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Substrate identification and specificity profiling of deubiquitylases against endogenously-generated ubiquitin-protein conjugates

ABSTRACT: Deubiquitylating enzymes (DUBs) remove ubiquitin from proteins thereby regulating their stability or activity. Our understanding of DUB-substrate specificity is limited because DUBs are typically not compared to each other against many physiological substrates. By broadly inhibiting DUBs in Xenopus egg extract, we generated hundreds of ubiquitylated proteins and compared the ability of 30 DUBs to deubiquitylate them using quantitative proteomics. We identified five high impact DUBs (USP7, USP9X, USP36, USP15 and USP24) that each reduced ubiquitylation of over ten percent of the isolated proteins. Candidate substrates of high impact DUBs showed substantial overlap and were enriched for disordered regions, suggesting this feature may promote substrate recognition. Other DUBs showed lower impact and non-overlapping specificity, targeting distinct non-disordered proteins including complexes such as the ribosome or the proteasome. Altogether our study identifies candidate DUB substrates and defines patterns of functional redundancy and specificity, revealing substrate characteristics that may influence DUB-substrate recognition.

INSTRUMENT(S): Orbitrap Eclipse, Orbitrap Fusion Lumos

ORGANISM(S): Xenopus Laevis (african Clawed Frog)

SUBMITTER: Joao Paulo

LAB HEAD: Randall W. King

PROVIDER: PXD047866 | Pride | 2024-04-26

REPOSITORIES: Pride

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			Action	DRS
	KeyToRawFiles.xlsx	Xlsx
	a09824.raw	Raw
	a09824_ValX101_Fin2.mzIdentML	Mzid
	a09825.raw	Raw
	a09825_ValX101_Fin2.mzIdentML	Mzid

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