| Literature DB >> 33587591 |
Kaitlyn Bacon1, Abigail Blain1, John Bowen1, Matthew Burroughs1, Nikki McArthur1, Stefano Menegatti1,2, Balaji M Rao1,2.
Abstract
Quantifying the binding affinity of protein-protein interactions is important for elucidating connections within biochemical signaling pathways, as well as characterization of binding proteins isolated from combinatorial libraries. We describe a quantitative yeast-yeast two-hybrid (qYY2H) system that not only enables the discovery of specific protein-protein interactions but also efficient, quantitative estimation of their binding affinities (KD). In qYY2H, the bait and prey proteins are expressed as yeast cell surface fusions using yeast surface display. We developed a semiempirical framework for estimating the KD of monovalent bait-prey interactions, using measurements of bait-prey yeast-yeast binding, which is mediated by multivalent interactions between yeast-displayed bait and prey. Using qYY2H, we identified interaction partners of SMAD3 and the tandem WW domains of YAP from a cDNA library and characterized their binding affinities. Finally, we showed that qYY2H could also quantitatively evaluate binding interactions mediated by post-translational modifications on the bait protein.Entities:
Keywords: cDNA library; post-translational modifications; protein engineering; protein−protein interactions; yeast surface display; yeast two-hybrid
Year: 2021 PMID: 33587591 DOI: 10.1021/acssynbio.0c00472
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110