SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome

Open Access
Authors
  • D. Salas-Lloret
  • N.S. Jansen
  • E. Nagamalleswari
  • C. van der Meulen
  • E. Gracheva
  • A.H. de Ru
  • H.A.M. Otte
  • P.A. van Veelen
  • A. Pichler
  • J. Goedhart ORCID logo
  • A.C.O. Vertegaal
  • R. González-Prieto
Publication date 04-08-2023
Journal Science Advances
Article number eadh2073
Volume | Issue number 9 | 31
Number of pages 16
Organisations
  • Faculty of Science (FNWI) - Swammerdam Institute for Life Sciences (SILS)
Abstract
Ubiquitin and ubiquitin-like conjugation cascades consist of dedicated E1, E2, and E3 enzymes with E3s providing substrate specificity. Mass spectrometry-based approaches have enabled the identification of more than 6500 SUMO2/3 target proteins. The limited number of SUMO E3s provides the unique opportunity to systematically study E3 substrate wiring. We developed SUMO-activated target traps (SATTs) and systematically identified substrates for eight different SUMO E3s, PIAS1, PIAS2, PIAS3, PIAS4, NSMCE2, ZNF451, LAZSUL (ZNF451-3), and ZMIZ2. SATTs enabled us to identify 427 SUMO1 and 961 SUMO2/3 targets in an E3-specific manner. We found pronounced E3 substrate preference. Quantitative proteomics enabled us to measure substrate specificity of E3s, quantified using the SATT index. Furthermore, we developed the Polar SATTs web-based tool to browse the dataset in an interactive manner. Overall, we uncover E3-to-target wiring of 1388 SUMO substrates, highlighting unique and overlapping sets of substrates for eight different SUMO E3 ligases.
Document type Article
Language English
Published at https://doi.org/10.1126/sciadv.adh2073
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SUMO-activated target traps (SATTs) (Final published version)
Supplementary materials
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