Competitive ABPP of Serine Hydrolases: A Case Study on DAGL-Alpha

Marc P Baggelaar*, Mario Van der Stelt*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Competitive activity-based protein profiling is a highly efficient chemical biology technique to determine target engagement and selectivity profiles of enzyme inhibitors in complex proteomes. Fluorophosphonate-based fluorescent inhibitors are widely used as broad-spectrum probes for serine hydrolases. However, diacylglycerol lipase-α is not labeled by fluorophosphonate-based probes. To overcome this problem, we have developed a tailor-made activity-based probe that reacts with diacylglycerol lipase-α. Here we describe a case study in which we apply competitive activity-based protein profiling using a broad-spectrum and a tailor-made activity-based probe to establish selectivity and activity profiles of inhibitors targeting diacylglycerol lipase-α in the mouse brain proteome.

Original languageEnglish
Pages (from-to)161-169
Number of pages9
JournalMethods in Molecular Biology
Volume1491
DOIs
Publication statusPublished - 2017
Externally publishedYes

Keywords

  • Animals
  • Brain/enzymology
  • Hydrolases/chemistry
  • Lipoprotein Lipase/metabolism
  • Mice
  • Proteome
  • Serine/chemistry

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