Article ID Journal Published Year Pages File Type
1199577 Journal of Chromatography A 2014 8 Pages PDF
Abstract

•A vorinostat-based small molecule probe was designed, synthesized and immobilized onto the surface of sepharose beads.•Vorinosta-coated beads based proteomics approach for profiling of novel target proteins of vorinostat.•ENO-1 was detected and confirmed as a novel, potential target of vorinostat.

Inhibitors of histone deacetylases (HDACs) have been considered to be new anticancer agents. As a key inhibitor of HDAC, vorinostat can cause growth arrest and death of a broad of transformed cells and interact with a variety of substrates. A comprehensive analysis of proteins interacting with HDAC inhibitors is of great importance in understanding molecular mechanisms of the drugs. Here, we reported the preparation and characterization of vorinostat-coated beads for profiling of novel target proteins of vorinostat (a key HDAC inhibitor). The enriched proteins were further analyzed by HPLC–MS/MS. Besides the known substrates, there were also several novel enriched protein candidates, one of which was a metalloenzyme α-enolase (ENO-1). According to our best knowledge, it is the first time that ENO-1 has been detected as a potential target of vorinostat through chemoproteomics approach. Further competition analysis indicated that ENO-1 may be co-enriched as a substrate complex. Our results demonstrated that the chemical probe combined with proteomics approach may be developed as a potential tool to identify target proteins of drugs.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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