Mass spectrometry (MS)-based ubiquitinomics allows a system-level understanding of ubiquitin signaling.

In this publication, we focus on:

  • A background to ubiquitinome profiling
  • Presentation of a scalable and robust workflow for deep and precise in vivo ubiquitinome profiling using DIA-MS (data-independent acquisition mass spectrometry) and neural network based data processing
  • Comprehensive mapping of substrates of deubiquitinase USP7, an anticancer drug target known to regulate tumor suppressor p53
  • Application of the method including rapid mode of action profiling of candidate drugs targeting deubiquitinases or ubiquitin ligases

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