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由肌肉细胞和成纤维细胞的中间丝亚基进行同聚物和共聚物细丝的体外组装。

In vitro assembly of homopolymer and copolymer filaments from intermediate filament subunits of muscle and fibroblastic cells.

作者信息

Steinert P M, Idler W W, Cabral F, Gottesman M M, Goldman R D

出版信息

Proc Natl Acad Sci U S A. 1981 Jun;78(6):3692-6. doi: 10.1073/pnas.78.6.3692.

Abstract

This paper presents evidence that the intermediate filament (IF) subunits of muscle cells (skeletin or desmin) and fibroblastic cells (decamin or vimentin) separately form homopolymer IF in vitro and, when mixed, prefer to form copolymer IF in vitro. Because they coexist in cells, they may also form copolymers in vivo. The IFs of baby hamster kidney fibroblasts (BHK-21) consist of a major subunit, decamin, and two minor subunits which, on the basis of two-dimensional gel and peptide mapping criteria, are identical to the alpha and beta subunits of smooth muscle desmin. The subunits differ only in their degrees of phosphorylation: alpha desmin contained 2 mol/mol of O-phosphoserine whereas beta desmin contained none. The decamin and desmin subunits assembled into homopolymer IF in vitro in high yield from purified denatured subunits under identical conditions of pH and ionic strength. However, homopolymer decamin IF disassembled into soluble protofilaments in solutions of ionic strength less than 0.05 mol/liter whereas homopolymer desmin IF disassembled at ionic strength less than 0.03 mol/liter. When decamin and desmin were mixed together as denatured subunits or as soluble protofilaments, the IF assembled in vitro had solubility properties intermediate between those of the homopolymer IFs, indicating that the two subunits had formed copolymer IF. The stoichiometry of copolymerization as determined in mixtures in which one subunit was present in excess was suggestive of the formation of three-chain units. The possibility of nonspecific aggregation was eliminated by isolation of stable three-chain alpha-helix-enriched particles from such IF. When tracer amounts of [35S]methionine-labeled decamin were mixed with desmin, labeled IFs were obtained under conditions in which homopolymer decamin IFs were soluble. These in vitro findings may be of physiological significance because native BHK-21 IF also had solubility properties similar to those of the copolymer IF.

摘要

本文提供的证据表明,肌肉细胞的中间丝(IF)亚基(肌纤蛋白或结蛋白)和成纤维细胞的中间丝亚基(十聚蛋白或波形蛋白)在体外分别形成同聚物IF,并且在混合时,更倾向于在体外形成共聚物IF。由于它们在细胞中共存,因此在体内也可能形成共聚物。幼仓鼠肾成纤维细胞(BHK-21)的IF由一个主要亚基十聚蛋白和两个次要亚基组成,根据二维凝胶和肽图谱标准,这两个次要亚基与平滑肌结蛋白的α和β亚基相同。这些亚基仅在磷酸化程度上有所不同:α结蛋白含有2摩尔/摩尔的O-磷酸丝氨酸,而β结蛋白则不含。在相同的pH和离子强度条件下,十聚蛋白和结蛋白亚基从纯化的变性亚基中以高产率在体外组装成同聚物IF。然而,同聚物十聚蛋白IF在离子强度小于0.05摩尔/升的溶液中解聚成可溶性原丝,而同聚物结蛋白IF在离子强度小于0.03摩尔/升时解聚。当十聚蛋白和结蛋白作为变性亚基或可溶性原丝混合在一起时,体外组装的IF具有介于同聚物IF之间的溶解性,表明这两个亚基形成了共聚物IF。在一种亚基过量的混合物中测定的共聚化学计量比表明形成了三链单元。通过从这种IF中分离出稳定的富含三链α-螺旋的颗粒,排除了非特异性聚集的可能性。当将微量的[35S]甲硫氨酸标记的十聚蛋白与结蛋白混合时,在同聚物十聚蛋白IF可溶的条件下获得了标记的IF。这些体外研究结果可能具有生理学意义,因为天然的BHK-21 IF也具有与共聚物IF相似的溶解性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab6d/319637/5fffe4192fc6/pnas00657-0431-a.jpg

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