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神经丝的分子结构。I. 中间丝中神经丝L蛋白的亚基排列

Molecular architecture of the neurofilament. I. Subunit arrangement of neurofilament L protein in the intermediate-sized filament.

作者信息

Hisanaga S, Ikai A, Hirokawa N

机构信息

Department of Anatomy and Cell Biology, Faculty of Medicine, University of Tokyo, Japan.

出版信息

J Mol Biol. 1990 Feb 20;211(4):857-69. doi: 10.1016/0022-2836(90)90079-2.

Abstract

Using the smallest subunit (NF-L) of a neurofilament and a glial fibrillary acidic protein, the subunit arrangement in intermediate filaments was studied by low-angle rotary shadowing. NF-L formed a pair of 70 to 80 nm rods in a low ionic strength solution at pH 6.8. Two 70 to 80 nm rods appeared to associate in an antiparallel manner with an overlap of about 55 nm, almost the same length as the alpha-helix-rich central rod domain of intermediate filament proteins. The overlap extended for three-beaded segments, present at 22 nm intervals along the pairs of rods. The observations that (1) 70 to 80 nm rods were a predominant structure in a low ionic strength solution at pH 8.5, (2) the molecular weights of the rod and the pair were measured by sedimentation equilibrium as 190,000 and 37,000 respectively, and (3) the rods formed from the trypsin-digested NF-L had a length of about 47 nm, indicated that the 70 to 80 nm rod is the four-chain complex and the pair of rods is the eight-chain complex. Similar structures were observed with glial fibrillary acidic protein, indicating that these oligomeric structures are common to other intermediate filament proteins. NF-L assembled into short intermediate-sized filaments upon dialysis against a low-salt solution containing 1 to 2 mM-MgCl2 at 4 degrees C. The majority of these short filaments possessed four or five-beaded segments, suggesting that the pair of rods were arranged in a half-staggered fashion in neurofilaments. On the basis of these observations, we propose the following model for the intermediate filament subunit arrangement. (1) The four-chain complex is the 70 to 80 nm rod, in which two coiled-coil molecules align in parallel and in register. (2) Two four-chain complexes form the eight-chain complex by associating in an antiparallel fashion with the overlap of the entire central rod domain. (3) The eight-chain complex is the building block of the intermediate filament. The eight-chain complexes are arranged in a half-staggered fashion within the intermediate filament.

摘要

利用神经丝最小亚基(NF-L)和胶质纤维酸性蛋白,通过低角度旋转阴影法研究了中间丝中的亚基排列。在pH 6.8的低离子强度溶液中,NF-L形成一对70至80纳米的杆状物。两根70至80纳米的杆状物似乎以反平行方式缔合,重叠约55纳米,几乎与中间丝蛋白富含α螺旋的中央杆状结构域长度相同。重叠延伸至三珠节段,沿杆对以22纳米间隔存在。以下观察结果:(1)70至80纳米的杆状物是pH 8.5的低离子强度溶液中的主要结构;(2)通过沉降平衡测得杆状物和双体的分子量分别为190,000和3十七,000;(3)由胰蛋白酶消化的NF-L形成的杆状物长度约为47纳米,表明70至80纳米的杆状物是四链复合物,杆对是八链复合物。用胶质纤维酸性蛋白观察到类似结构,表示这些寡聚结构是其他中间丝蛋白共有的。在4℃下,将NF-L透析到含有1至2 mM MgCl2的低盐溶液中后,其组装成短的中等大小的丝。这些短丝中的大多数具有四或五珠节段,表明杆对在神经丝中以半交错方式排列。基于这些观察结果,我们提出了以下中间丝亚基排列模型。(1)四链复合物是70至80纳米的杆状物,其中两个卷曲螺旋分子平行且对齐排列。(2)两个四链复合物通过以反平行方式缔合,整个中央杆状结构域重叠,形成八链复合物。(3)八链复合物是中间丝的构建块。八链复合物在中间丝内以半交错方式排列。

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