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

被引:23
作者
Burgoyne, Thomas [1 ]
Morris, Edward P. [2 ]
Luther, Pradeep K. [3 ]
机构
[1] UCL, London WC1E 6BT, England
[2] Inst Canc Res, London SW7 3RP, England
[3] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
关键词
electron tomography; electron microscopy; Z-line; Z-disc; alpha-actinin; ALPHA-ACTININ ROD; SKELETAL-MUSCLE; ELECTRON-MICROSCOPY; CRYSTAL-STRUCTURE; BARBED-END; F-ACTIN; A-BAND; WIDE; RECONSTRUCTION; HETEROGENEITY;
D O I
10.1016/j.jmb.2015.08.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 alpha-actinin, linking antiparallel overlapping ends of the actin filaments from the adjoining sarcomeres. The reconstruction shows that the terminal 5-7 nm of the actin filaments within the Z-band is devoid of any alpha-actinin links and is likely to be the location of capping protein CapZ. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:3527 / 3537
页数:11
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