Abstract

Protein tyrosine phosphatase B (PtpB) is one of the virulence factors secreted into the host cell by Mycobacterium tuberculosis. PtpB attenuates host immune defenses by interfering with signal transduction pathways in macrophages and, therefore, it is considered a promising target for the development of novel anti-tuberculosis drugs. Here we report the discovery of natural compound inhibitors of PtpB among an in house library of more than 800 natural substances by means of a multidisciplinary approach, mixing in silico screening with enzymatic and kinetics studies and MS assays. Six natural compounds proved to inhibit PtpB at low micromolar concentrations (< 30 µM) with Kuwanol E being the most potent with K i = 1.6 ± 0.1 µM. To the best of our knowledge, Kuwanol E is the most potent natural compound PtpB inhibitor reported so far, as well as it is the first non-peptidic PtpB inhibitor discovered from natural sources. Compounds herein identified may inspire the design of novel specific PtpB inhibitors.

Highlights

  • Tuberculosis (TB) kills nearly 2 million people annually

  • In previous studies we evaluated the capability of the Molecular Mechanics Generalized Born Surface Area (MM-GBSA) method in rescoring docking poses generated with GOLD [41,48]

  • In this work we reported on the discovery of natural compounds as potent inhibitors of Protein tyrosine phosphatase B (PtpB) by in silico screening of an in house unique library and enzymatic assays

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Summary

Introduction

Tuberculosis (TB) kills nearly 2 million people annually. The World Health Organization (WHO) declared TB as a global health emergency, which highlights the importance of TB as a major threat to humans [1]. Drug resistance and patient noncompliance are two key factors that affect the success rate of conventional treatments against TB. Exoenzymes protein tyrosine phosphatase A (PtpA) and B (PtpB) have emerged as promising therapeutic targets to discover new anti-TB agents [2,3,4,5]. These enzymes are secreted into the host cell by Mycobacterium tuberculosis (Mtb) and attenuate host immune defenses by interfering with the host signaling pathways [6,7]

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