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补体第九成分(C9)的聚合:形成具有类似于补体膜攻击复合物的管状超微结构的多聚(C9)。

Polymerization of the ninth component of complement (C9): formation of poly(C9) with a tubular ultrastructure resembling the membrane attack complex of complement.

作者信息

Podack E R, Tschopp J

出版信息

Proc Natl Acad Sci U S A. 1982 Jan;79(2):574-8. doi: 10.1073/pnas.79.2.574.

DOI:10.1073/pnas.79.2.574
PMID:6952208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC345787/
Abstract

The ninth component of complement (C9) has a marked propensity to polymerize. C9 polymers [poly(C9)] formed spontaneously in Veronal-buffered saline upon incubation of purified C9 for 64 hr at 37 degrees C or within 2 hr at 46--56 degrees C. Poly(C9) formed at 37 degrees C was visualized by electron microscopy as a tubular structure with an internal diameter of 110 A and a length of 160 A. Its ultrastructure suggested a dodecameric composition and resembled that of the membrane attack complex of complement. The wider end of the tubular structure was formed by an approximately 30-A-thick torus with inner and outer diameters of 110 A and 220 A, respectively. Because the dimensions of C9 within poly(C9) were 160 x 55 A (maximal) and 20 A (minimal) and because monomeric C9 has dimensions of approximately 80 x 55 A, it is proposed that monomeric C9 unfolds during polymerization into tubules. Polymerization also occurred upon treatment of C9 for 1 hr at 37 degrees C with 0.6 M guanidine . HCl, 0.1 M octyl glucoside, or 1.5% sodium deoxycholate. Guanidine . HCl-induced C9 polymers consisted of elongated highly curved strands 55--80 A wide, suggesting that these polymers were formed by globular C9 that had not unfolded.

摘要

补体第九成分(C9)具有显著的聚合倾向。纯化的C9在37℃下于巴比妥缓冲盐溶液中孵育64小时或在46 - 56℃下2小时内会自发形成C9聚合物[聚(C9)]。在37℃形成的聚(C9)通过电子显微镜观察为管状结构,其内径为110埃,长度为160埃。其超微结构表明为十二聚体组成,类似于补体的膜攻击复合物。管状结构较宽的一端由一个约30埃厚的环面形成,其内径和外径分别为110埃和220埃。由于聚(C9)内C9的尺寸为160×55埃(最大)和20埃(最小),且单体C9的尺寸约为80×55埃,因此有人提出单体C9在聚合成小管的过程中会展开。用0.6M盐酸胍、0.1M辛基葡糖苷或1.5%脱氧胆酸钠在37℃处理C9 1小时也会发生聚合。盐酸胍诱导的C9聚合物由宽55 - 80埃的细长高度弯曲链组成,这表明这些聚合物是由未展开的球状C9形成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cee1/345787/97e0c1a4bda8/pnas00441-0376-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cee1/345787/f65bb0e03fa3/pnas00441-0375-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cee1/345787/97e0c1a4bda8/pnas00441-0376-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cee1/345787/f65bb0e03fa3/pnas00441-0375-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cee1/345787/97e0c1a4bda8/pnas00441-0376-a.jpg

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Polymerization of the ninth component of complement (C9): formation of poly(C9) with a tubular ultrastructure resembling the membrane attack complex of complement.补体第九成分(C9)的聚合:形成具有类似于补体膜攻击复合物的管状超微结构的多聚(C9)。
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本文引用的文献

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2
Analysis of solute diffusion across the C5b-9 membrane lesion of complement: evidence that individual C5b-9 complexes do not function as discrete, uniform pores.补体C5b-9膜损伤处溶质扩散分析:单个C5b-9复合物并非作为离散、均匀的孔发挥作用的证据。
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Binding of the eighth component of human complement to the soluble cytolytic complex is mediated by its beta subunit.
有或没有C9的末端补体复合物增强针对……的抗菌活性。
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Breaching the Bacterial Envelope: The Pivotal Role of Perforin-2 (MPEG1) Within Phagocytes.突破细菌包膜:吞噬细胞中穿孔素-2(MPEG1)的关键作用。
Front Immunol. 2021 Feb 22;12:597951. doi: 10.3389/fimmu.2021.597951. eCollection 2021.
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Perforin-2 Breaches the Envelope of Phagocytosed Bacteria Allowing Antimicrobial Effectors Access to Intracellular Targets.穿孔素-2 破坏吞噬细菌的包膜,使抗菌效应物能够进入细胞内靶标。
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Killing of Microbes and Cancer by the Immune System with Three Mammalian Pore-Forming Killer Proteins.免疫系统利用三种哺乳动物成孔杀伤蛋白杀灭微生物和癌细胞。
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Infect Immun. 2016 Mar 24;84(4):1083-1091. doi: 10.1128/IAI.01434-15. Print 2016 Apr.
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