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蛋白质运动的原子力显微镜成像:核小体重塑过程中组蛋白H2A-H2B的释放

AFM imaging of protein movements: histone H2A-H2B release during nucleosome remodeling.

作者信息

Bash R, Wang H, Anderson C, Yodh J, Hager G, Lindsay S M, Lohr D

机构信息

Biodesign Institute, Arizona State University, Tempe, AZ 85287-5601, USA.

出版信息

FEBS Lett. 2006 Aug 21;580(19):4757-61. doi: 10.1016/j.febslet.2006.06.101. Epub 2006 Jul 21.

Abstract

Being able to follow assembly/disassembly reactions of biomolecular complexes directly at the single molecule level would be very useful. Here, we use an AFM technique that can simultaneously obtain topographic images and identify the locations of a specific type of protein within those images to monitor the histone H2A component of nucleosomes acted on by human Swi-Snf, an ATP-dependent nucleosome remodeling complex. Activation of remodeling results in significant H2A release from nucleosomes, based on recognition imaging and nucleosome height changes, and changes in the recognition patterns of H2A associated directly with hSwi-Snf complexes.

摘要

能够在单分子水平直接追踪生物分子复合物的组装/拆卸反应将非常有用。在这里,我们使用一种原子力显微镜技术,该技术可以同时获取形貌图像并在这些图像中识别特定类型蛋白质的位置,以监测由人Swi-Snf(一种ATP依赖的核小体重塑复合物)作用的核小体的组蛋白H2A成分。基于识别成像、核小体高度变化以及与hSwi-Snf复合物直接相关的H2A识别模式的变化,重塑的激活导致核小体中大量H2A释放。

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