Engineering of ultraID, a compact and hyperactive enzyme for proximity-dependent biotinylation in living cells.

ABSTRACT: Proximity-dependent biotinylation (PDB) combined with mass spectrometry analysis has established itself as a key technology to study protein-protein interactions in living cells. A widespread approach, BioID, uses an abortive variant of the E. coli BirA biotin protein ligase, a quite bulky enzyme with slow labeling kinetics. To improve PDB versatility and speed, various enzymes have been developed by different approaches. Here we present a small-size engineered enzyme: ultraID. We show its practical use to probe the interactome of Argonaute-2 after a 10 min labeling pulse and expression at physiological levels. Moreover, using ultraID, we provide a membrane-associated interactome of coatomer, the coat protein complex of COPI vesicles. To date, ultraID is the smallest and most efficient bio

SUBMITTER: Kubitz L 

PROVIDER: S-EPMC9253107 | biostudies-literature | 2022 Jul

REPOSITORIES: biostudies-literature