首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Molecular organization of C9 within the membrane attack complex of complement. Induction of circular C9 polymerization by the C5b-8 assembly
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Molecular organization of C9 within the membrane attack complex of complement. Induction of circular C9 polymerization by the C5b-8 assembly

机译:膜攻击复合物内的C9分子组织。通过C5b-8组件诱导循环C9聚合

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摘要

Evidence has been presented suggesting that during assembly of the membrane attack complex (MAC) of complement, the C5b-8 complex induces polymerization of C9. The C9 polymer was detected by sodium dodecyl sulfate (SDS) gel electrophoresis of MAC isolated from complement-lysed erythrocytes. It resembled the previously described polymerized C9 (poly C9) produced from isolated monomeric C9 by prolonged incubation at 37 degrees C in that it was resistant to dissociation by SDS and reducing agents and had an apparent molecular weight of approximately 1.1 million. The presence of poly C9 in the MAC was further supported by the expression of identical neoantigens by the MAC and poly C9 and by the high C9 content of the MAC relative to its other constituents. Isolated C8 in solution was found to have a single C9-binding site. In mixture, the two proteins formed a reversible equimolar complex that had a sedimentation coefficient of 10.5S. In contrast, a single, cell-bound C5b-8 complex was found to bind up to 12-15 C9 molecules and clusters of C5b- 8 bound 6-8 C9 molecules per C8 molecule. In either case, typical ultrastructural membrane lesions were observed, suggesting that the membrane lesion is identical with the tubular poly C9 consisting of 12-16 C9 molecules, and that the MAC can have either the composition (C5b-8)polyC9 or (CSb-8)(2)polyC9. When C9 input was restricted so that the molar C9/C8 ratio was less than or equal to 3, C9-induced aggregates of C5b-8 were observed but virtually no circular membrane lesions were found. We suggest, therefore, that C9, at low dosage, causes cross-linking of multiple C5b-8 complexes within the target membrane and that, at high dosage, C9 is polymerized by C5b-8 to form a transmembrane channel within the MAC assembly. It is primarily the C9 polymer that evokes the ultrastructural image of the MAC or of membrane lesions caused by complement.
机译:已有证据表明,在补体的膜攻击复合物(MAC)组装过程中,C5b-8复合物诱导C9聚合。通过从补体溶解的红细胞分离的MAC的十二烷基硫酸钠(SDS)凝胶电泳检测C9聚合物。它类似于先前描述的通过在37°C下长时间孵育而由分离的单体C9制备的聚合C9(聚C9),因为它对SDS和还原剂具有抗解离性,并且具有约110万的表观分子量。 MAC和poly C9表达相同的新抗原,并且相对于其其他成分,MAC的高C9含量进一步支持了MAC中poly C9的存在。发现溶液中分离的C8具有单个C9结合位点。两种蛋白质混合形成可逆的等摩尔复合物,其沉降系数为10.5S。相反,发现单个细胞结合的C5b-8复合物最多结合12-15个C9分子,并且每个C8分子结合C5b-8结合的簇6-8个C9分子。在这两种情况下,均观察到典型的超微结构膜病变,表明该膜病变与由12-16个C9分子组成的管状聚C9相同,并且MAC可以具有(C5b-8)polyC9或(CSb- 8)(2)polyC9。当限制C9输入以使C9 / C8摩尔比小于或等于3时,观察到C9诱导的C5b-8聚集体,但实际上未发现圆形膜损伤。因此,我们建议低剂量的C9引起靶膜内多个C5b-8络合物的交联,高剂量的C9被C5b-8聚合形成MAC组件内的跨膜通道。主要是C9聚合物引起MAC或补体引起的膜病变的超微结构图像。

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