1. Academic Validation
  2. Gut Microbial β-Glucuronidase Inhibition via Catalytic Cycle Interception

Gut Microbial β-Glucuronidase Inhibition via Catalytic Cycle Interception

  • ACS Cent Sci. 2018 Jul 25;4(7):868-879. doi: 10.1021/acscentsci.8b00239.
Samuel J Pellock 1 Benjamin C Creekmore 1 William G Walton 1 Naimee Mehta 1 Kristen A Biernat 1 Andrew P Cesmat 1 Yamuna Ariyarathna 1 Zachary D Dunn 1 Bo Li 1 Jian Jin 2 Lindsey I James 1 Matthew R Redinbo 1 1
Affiliations

Affiliations

  • 1 Department of Chemistry, Center for Integrated Chemical Biology and Drug Discovery, Eshelman School of Pharmacy, and Integrated Program for Biological and Genome Sciences, and Departments of Biochemistry and Microbiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
  • 2 Department of Pharmacological Sciences, Icahn School of Medicine at Mt. Sinai, New York, New York 10029, United States.
Abstract

Microbial β-glucuronidases (GUSs) cause severe gut toxicities that limit the efficacy of Cancer drugs and other therapeutics. Selective inhibitors of Bacterial GUS have been shown to alleviate these side effects. Using structural and chemical biology, mass spectrometry, and cell-based assays, we establish that piperazine-containing GUS inhibitors intercept the glycosyl-enzyme catalytic intermediate of these retaining glycosyl hydrolases. We demonstrate that piperazine-based compounds are substrate-dependent GUS inhibitors that bind to the GUS-GlcA catalytic intermediate as a piperazine-linked glucuronide (GlcA, glucuronic acid). We confirm the GUS-dependent formation of inhibitor-glucuronide conjugates by LC-MS and show that methylated piperazine analogs display significantly reduced potencies. We further demonstrate that a range of approved piperazine- and piperidine-containing drugs from many classes, including those for the treatment of depression, Infection, and Cancer, function by the same mechanism, and we confirm through gene editing that these compounds selectively inhibit GUS in living Bacterial cells. Together, these data reveal a unique mechanism of GUS inhibition and show that a range of therapeutics may impact GUS activities in the human gut.

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