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冷冻电镜:分辨率革命与药物发现。

Cryo-EM: The Resolution Revolution and Drug Discovery.

机构信息

Structure, Biophysics and FBLG, Discovery Sciences, AstraZeneca R&D, Cambridge, UK.

出版信息

SLAS Discov. 2021 Jan;26(1):17-31. doi: 10.1177/2472555220960401. Epub 2020 Oct 5.

Abstract

Single-particle cryogenic electron microscopy (cryo-EM) has been elevated to the mainstream of structural biology propelled by technological advancements in numerous fronts, including imaging analysis and the development of direct electron detectors. The drug discovery field has watched with (initial) skepticism and wonder at the progression of the technique and how it revolutionized the molecular understanding of previously intractable targets. This article critically assesses how cryo-EM has impacted drug discovery in diverse therapeutic areas. Targets that have been brought into the realm of structure-based drug design by cryo-EM and are thus reviewed here include membrane proteins like the GABA receptor, several TRP channels, and G protein-coupled receptors, and multiprotein complexes like the ribosomes, the proteasome, and eIF2B. We will describe these studies highlighting the achievements, challenges, and caveats.

摘要

单颗粒低温电子显微镜(cryo-EM)在多个领域的技术进步的推动下,已经上升到结构生物学的主流,包括成像分析和直接电子探测器的发展。药物发现领域一直在(最初)怀疑和惊叹于该技术的进展,以及它如何彻底改变了以前难以捉摸的靶点的分子理解。本文批判性地评估了 cryo-EM 如何在不同的治疗领域影响药物发现。通过 cryo-EM 进入基于结构的药物设计领域的靶点包括 GABA 受体等膜蛋白、几种 TRP 通道和 G 蛋白偶联受体,以及核糖体、蛋白酶体和 eIF2B 等多蛋白复合物。我们将描述这些研究,突出其成就、挑战和注意事项。

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