| Literature DB >> 34353925 |
Marion Thépaut1,2, Rodrigo Campos-Silva1,3, Eva Renard4, Frédérique Barloy-Hubler1, Eric Ennifar4, Daniel Boujard1, Reynald Gillet1.
Abstract
In bacteria, trans-translation is the major quality control system for rescuing stalled ribosomes. It is mediated by tmRNA, a hybrid RNA with properties of both a tRNA and a mRNA, and the small protein SmpB. Because trans-translation is absent in eukaryotes but necessary for bacterial fitness or survival, it is a promising target for the development of novel antibiotics. To facilitate screening of chemical libraries, various reliable in vitro and in vivo systems have been created for assessing trans-translational activity. However, the aim of the current work was to permit the safe and easy in vitro evaluation of trans-translation from pathogenic bacteria, which are obviously the ones we should be targeting. Based on green fluorescent protein (GFP) reassembly during active trans-translation, we have created a cell-free assay adapted to the rapid evaluation of trans-translation in ESKAPE bacteria, with 24 different possible combinations. It can be used for easy high-throughput screening of chemical compounds as well as for exploring the mechanism of trans-translation in these pathogens.Entities:
Keywords: ESKAPE; HTS; antibiotics; ribosome; tmRNA; trans-translation
Mesh:
Substances:
Year: 2021 PMID: 34353925 PMCID: PMC8522692 DOI: 10.1261/rna.078773.121
Source DB: PubMed Journal: RNA ISSN: 1355-8382 Impact factor: 4.942