A Whole Proteome Inventory of Background Photocrosslinker Binding

  • Philipp Kleiner
  • , Wolfgang Heydenreuter
  • , Matthias Stahl
  • , Vadim S. Korotkov
  • , Stephan A. Sieber

Research output: Contribution to journalArticlepeer-review

97 Scopus citations

Abstract

Affinity-based protein profiling (AfBPP) is a widely applied method for the target identification of bioactive molecules. Probes containing photocrosslinkers, such as benzophenones, diazirines, and aryl azides, irreversibly link the molecule of interest to its target protein upon irradiation with UV light. Despite their prevalent application, little is known about photocrosslinker-specific off-targets, affecting the reliability of results. Herein, we investigated background protein labeling by gel-free quantitative proteomics. Characteristic off-targets were identified for each photoreactive group and compiled in a comprehensive inventory. In a proof-of-principle study, H8, a protein kinase A inhibitor, was equipped with a diazirine moiety. Application of this photoprobe revealed, by alignment with the diazirine background, unprecedented insight into its in situ proteome targets. Taken together, our findings guide the identification of biologically relevant binders in photoprobe experiments.

Original languageEnglish
Pages (from-to)1396-1401
Number of pages6
JournalAngewandte Chemie International Edition in English
Volume56
Issue number5
DOIs
StatePublished - 24 Jan 2017

Keywords

  • enzymes
  • photoaffinity labeling
  • photoreactive probes
  • protein profiling
  • proteomics

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