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脊椎动物肌肉Z线的三维结构:大鼠心肌中的小方格晶格Z线

Three-Dimensional Structure of Vertebrate Muscle Z-Band: The Small-Square Lattice Z-Band in Rat Cardiac Muscle.

作者信息

Burgoyne Thomas, Morris Edward P, Luther Pradeep K

机构信息

University College London, London WC1E 6BT, United Kingdom.

Institute of Cancer Research, London SW7 3RP, United Kingdom.

出版信息

J Mol Biol. 2015 Nov 6;427(22):3527-3537. doi: 10.1016/j.jmb.2015.08.018. Epub 2015 Sep 8.

DOI:10.1016/j.jmb.2015.08.018
PMID:26362007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4641244/
Abstract

The Z-band in vertebrate striated muscle crosslinks actin filaments of opposite polarity from adjoining sarcomeres and transmits tension along myofibrils during muscular contraction. It is also the location of a number of proteins involved in signalling and myofibrillogenesis; mutations in these proteins lead to myopathies. Understanding the high-resolution structure of the Z-band will help us understand its role in muscle contraction and the role of these proteins in the function of muscle. The appearance of the Z-band in transverse-section electron micrographs typically resembles a small-square lattice or a basketweave appearance. In longitudinal sections, the Z-band width varies more with muscle type than species: slow skeletal and cardiac muscles have wider Z-bands than fast skeletal muscles. As the Z-band is periodic, Fourier methods have previously been used for three-dimensional structural analysis. To cope with variations in the periodic structure of the Z-band, we have used subtomogram averaging of tomograms of rat cardiac muscle in which subtomograms are extracted and compared and similar ones are averaged. We show that the Z-band comprises four to six layers of links, presumably α-actinin, linking antiparallel overlapping ends of the actin filaments from the adjoining sarcomeres. The reconstruction shows that the terminal 5-7nm of the actin filaments within the Z-band is devoid of any α-actinin links and is likely to be the location of capping protein CapZ.

摘要

脊椎动物横纹肌中的Z线连接相邻肌节中极性相反的肌动蛋白丝,并在肌肉收缩过程中沿肌原纤维传递张力。它也是许多参与信号传导和肌原纤维生成的蛋白质的所在位置;这些蛋白质的突变会导致肌病。了解Z线的高分辨率结构将有助于我们理解其在肌肉收缩中的作用以及这些蛋白质在肌肉功能中的作用。在横断面电子显微镜照片中,Z线的外观通常类似于小方格晶格或篮状编织外观。在纵切面中,Z线的宽度随肌肉类型的变化比随物种的变化更大:慢肌骨骼肌和心肌的Z线比快肌骨骼肌的Z线更宽。由于Z线是周期性的,傅里叶方法以前曾用于三维结构分析。为了应对Z线周期性结构的变化,我们对大鼠心肌的断层扫描图像进行了亚断层平均,其中提取并比较了亚断层图像,并对相似的图像进行了平均。我们发现,Z线由四到六层连接组成,推测为α-辅肌动蛋白,连接相邻肌节中肌动蛋白丝的反平行重叠末端。重建结果表明,Z线内肌动蛋白丝末端5-7纳米没有任何α-辅肌动蛋白连接,可能是封端蛋白CapZ的所在位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/f6334c2f0fc1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/7c8003d8b490/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/e001370ca30d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/28c352f8f50a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/e6163e8b139e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/f6334c2f0fc1/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/7c8003d8b490/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/e001370ca30d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/28c352f8f50a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/e6163e8b139e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72a5/4641244/f6334c2f0fc1/gr4.jpg

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The structure and regulation of human muscle α-actinin.人类肌肉α-辅肌动蛋白的结构与调控
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