| Literature DB >> 34821011 |
David M Boragine1, Wanzhi Huang2, Lynn H Su2, Timothy Palzkill2.
Abstract
Disrupting protein-protein interactions is difficult due to the large and flat interaction surfaces of the binding partners. The BLIP and BLIP-II proteins are unrelated in sequence and structure and yet each potently inhibit β-lactamases. High-throughput oligonucleotide synthesis was used to construct a 12,470-member library containing overlapping linear and cyclic peptides ranging in size from 6 to 21 amino acids that scan through the sequences of BLIP and BLIP-II. Phage display affinity selections and deep sequencing revealed that, despite the differences in interaction surfaces with β-lactamases, rapid enrichment of consensus peptide regions originating from both BLIP and BLIP-II contact residues in the binding interface occurred. BLIP and BLIP-II peptides that were enriched by affinity selection were shown to bind β-lactamases and disrupt the BLIP/β-lactamase interaction. The results suggest that peptides that bind at and disrupt PPI interfaces can be identified through systematic peptide library construction, affinity selection, and deep sequencing.Entities:
Keywords: bioinformatics; peptide libraries; peptides; phage display; protein-protein interactions
Mesh:
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Year: 2021 PMID: 34821011 PMCID: PMC8939392 DOI: 10.1002/cbic.202100504
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164