Freeze-thaw activation of the complement attack phase: I. Separation of two steps in the formation of the active C--56 complex.

A Dessauer, U Rother, K Rother
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Abstract

The activation of the attack phase of C, C5-C9, is generally assumed to be dependent on the enzymes of the C activation pathways which cleave C5 into C5b and C5a. C5b will then form a complex with C6 that binds to membranes and, in the presence of C7-C9, effects cell lysis. In contrast, however, a variety of physicochemical means was found to activate C5 + C6 independently of the convertases and without apparent generation of the C5a peptide. By freezing and thawing of C5 + C6 a hemolytic C--56 activity was generated: (C--56 ).f The activation proceeded in two steps: (1) during a preincubation period of the two components the time and temperature dependent formation of an activatable intermediate was observed and (2) the intermediate C--56 could then be endowed with hemolytic activity by freezing and thawing. The intermediate as well as the activated (C--56)f complex was separated from C5 and C6 by anion exchange chromatography. While the isolated intermediate was labile, the active product after freezing and thawing was stable.

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补体攻击阶段的冻融活化:1 .活性C- 56复合物形成的两个步骤的分离。
C5- c9攻击期的激活通常被认为依赖于将C5裂解为C5b和C5a的C激活途径上的酶。然后,C5b将与C6形成复合物,与细胞膜结合,在C7-C9存在的情况下,影响细胞裂解。然而,与此相反,多种物理化学手段被发现可以独立于转化酶激活C5 + C6,并且没有明显的C5a肽的产生。通过C5 + C6的冷冻和解冻,产生溶血活性C—56:(C—56)。f激活分两步进行:(1)在两组分的预孵育期间,观察到可激活中间体的形成取决于时间和温度;(2)中间体C- 56可以通过冷冻和解冻被赋予溶血活性。用阴离子交换色谱法从C5和C6中分离出中间体和活化的(C—56)f配合物。分离的中间体是不稳定的,而冻融后的活性产物是稳定的。
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