Catalysis and mechanistic insights into sirtuin activation

KE Dittenhafer‐Reed, JL Feldman, JM Denu - Chembiochem, 2011 - Wiley Online Library
KE Dittenhafer‐Reed, JL Feldman, JM Denu
Chembiochem, 2011Wiley Online Library
SIRT1 is a member of the Sir2 family of NAD+‐dependent protein deacetylases. The central
role of SIRT1 in multiple metabolic and age‐related pathways has pushed SIRT1 to the
forefront to discover small‐molecule activators. Promising compounds, including resveratrol
and SRT1720 have been reported, however, whether these compounds are direct activators
and the mechanism by which they activate remains poorly defined. This review examines
the current debate surrounding purported activators, and will focus on the assays used in …
Abstract
SIRT1 is a member of the Sir2 family of NAD+‐dependent protein deacetylases. The central role of SIRT1 in multiple metabolic and age‐related pathways has pushed SIRT1 to the forefront to discover small‐molecule activators. Promising compounds, including resveratrol and SRT1720 have been reported, however, whether these compounds are direct activators and the mechanism by which they activate remains poorly defined. This review examines the current debate surrounding purported activators, and will focus on the assays used in screening compounds, sirtuin catalysis, and the mechanistic basis for their actions. We discuss the potential pathways of SIRT1 activation that could be exploited for the development of novel therapeutics for treating type II diabetes, neurodegeneration, and diseases associated with aging.
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