Hentschel Jendrik, Burnside Chloe, Mignot Ingrid, Leibundgut Marc, Boehringer Daniel, Ban Nenad
Institute of Molecular Biology and Biophysics, Eidgenössische Technische Hochschule (ETH) Zürich, Otto-Stern-Weg 5, Zürich 8093, Switzerland.
Institute of Molecular Biology and Biophysics, Eidgenössische Technische Hochschule (ETH) Zürich, Otto-Stern-Weg 5, Zürich 8093, Switzerland.
Cell Rep. 2017 Jul 5;20(1):149-160. doi: 10.1016/j.celrep.2017.06.029.
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.
核糖体在每个活细胞中进行蛋白质合成。因此,它是抗菌治疗的一线靶点。结核病是全球主要死因之一,很大程度上是由于难以治疗的潜伏期和抗生素耐药性共同作用的结果。在此,我们展示了耻垢分枝杆菌70S核糖体的3.3埃冷冻电镜结构,耻垢分枝杆菌是人类病原体结核分枝杆菌的近亲。该结构揭示了另外两种核糖体蛋白,并将它们定位在核糖体催化中心和解码位点的药物靶点附近。此外,我们可视化了放线菌特有的rRNA和蛋白质扩展,这些扩展广泛重塑了核糖体表面,对多核糖体组织有影响。我们的结果为理解分枝杆菌翻译的特性提供了基础,并揭示了该结构的原子细节,这将有助于抗结核治疗药物的设计。