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The Complete Structure of the Mycobacterium smegmatis 70S Ribosome
Author(s) -
Jendrik Hentschel,
Chloe Burnside,
Ingrid Mignot,
Marc Leibundgut,
Daniel Boehringer,
Nenad Ban
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.06.029
Subject(s) - mycobacterium smegmatis , ribosome , ribosomal rna , mycobacterium tuberculosis , ribosomal protein , computational biology , ribosomal binding site , biology , 5.8s ribosomal rna , translation (biology) , actinobacteria , microbiology and biotechnology , rna , genetics , tuberculosis , bacteria , gene , 16s ribosomal rna , medicine , pathology , messenger rna
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.

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