Sharkey, LKR and O'Neill, AJ orcid.org/0000-0003-3222-5493 (2018) Antibiotic Resistance ABC-F Proteins: Bringing Target Protection into the Limelight. ACS Infectious Diseases, 4 (3). pp. 239-246. ISSN 2373-8227
Abstract
Members of the ATP-binding cassette (ABC)-F protein subfamily collectively mediate resistance to a broader range of clinically important antibiotic classes than any other group of resistance proteins and are widespread in pathogenic bacteria. Following over 25 years’ of controversy regarding the mechanism by which these proteins work, it has recently been established that they provide antibiotic resistance through the previously recognized but underappreciated phenomenon of target protection; they bind to the ribosome to effect the release of ribosome-targeted antibiotics, thereby rescuing the translation apparatus from antibiotic-mediated inhibition. Here we review the ABC-F resistance proteins with an emphasis on their mechanism of action, first exploring the history of the debate about how these proteins work and outlining our current state of knowledge and then considering key questions to be addressed in understanding the molecular detail of their function.
Metadata
Item Type: | Article |
---|---|
Authors/Creators: |
|
Copyright, Publisher and Additional Information: | (c) 2018, American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Infectious Diseases, copyright (c) American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see: https://doi.org/10.1021/acsinfecdis.7b00251 |
Keywords: | ABC proteins; lsa(A); msr(A); msr(D); optrA; protein synthesis inhibitors; vga(A) |
Dates: |
|
Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) > Molecular Microbiology (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 09 Feb 2018 14:25 |
Last Modified: | 27 Jan 2019 01:38 |
Status: | Published |
Publisher: | American Chemical Society |
Identification Number: | 10.1021/acsinfecdis.7b00251 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:127132 |