Visualizing flexibility at molecular resolution: analysis of heterogeneity in single-particle electron microscopy reconstructions.

Andres E Leschziner, Eva Nogales
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引用次数: 108

Abstract

It is becoming increasingly clear that many macromolecules are intrinsically flexible and exist in multiple conformations in solution. Single-particle reconstruction of vitrified samples (cryo-electron microscopy, or cryo-EM) is uniquely positioned to visualize this conformational flexibility in its native state. Although heterogeneity remains a significant challenge in cryo-EM single-particle analysis, recent efforts in the field point to a future where it will be possible to tap into this rich source of biological information on a routine basis. In this article, we review the basic principles behind a few relatively new and generally applicable methods that show particular promise as tools to analyze macromolecular flexibility. We also discuss some of their recent applications to problems of biological interest.

可视化柔韧性在分子分辨率:分析异质性在单粒子电子显微镜重建。
越来越清楚的是,许多大分子本质上是柔性的,并且在溶液中以多种构象存在。玻璃化样品的单粒子重建(低温电子显微镜,或低温电子显微镜)是独特的定位,以可视化这种构象的灵活性在其原生状态。尽管在低温电镜单粒子分析中,异质性仍然是一个重大挑战,但最近在该领域的努力表明,未来将有可能在常规基础上挖掘这一丰富的生物信息来源。在本文中,我们回顾了一些相对较新的和普遍适用的方法背后的基本原理,这些方法显示出特别有希望作为分析大分子灵活性的工具。我们还讨论了它们最近在生物学问题上的一些应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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