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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10396300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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