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利用低温电子显微镜对结构动态的核糖体进行成像。

Imaging structurally dynamic ribosomes with cryogenic electron microscopy.

作者信息

Webster Samantha M, May Mira B, Powell Barrett M, Davis Joseph H

出版信息

ArXiv. 2023 Aug 30:arXiv:2308.16019v1.

Abstract

Throughout the history of electron microscopy, ribosomes have served as an ideal subject for imaging and technological development, which in turn has driven our understanding of ribosomal biology. Here, we provide a historical perspective at the intersection of electron microscopy technology development and ribosome biology and reflect on how this technique has shed light on each stage of the life cycle of this dynamic macromolecular machine. With an emphasis on prokaryotic systems, we specifically describe how pairing cryo-EM with clever experimental design, time-resolved techniques, and next-generation heterogeneous structural analysis has afforded insights into the modular nature of assembly, the roles of the many transient biogenesis and translation co-factors, and the subtle variations in structure and function between strains and species. The work concludes with a prospective outlook on the field, highlighting the pivotal role cryogenic electron tomography is playing in adding cellular context to our understanding of ribosomal life cycles, and noting how this exciting technology promises to bridge the gap between cellular and structural biology.

摘要

在电子显微镜的整个历史中,核糖体一直是成像和技术发展的理想研究对象,这反过来又推动了我们对核糖体生物学的理解。在这里,我们从电子显微镜技术发展与核糖体生物学的交叉点提供一个历史视角,并思考这项技术如何揭示了这个动态大分子机器生命周期的每个阶段。我们特别强调原核生物系统,描述了如何将冷冻电镜与巧妙的实验设计、时间分辨技术以及新一代异质结构分析相结合,从而深入了解组装的模块化性质、众多瞬时生物发生和翻译辅助因子的作用,以及不同菌株和物种之间结构和功能的细微差异。这项工作最后对该领域进行了前瞻性展望,强调了低温电子断层扫描在为我们对核糖体生命周期的理解增添细胞背景方面所发挥的关键作用,并指出这项令人兴奋的技术有望弥合细胞生物学与结构生物学之间的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd1/10491319/bed3d5c03fb4/nihpp-2308.16019v1-f0001.jpg

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