Abstract
The ubiquitin system regulates virtually all aspects of cellular function. We report a method to target the myriad enzymes that govern ubiquitination of protein substrates. We used massively diverse combinatorial libraries of ubiquitin variants to develop inhibitors of four deubiquitinases (DUBs) and analyzed the DUB-inhibitor complexes with crystallography. We extended the selection strategy to the ubiquitin conjugating (E2) and ubiquitin ligase (E3) enzymes and found that ubiquitin variants can also enhance enzyme activity. Last, we showed that ubiquitin variants can bind selectively to ubiquitin-binding domains. Ubiquitin variants exhibit selective function in cells and thus enable orthogonal modulation of specific enzymatic steps in the ubiquitin system.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Amino Acid Sequence
-
Combinatorial Chemistry Techniques*
-
Conserved Sequence
-
Drug Design
-
Endopeptidases / chemistry
-
Endopeptidases / metabolism*
-
HEK293 Cells
-
Humans
-
Molecular Sequence Data
-
Protease Inhibitors / chemistry
-
Protease Inhibitors / isolation & purification*
-
Protease Inhibitors / pharmacology
-
Protein Conformation
-
Protein Structure, Secondary
-
Small Molecule Libraries
-
Ubiquitin / chemistry
-
Ubiquitin / genetics
-
Ubiquitin / metabolism*
-
Ubiquitin Thiolesterase / chemistry
-
Ubiquitin Thiolesterase / metabolism*
-
Ubiquitin-Conjugating Enzymes / chemistry
-
Ubiquitin-Conjugating Enzymes / metabolism
-
Ubiquitin-Protein Ligases / chemistry
-
Ubiquitin-Protein Ligases / metabolism
-
Ubiquitination / drug effects*
Substances
-
Protease Inhibitors
-
Small Molecule Libraries
-
USP21 protein, human
-
Ubiquitin
-
Ubiquitin-Conjugating Enzymes
-
Ubiquitin-Protein Ligases
-
Endopeptidases
-
Ubiquitin Thiolesterase