| Literature DB >> 28683309 |
Jendrik Hentschel1, Chloe Burnside1, Ingrid Mignot1, Marc Leibundgut1, Daniel Boehringer1, Nenad Ban2.
Abstract
The ribosome carries out the synthesis of proteins in every living cell. It consequently represents a frontline target in anti-microbial therapy. Tuberculosis ranks among the leading causes of death worldwide, due in large part to the combination of difficult-to-treat latency and antibiotic resistance. Here, we present the 3.3-Å cryo-EM structure of the 70S ribosome of Mycobacterium smegmatis, a close relative to the human pathogen Mycobacterium tuberculosis. The structure reveals two additional ribosomal proteins and localizes them to the vicinity of drug-target sites in both the catalytic center and the decoding site of the ribosome. Furthermore, we visualized actinobacterium-specific rRNA and protein expansions that extensively remodel the ribosomal surface with implications for polysome organization. Our results provide a foundation for understanding the idiosyncrasies of mycobacterial translation and reveal atomic details of the structure that will facilitate the design of anti-tubercular therapeutics.Entities:
Keywords: Actinobacterium; Mycobacterium; antibiotic; cryo-EM; polysome; ribosome; translation
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Year: 2017 PMID: 28683309 DOI: 10.1016/j.celrep.2017.06.029
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423