Split ubiquitin as a sensor of protein interactions in vivo.

• DOI: 10.1073/pnas.91.22.10340
• Publication Date: 2006-05-31T12:58:56Z
• Authors: N Johnsson; A Varshavsky
• Keywords: 0301 basic medicine; 570; Protein Folding; Protein Conformation; Recombinant Fusion Proteins; Saccharomyces cerevisiae; GENE ENCODES; Protein Structure, Secondary; SACCHAROMYCES-CEREVISIAE; Mice; 03 medical and health sciences; Animals; YEAST; PROTEOLYSIS; Ubiquitins; LEUCINE ZIPPER; IDENTIFICATION; POLYPEPTIDES; DNA; Peptide Fragments; FAMILY; Models, Structural; Tetrahydrofolate Dehydrogenase; SYSTEM; Caltech Library Services; Biomarkers

We describe an assay for in vivo protein interactions. Protein fusions containing ubiquitin, a 76-residue, single-domain protein, are rapidly cleaved in vivo by ubiquitin-specific proteases, which recognize the folded conformation of ubiquitin. When a C-terminal fragment of ubiquitin (C(ub)) is expressed as a fusion to a reporter protein, the fusion is cleaved only if an N-terminal fragment of ubiquitin (Nub) is also expressed in the same cell. This reconstitution of native ubiquitin from its fragments, detectable by the in vivo cleavage assay, is not observed with a mutationally altered Nub. However, if C(ub) and the altered Nub are each linked to polypeptides that interact in vivo, the cleavage of the fusion containing C(ub) is restored, yielding a generally applicable assay for kinetic and equilibrium aspects of in vivo protein interactions. This method, termed USPS (ubiquitin-based split-protein sensor), makes it possible to monitor a protein-protein interaction as a function of time, at the natural sites of this interaction in a living cell.