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

Authors :
Salas-Lloret D
Jansen NS
Nagamalleswari E
van der Meulen C
Gracheva E
de Ru AH
Otte HAM
van Veelen PA
Pichler A
Goedhart J
Vertegaal ACO
González-Prieto R
Source :
Science advances [Sci Adv] 2023 Aug 02; Vol. 9 (31), pp. eadh2073. Date of Electronic Publication: 2023 Aug 02.
Publication Year :
2023

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.

Details

Language :
English
ISSN :
2375-2548
Volume :
9
Issue :
31
Database :
MEDLINE
Journal :
Science advances
Publication Type :
Academic Journal
Accession number :
37531430
Full Text :
https://doi.org/10.1126/sciadv.adh2073