结核分枝杆菌
毒力
蛋白质酪氨酸磷酸酶
毒力因子
微生物学
肺结核
磷酸酶
磺胺
分枝杆菌
作用机理
生物
化学
酶
生物化学
医学
立体化学
基因
体外
病理
作者
Lan Chen,Bo Zhou,Sheng Zhang,Li Wu,Yuehong Wang,Scott G. Franzblau,Zhong‐Yin Zhang
摘要
Mycobacterium protein tyrosine phosphatase B (mPTPB) is an essential virulence factor required for Mycobacterium tuberculosis (Mtb) survival in host macrophages. Consequently, mPTPB represents an exciting new target with a completely novel mechanism of action. We screened a library of 7,500 compounds against mPTPB and identified several 2-oxo-1,2-dihydrobenzo[cd]indole-6-sulfonamide and piperazinyl-thiophenyl-ethyl-oxalamide derivatives as two distinct classes of mPTPB inhibitors. We showed that both classes of inhibitors are capable of blocking the mPTPB-mediated ERK1/2 inactivation. We further demonstrated that both classes of mPTPB inhibitors are effective in inhibiting the growth of Mtb in macrophages. Thus, improvement of the lead compounds may produce a novel class of anti-TB agents.
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