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一种新颖的方法用于分析部分修饰的肌动蛋白丝的结构。

A novel approach to the structural analysis of partially decorated actin based filaments.

机构信息

Institute of Cancer Research, Chester Beatty Laboratories, 237, Fulham Road, London SW3 6JB, UK.

出版信息

J Struct Biol. 2010 May;170(2):278-85. doi: 10.1016/j.jsb.2009.12.010. Epub 2009 Dec 16.

Abstract

We describe a novel set of single particle based procedures for the structural analysis of electron microscope images of muscle thin filaments and other partially decorated actin based filaments. The thin filament comprises actin and the regulatory proteins tropomyosin and troponin in a 7:1:1M ratio. Prior to our work, structure analysis from electron microscope images of the thin filament has largely involved either helical averaging defined by the underlying actin helix or the use of single particle analysis but using a starting model as a reference structure. Our single particle based approach yields an accurate structure for the complete thin filament by avoiding the loss of information from troponin and tropomyosin associated with helical averaging and also removing the potential reference bias associated with the use of a starting model. The approach is more widely applicable to sub-stoichiometric complexes of F-actin and actin-binding proteins.

摘要

我们描述了一套新的基于单颗粒的程序,用于分析肌肉细丝和其他部分修饰的肌动蛋白丝的电子显微镜图像的结构。细丝由肌动蛋白和调节蛋白原肌球蛋白和肌钙蛋白以 7:1:1M 的比例组成。在我们的工作之前,来自细丝电子显微镜图像的结构分析在很大程度上涉及到由基础肌动蛋白螺旋定义的螺旋平均化,或者使用单颗粒分析,但使用起始模型作为参考结构。我们的基于单颗粒的方法通过避免与螺旋平均化相关的肌钙蛋白和原肌球蛋白的信息丢失,以及消除使用起始模型相关的潜在参考偏差,从而为完整的细丝产生准确的结构。该方法更广泛地适用于肌动蛋白和肌动蛋白结合蛋白的亚化学计量复合物。

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