Activity-based lipid esterase profi ling of m. Bovis BCG at different metabolic states using tetrahydrolipstatin (THL) as bait

Madhu Sudhan Ravindran, Markus R. Wenk*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

3 Citations (Scopus)

Abstract

This chapter provides a step-by-step protocol using activity-based protein profiling (ABPP) as a chemicalproteomic tool to survey the antibiotic properties of a small molecule. Here, we investigate the molecular mechanism behind the bactericidal activity of tetrahydrolipstatin (THL). ABPP relies on small molecule probes that target the active site of specific enzymes in complex proteomes. These probes in turn are equipped with a reporter tag that allows capturing, visualization, enrichment, identifi cation, and quantify cation of its targets either in vitro or in situ. THL possesses bactericidal activities, but its precise spectrum of molecular targets is poorly characterized. Here, we used THL analogs functionalized to enable Huisgen-base cycloaddition, commonly known as “click chemistry,” to identify target proteins after enrichment from mycobacteria cell lysates obtained from different physiological conditions.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages75-85
Number of pages11
DOIs
Publication statusPublished - 2017
Externally publishedYes

Publication series

NameMethods in Molecular Biology
Volume1491
ISSN (Print)1064-3745

Keywords

  • Activity-based protein profi ling
  • Cycloaddition reaction
  • Lipases
  • Lipid esterases
  • Tetrahydrolipstatin

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