Hisanaga S, Hirokawa N
Department of Anatomy and Cell Biology, School of Medicine, University of Tokyo, Japan.
J Mol Biol. 1988 Jul 20;202(2):297-305. doi: 10.1016/0022-2836(88)90459-7.
The structure of the peripheral domains of neurofilaments (NFs) was revealed by rotary shadowing electron microscopy. NFs were isolated from bovine spinal cords by Sepharose CL-4B gel filtration and examined by low angle rotary shadowing. The peripheral domains appeared as thin, flexible, filamentous structures projecting from the intermediate filament core, with a constant density along their entire length. The average length of the projections was approximately 85 nm and the width about 4 nm. These projections appeared from regularly distributed sites, at 22 nm spacing, which seemed to correspond to the typical repeat of the alpha-helix-rich rod domain of the core filament. The density of the projections was found to be 4.1 (+/- 0.6) per 22 nm. We performed reconstitution experiments using purified NF polypeptides to confirm that the projection was indeed the NF peripheral domain. Individual components of the NF triplet, i.e. NF-L, NF-M and NF-H, were purified by DE-52 and Mono-Q anion exchange chromatographies in the presence of 6 M-urea and were assembled in various combinations into filaments. Reassembled filaments were somewhat more slender than the isolated NFs and exhibited a distinct 22 nm axial periodicity. While prominent projections were not observed in the filaments assembled from NF-L alone, reconstructed filaments containing NF-L plus either NF-M or NF-H revealed many projections. The average length of the projections in the filaments reconstructed from NF-L and NF-H was about 63 nm. The projections of reconstructed filaments from NF-L and NF-M were about 55 nm in length. The difference in the lengths of the projections might reflect the difference in the length of the carboxy-terminal tail domain between NF-M and NF-H. The results are interpreted to show that the carboxy-terminal tail domains of NFs project in a regular pattern from the core filament, which is consistent with a half-staggered organization of the tetrameric subunits.
通过旋转阴影电子显微镜揭示了神经丝(NFs)外周结构域的结构。通过琼脂糖CL-4B凝胶过滤从牛脊髓中分离出NFs,并通过低角度旋转阴影进行检查。外周结构域呈现为从中间丝核心伸出的细的、柔韧的丝状结构,沿其全长密度恒定。突起的平均长度约为85nm,宽度约为4nm。这些突起从规则分布的位点出现,间距为22nm,这似乎对应于核心丝富含α-螺旋的杆状结构域的典型重复。发现突起的密度为每22nm 4.1(±0.6)个。我们使用纯化的NF多肽进行了重组实验,以确认该突起确实是NF外周结构域。NF三联体的各个组分,即NF-L、NF-M和NF-H,在6M尿素存在下通过DE-52和Mono-Q阴离子交换色谱法纯化,并以各种组合组装成丝。重组丝比分离的NFs稍细,并表现出明显的22nm轴向周期性。仅由NF-L组装的丝中未观察到明显的突起,而包含NF-L加NF-M或NF-H的重建丝则显示出许多突起。由NF-L和NF-H重建的丝中突起的平均长度约为63nm。由NF-L和NF-M重建的丝的突起长度约为55nm。突起长度的差异可能反映了NF-M和NF-H之间羧基末端尾结构域长度的差异。结果表明,NFs的羧基末端尾结构域以规则模式从核心丝伸出,这与四聚体亚基的半交错组织一致。