Author: Yang, X.; Lennard, K.R.; He, C.; Walker, M.C.; Ball, A.T.; Doigneaux, C.; Tavassoli, A.; van der Donk, W.A.
Description: In this article we describe the production and screening of a genetically encoded library of 10(6) lanthipeptides in Escherichia coli using the substrate-tolerant lanthipeptide synthetase ProcM. This plasmid-encoded library was combined with a bacterial reverse two-hybrid system for the interaction of the HIV p6 protein with the UEV domain of the human TSG101 protein, which is a critical protein-protein interaction for HIV budding from infected cells. Using this approach, we identified an inhibitor of this interaction from the lanthipeptide library, whose activity was verified in vitro and in cell-based virus-like particle-budding assays. Given the variety of lanthipeptide backbone scaffolds that may be produced with ProcM, this method may be used for the generation of genetically encoded libraries of natural product-like lanthipeptides containing substantial structural diversity. Such libraries may be combined with any cell-based assay to identify lanthipeptides with new biological activities.
Subject Headings: Lanthipeptide; Protein; Inhibitor
Subject headings:
Publication year: 2018
Journal or book title: Nature Chemical Biology
Volume: 14
Issue: 4
Pages: 375-380
Find the full text : https://www.nature.com/articles/s41589-018-0008-5
Find more like this one (cited by): https://scholar.google.com/scholar?cites=12654640343126388252&as_sdt=1000005&sciodt=0,16&hl=en
Type: Journal Article
Serial number: 2272