Our understanding of protein synthesis has been conceptualised around the structure and function of the bacterial ribosome. This complex macromolecular machine is the target of important antimicrobial drugs, an integral line of defence against infectious diseases. Here, we describe how open access to cryo-electron microscopy facilities combined with bespoke user support enabled structural determination of the translating ribosome from Escherichia coli at 1.55âà resolution. The obtained structures allow for direct determination of the rRNA sequence to identify ribosome polymorphism sites in the E. coli strain used in this study and enable interpretation of the ribosomal active and peripheral sites at unprecedented resolution. This includes scarcely populated chimeric hybrid states of the ribosome engaged in several tRNA translocation steps resolved at ~2âà resolution. The current map not only improves our understanding of protein synthesis but also allows for more precise structure-based drug design of antibiotics to tackle rising bacterial resistance.
The translating bacterial ribosome at 1.55âà resolution generated by cryo-EM imaging services.
利用冷冻电镜成像服务生成的分辨率为 1.55° 的翻译细菌核糖体图像
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作者:Fromm Simon A, O'Connor Kate M, Purdy Michael, Bhatt Pramod R, Loughran Gary, Atkins John F, Jomaa Ahmad, Mattei Simone
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2023 | 起止号: | 2023 Feb 25; 14(1):1095 |
| doi: | 10.1038/s41467-023-36742-3 | 研究方向: | 微生物学 |
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