Translation dynamics in human cells visualized at high resolution reveal cancer drug action

• 成果类型: Article
• 署名作者: Xing, Huaipeng; Taniguchi, Reiya; Khusainov, Iskander; Kreysing, Jan Philipp; Welsch, Sonja; Turonova, Beata; Beck, Martin
• 署名单位: Max Planck Society; Goethe University Frankfurt; Max Planck Society; Goethe University Frankfurt
• 刊物名称: SCIENCE
• ISSN/ISSBN: 0036-12930
• DOI: 10.1126/science.adh1411
• 发表日期: 2023-07-07
• 页码: 70-75
• 关键词: ribosome; ORGANIZATION; architecture; tomography; alignment; release

摘要

Ribosomes catalyze protein synthesis by cycling through various functional states. These states have been extensively characterized in vitro, but their distribution in actively translating human cells remains elusive. We used a cryo-electron tomography-based approach and resolved ribosome structures inside human cells with high resolution. These structures revealed the distribution of functional states of the elongation cycle, a Z transfer RNA binding site, and the dynamics of ribosome expansion segments. Ribosome structures from cells treated with Homoharringtonine, a drug used against chronic myeloid leukemia, revealed how translation dynamics were altered in situ and resolve the small molecules within the active site of the ribosome. Thus, structural dynamics and drug effects can be assessed at high resolution within human cells.