结核分枝杆菌
蛋白质酪氨酸磷酸酶
生物信息学
化学
肺结核
酶
磷酸酶
毒力
生物化学
医学
基因
病理
作者
Alessandra Mascarello,Mattia Mori,Louise Domeneghini Chiaradia-Delatorre,Angela Camila Orbem Menegatti,Franco Delle Monachè,Franco Ferrari,Rosendo Augusto Yunes,Ricardo J. Nunes,Hernán Terenzi,Bruno Botta,Maurizio Botta
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2013-10-14
卷期号:8 (10): e77081-e77081
被引量:58
标识
DOI:10.1371/journal.pone.0077081
摘要
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.
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