trehalose / pharmacology*
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beta-Cyclodextrins / pharmacology*
Substances
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Glycation End Products, Advanced
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Serum Albumin
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beta-Cyclodextrins
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Trehalose
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Glucose
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betadex