Two-Way Regulation of MmpL3 Expression Identifies and Validates Inhibitors of MmpL3 Function in Mycobacterium tuberculosis Articles uri icon

authors

  • GROVER, SHIPRA
  • ENGELHART, CURTIS A.
  • PEREZ HERRANZ, ESTHER
  • LI, WEI
  • ABRAHAMS, KATHERINE A.
  • PAPAVINASASUNDARAM, KADAMBA
  • BEAN, JAMES M.
  • SASSETTI, CHRISTOPHER M.
  • MENDOZA LOSANA, ALFONSO
  • BESRA, GURDYAL S.
  • JACKSON, MARY
  • SCHNAPPINGER, DIRK

publication date

  • January 2021

start page

  • 141

end page

  • 152

issue

  • 1

volume

  • 7

International Standard Serial Number (ISSN)

  • 2373-8227

abstract

  • MmpL3, an essential mycolate transporter in the inner membrane of Mycobacterium tuberculosis (Mtb), has been identified as a target of multiple, chemically diverse antitubercular drugs. However, several of these molecules seem to have secondary targets and inhibit bacterial growth by more than one mechanism. Here, we describe a cell-based assay that utilizes two-way regulation of MmpL3 expression to readily identify MmpL3-specific inhibitors. We successfully used this assay to identify a novel guanidine-based MmpL3 inhibitor from a library of 220 compounds that inhibit growth of Mtb by largely unknown mechanisms. We furthermore identified inhibitors of cytochrome bc1-aa3 oxidase as one class of off-target hits in whole-cell screens for MmpL3 inhibitors and report a novel sulfanylacetamide as a potential QcrB inhibitor.

subjects

  • Biology and Biomedicine

keywords

  • targetedwhole-cellscreen; mycolicacids; antibiotics; moleculargenetics; drugdiscovery; respiration