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首页> 外文期刊>Journal of Molecular Biology >Muscle Z-band ultrastructure: titin Z-repeats and Z-band periodicities do not match.
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Muscle Z-band ultrastructure: titin Z-repeats and Z-band periodicities do not match.

机译:肌肉Z波段超微结构:Titin Z重复和Z波段周期性不匹配。

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Vertebrate muscle Z-bands show zig-zag densities due to different sets of alpha-actinin cross-links between anti-parallel actin molecules. Their axial extent varies with muscle and fibre type: approximately 50 nm in fast and approximately 100 nm in cardiac and slow muscles, corresponding to the number of alpha-actinin cross-links present. Fish white (fast) muscle Z-bands have two sets of alpha-actinin links, mammalian slow muscle Z-bands have six. The modular structure of the approximately 3 MDa protein titin that spans from M-band to Z-band correlates with the axial structure of the sarcomere; it may form the template for myofibril assembly. The Z-band-located amino-terminal 80 kDa of titin includes 45 residue repeating modules (Z-repeats) that are expressed differentially; heart, slow and fast muscles have seven, four to six and two to four Z-repeats, respectively. Gautel et al. proposed a Z-band model in which each Z-repeat links to one level of alpha-actinin cross-links, requiring that the axial extent of a Z-repeat is the same as the axial separation of alpha-actinin layers, of which there are two in every actin crossover repeat. The span of a Z-repeat in vitro is estimated by Atkinson et al. to be 12 nm or less; much less than half the normal vertebrate muscle actin crossover length of 36 nm. Different actin-binding proteins can change this length; it is reduced markedly by cofilin binding, or can increase to 38.5 nm in the abnormally large nemaline myopathy Z-band. Here, we tested whether in normal vertebrate Z-bands there is a marked reduction in crossover repeat so that it matches twice the apparent Z-repeat length of 12 nm. We found that the measured periodicities in wide Z-bands in slow and cardiac muscles are all very similar, about 39 nm, just like the nemaline myopathy Z-bands. Hence, the 39 nm periodicity is an important conserved feature of Z-bands and either cannot be explained by titin Z-repeats as previously suggested or may correlate with two Z-repeats.
机译:由于反平行肌动蛋白分子之间存在不同组的α-肌动蛋白交联,脊椎动物的肌肉Z带显示出Z字形密度。它们的轴向范围随肌肉和纤维类型的不同而变化:快肌中约50 nm,心肌和慢肌中约100 nm,与存在的α-肌动蛋白交联数相对应。鱼白(快速)肌肉Z波段有两组α-辅肌动蛋白链,哺乳动物慢肌肉Z波段有6条。从M带到Z带的大约3个MDa蛋白纤溶蛋白的模块化结构与肌节的轴向结构相关。它可能形成肌原纤维组装的模板。酪蛋白在Z波段位于氨基末端的80 kDa包含45个差异表达的残基重复模块(Z重复)。心脏,慢和快肌分别有7、4至6和2至4个Z重复。 Gautel等。提出了一种Z带模型,其中每个Z重复序列都链接到一个级别的α-肌动蛋白交联点,要求Z重复的轴向范围与α-肌动蛋白层的轴向间隔相同,其中每个肌动蛋白交叉重复中有两个。 Atkinson等人估计了Z重复体外的跨度。为12nm或更小;远小于正常脊椎动物肌动蛋白交叉长度(36 nm)的一半。不同的肌动蛋白结合蛋白可以改变这个长度。它通过cofilin结合显着降低,或者在异常大的肾上腺肌病Z带中可以增加到38.5 nm。在这里,我们测试了正常脊椎动物Z带中交叉重复是否显着减少,从而使其与表观Z重复长度(12 nm)匹配两倍。我们发现,在慢速和心肌的宽Z波段中,所测量的周期都非常相似,约为39 nm,就像肾上肌肌病Z波段一样。因此,39 nm的周期性是Z波段的一个重要的保守特征,或者不能如先前所建议的那样由titin Z重复来解释,或者可能与两个Z重复相关。

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