Identification of the Binding Site of Chroman-4-one-Based Sirtuin 2-Selective Inhibitors using Photoaffinity Labeling in Combination with Tandem Mass Spectrometry

摘要

Photoaffinity labeling (PAL) was used to identify the binding site of chroman-4-one-based SIRT2-selective inhibitors. The photoactive diazirine 4, a potent SIRT2 inhibitor, was subjected to detailed photochemical characterization. In PAL experiments with SIRT2, a tryptic peptide originating from the covalent attachment of photo activated 4 was identified. The peptide covers both the active site of SIRT2 and the proposed binding site of chroman-4one-based inhibitors. A high-power LED was used as source for the monochromatic UV light enabling rapid photo activation.