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Chembiochem. 2017 May 18;18(10):931-940. doi: 10.1002/cbic.201600655. Epub 2017 Apr 18.

Studies of the Binding of Modest Modulators of the Human Enzyme, Sirtuin 6, by STD NMR.

Author information

1
Department of Chemistry, University at Albany, 1400 Washington Avenue, Albany, NY, 12205, USA.

Abstract

Pyrazinamide (PZA), an essential constituent of short-course tuberculosis chemotherapy, binds weakly but selectively to Sirtuin 6 (SIRT6). Despite the structural similarities between nicotinamide (NAM), PZA, and pyrazinoic acid (POA), these inhibitors modulate SIRT6 by different mechanisms and through different binding sites, as suggested by saturation transfer difference (STD) NMR. Available experimental evidence, such as that derived from crystal structures and kinetic experiments, has been of only limited utility in elucidation of the mechanistic details of sirtuin inhibition by NAM or other inhibitors. For instance, crystallographic structural analysis of sirtuin binding sites does not help us understand important differences in binding affinities among sirtuins or capture details of such dynamic process. Hence, STD NMR was utilized throughout this study. Our results not only agreed with the binding kinetics experiments but also gave a qualitative insight into the binding process. The data presented herein suggested some details about the geometry of the binding epitopes of the ligands in solution with the apo- and holoenzyme. Recognition that SIRT6 is affected selectively by PZA, an established clinical agent, suggests that the rational development of more potent and selective NAM surrogates might be possible. These derivatives might be accessible by employing the malleability of this scaffold to assist in the identification by STD NMR of the motifs that interact with the apo- and holoenzymes in solution.

KEYWORDS:

NAD+; SIRT6; STD-NMR; nicotinamide; pyrazinamide

PMID:
28222243
DOI:
10.1002/cbic.201600655
[Indexed for MEDLINE]

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