Identification of proximal SUMO-dependent interactors using SUMO-ID.
Cell Line, Tumor
GTPase-Activating Proteins
/ metabolism
HEK293 Cells
Humans
Promyelocytic Leukemia Protein
/ metabolism
Protein Binding
Protein Interaction Mapping
/ methods
Protein Interaction Maps
Protein Processing, Post-Translational
SUMO-1 Protein
/ metabolism
Small Ubiquitin-Related Modifier Proteins
/ metabolism
Sumoylation
Transcription Factors
/ metabolism
Tumor Suppressor Protein p53
/ metabolism
Ubiquitin
/ metabolism
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
18 11 2021
18 11 2021
Historique:
received:
04
01
2021
accepted:
19
10
2021
entrez:
19
11
2021
pubmed:
20
11
2021
medline:
28
12
2021
Statut:
epublish
Résumé
The fast dynamics and reversibility of posttranslational modifications by the ubiquitin family pose significant challenges for research. Here we present SUMO-ID, a technology that merges proximity biotinylation by TurboID and protein-fragment complementation to find SUMO-dependent interactors of proteins of interest. We develop an optimized split-TurboID version and show SUMO interaction-dependent labelling of proteins proximal to PML and RANGAP1. SUMO-dependent interactors of PML are involved in transcription, DNA damage, stress response and SUMO modification and are highly enriched in SUMO Interacting Motifs, but may only represent a subset of the total PML proximal proteome. Likewise, SUMO-ID also allow us to identify interactors of SUMOylated SALL1, a less characterized SUMO substrate. Furthermore, using TP53 as a substrate, we identify SUMO1, SUMO2 and Ubiquitin preferential interactors. Thus, SUMO-ID is a powerful tool that allows to study the consequences of SUMO-dependent interactions, and may further unravel the complexity of the ubiquitin code.
Identifiants
pubmed: 34795231
doi: 10.1038/s41467-021-26807-6
pii: 10.1038/s41467-021-26807-6
pmc: PMC8602451
doi:
Substances chimiques
GTPase-Activating Proteins
0
Promyelocytic Leukemia Protein
0
RANGAP1 protein, human
0
SALL1 protein, human
0
SUMO-1 Protein
0
SUMO1 protein, human
0
SUMO2 protein, human
0
Small Ubiquitin-Related Modifier Proteins
0
Transcription Factors
0
Tumor Suppressor Protein p53
0
Ubiquitin
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
6671Informations de copyright
© 2021. The Author(s).
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