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

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 opp...

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Autores principales: Salas-Lloret, Daniel, Jansen, Nicolette S., Nagamalleswari, Easa, van der Meulen, Coen, Gracheva, Ekaterina, de Ru, Arnoud H., Otte, H. Anne Marie, van Veelen, Peter A., Pichler, Andrea, Goedhart, Joachim, Vertegaal, Alfred C.O., González-Prieto, Román
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10396300/
https://www.ncbi.nlm.nih.gov/pubmed/37531430
http://dx.doi.org/10.1126/sciadv.adh2073
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author Salas-Lloret, Daniel
Jansen, Nicolette S.
Nagamalleswari, Easa
van der Meulen, Coen
Gracheva, Ekaterina
de Ru, Arnoud H.
Otte, H. Anne Marie
van Veelen, Peter A.
Pichler, Andrea
Goedhart, Joachim
Vertegaal, Alfred C.O.
González-Prieto, Román
author_facet Salas-Lloret, Daniel
Jansen, Nicolette S.
Nagamalleswari, Easa
van der Meulen, Coen
Gracheva, Ekaterina
de Ru, Arnoud H.
Otte, H. Anne Marie
van Veelen, Peter A.
Pichler, Andrea
Goedhart, Joachim
Vertegaal, Alfred C.O.
González-Prieto, Román
author_sort Salas-Lloret, Daniel
collection PubMed
description 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.
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spelling pubmed-103963002023-08-03 SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome Salas-Lloret, Daniel Jansen, Nicolette S. Nagamalleswari, Easa van der Meulen, Coen Gracheva, Ekaterina de Ru, Arnoud H. Otte, H. Anne Marie van Veelen, Peter A. Pichler, Andrea Goedhart, Joachim Vertegaal, Alfred C.O. González-Prieto, Román Sci Adv Biomedicine and Life Sciences 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. American Association for the Advancement of Science 2023-08-02 /pmc/articles/PMC10396300/ /pubmed/37531430 http://dx.doi.org/10.1126/sciadv.adh2073 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Salas-Lloret, Daniel
Jansen, Nicolette S.
Nagamalleswari, Easa
van der Meulen, Coen
Gracheva, Ekaterina
de Ru, Arnoud H.
Otte, H. Anne Marie
van Veelen, Peter A.
Pichler, Andrea
Goedhart, Joachim
Vertegaal, Alfred C.O.
González-Prieto, Román
SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title_full SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title_fullStr SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title_full_unstemmed SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title_short SUMO-activated target traps (SATTs) enable the identification of a comprehensive E3-specific SUMO proteome
title_sort sumo-activated target traps (satts) enable the identification of a comprehensive e3-specific sumo proteome
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10396300/
https://www.ncbi.nlm.nih.gov/pubmed/37531430
http://dx.doi.org/10.1126/sciadv.adh2073
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