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Properties of highly viscous gels formed by neurofilaments in vitro. A possible consequence of a specific inter-filament cross-bridging.

机译:神经丝在体外形成的高粘度凝胶的特性。特定的细丝间交叉桥接的可能结果。

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摘要

Neurofilaments freshly isolated from bovine spinal cord form a reversible gel in vitro, consisting of nearly parallel and interlinked filaments organized in bundles. This phenomenon is obtained above a critical neurofilament concentration and is highly sensitive to denaturation. No gelation occurs with neurofilaments reconstituted from urea-solubilized subunits. The velocity of the gelation kinetics, optimum at a slightly acidic pH, is inhibited by low and high ionic strength and activated by millimolar concentrations of Mg2+ and other bivalent cations. No protein other than the purified neurofilament preparation itself (80-95% neurofilament triplet) is necessary for the formation of a gel. However, purified cytoskeletal proteins from microtubules and neurofilaments influence the viscosity of the native preparation. These observations suggest a reticulation in vitro between neurofilaments, dependent upon a fragile conformation of the polymers and possibly mediated through the high-Mr neurofilament subunits (200 kDa and 150 kDa). The significance of these results is discussed with regard to the inter-neurofilament cross-bridging in situ involving the 200 kDa subunit described by Hirokawa, Glicksman & Willard [(1984) J. Cell Biol. 98, 1523-1536].
机译:从牛脊髓新鲜分离出的神经丝在体外形成可逆凝胶,由几乎平行且相互连接的丝束组成。该现象在临界神经丝浓度以上获得,并且对变性高度敏感。由尿素溶解的亚基重构的神经丝不会发生凝胶化。低和高离子强度会抑制胶凝动力学的速度(在微酸性pH值下最佳),并且会被毫摩尔浓度的Mg2 +和其他二价阳离子激活。除了纯化的神经丝制备物本身(80-95%的神经丝三联体)以外,不需要蛋白质来形成凝胶。但是,来自微管和神经丝的纯化的细胞骨架蛋白会影响天然制剂的粘度。这些观察结果表明,神经丝之间的网状结构取决于聚合物的脆弱构象,并可能通过高Mr神经丝亚基(200 kDa和150 kDa)介导。关于Hirokawa,Glicksman和Willard [(1984)J.Cell Biol.Natl.Acad.Sci.USA 90:5873-5877]描述的涉及200kDa亚基的神经丝间交叉原位,讨论了这些结果的重要性。 98,1523-1536]。

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