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鱿鱼巨轴突中的轴突下细胞骨架。I. 微管、微丝及其相关高分子量蛋白质的生化分析。

Subaxolemmal cytoskeleton in squid giant axon. I. Biochemical analysis of microtubules, microfilaments, and their associated high-molecular-weight proteins.

作者信息

Kobayashi T, Tsukita S, Tsukita S, Yamamoto Y, Matsumoto G

出版信息

J Cell Biol. 1986 May;102(5):1699-709. doi: 10.1083/jcb.102.5.1699.

Abstract

Using the squid giant axon, we analyzed biochemically the molecular organization of the axonal cytoskeleton underlying the axolemma (subaxolemmal cytoskeleton). The preparation enriched in the subaxolemmal cytoskeleton was obtained by squeezing out the central part of the axoplasm using a roller. The electrophoretic banding pattern of the subaxolemmal cytoskeleton was characterized by large amounts of two high-molecular-weight (HMW) proteins (260 and 255 kD). The alpha, beta-tubulin, actin, and some other proteins were also its major constituents. The 260-kD protein is known to play an important role in maintaining the excitability of the axolemma (Matsumoto, G., M. Ichikawa, A. Tasaki, H. Murofushi, and H. Sakai, 1983, J. Membr. Biol., 77:77-91) and was recently designated "axolinin" (Sakai, H., G. Matsumoto, and H. Murofushi, 1985, Adv. Biophys., 19:43-89). We purified axolinin and the 255-kD protein in their native forms and further characterized their biochemical properties. The purified axolinin was soluble in 0.6 M NaCl solution but insoluble in 0.1 M NaCl solution. It co-sedimented with microtubules but not with actin filaments. In low-angle rotary-shadowing electron microscopy, the axolinin molecule in 0.6 M NaCl solution looked like a straight rod approximately 105 nm in length with a globular head at one end. On the other hand, the purified 255-kD protein was soluble in both 0.1 and 0.6 M NaCl solution and co-sedimented with actin filaments but not with microtubules. The 255-kD protein molecule appeared as a characteristic horseshoe-shaped structure approximately 35 nm in diameter. Furthermore, the 255-kD protein showed no cross-reactivity to the anti-axolinin antibody. Taken together, these characteristics lead us to conclude that the subaxolemmal cytoskeleton in the squid giant axon is highly specialized, and is mainly composed of microtubules and a microtubule-associated HMW protein (axolinin), and actin filaments and an actin filament-associated HMW protein (255-kD protein).

摘要

我们利用枪乌贼巨大轴突,对轴膜下(轴膜下细胞骨架)轴突细胞骨架的分子组织进行了生化分析。通过用滚筒挤出轴浆的中央部分,获得了富含轴膜下细胞骨架的制剂。轴膜下细胞骨架的电泳条带模式的特征是含有大量两种高分子量(HMW)蛋白质(260和255kD)。α、β微管蛋白、肌动蛋白和其他一些蛋白质也是其主要成分。已知260-kD蛋白质在维持轴膜的兴奋性方面起重要作用(松本,G.,市川,M.,田崎,A.,室伏,H.,和酒井,H.,1983,《膜生物学杂志》,77:77-91),最近被命名为“轴突素”(酒井,H.,松本,G.,和室伏,H.,1985,《生物物理学进展》,19:43-89)。我们以天然形式纯化了轴突素和255-kD蛋白质,并进一步表征了它们的生化特性。纯化的轴突素可溶于0.6M NaCl溶液,但不溶于0.1M NaCl溶液。它与微管共同沉降,但不与肌动蛋白丝共同沉降。在低角度旋转阴影电子显微镜下,0.6M NaCl溶液中的轴突素分子看起来像一根长约105nm的直杆,一端有一个球状头部。另一方面,纯化的255-kD蛋白质可溶于0.1M和0.6M NaCl溶液,并与肌动蛋白丝共同沉降,但不与微管共同沉降。255-kD蛋白质分子呈现出直径约35nm的特征性马蹄形结构。此外,255-kD蛋白质与抗轴突素抗体没有交叉反应。综上所述,这些特征使我们得出结论,枪乌贼巨大轴突中的轴膜下细胞骨架高度特化,主要由微管和一种与微管相关的高分子量蛋白质(轴突素),以及肌动蛋白丝和一种与肌动蛋白丝相关的高分子量蛋白质(255-kD蛋白质)组成。

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