Dessauer A, Rother U, Rother K
Acta Pathol Microbiol Immunol Scand Suppl. 1984;284:75-81.
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.
补体C5 - C9攻击阶段的激活通常被认为依赖于补体激活途径中的酶,这些酶将C5裂解为C5b和C5a。然后,C5b会与C6形成复合物,该复合物结合到细胞膜上,并在C7 - C9存在的情况下导致细胞裂解。然而,与之相反的是,人们发现多种物理化学方法可独立于转化酶激活C5 + C6,且不会明显产生C5a肽。通过对C5 + C6进行冻融,产生了溶血C56活性:(C56)f。激活过程分两步进行:(1) 在两种成分的预孵育期内,观察到了可激活中间体的时间和温度依赖性形成;(2) 然后通过冻融赋予中间体C56溶血活性。中间体以及激活后的(C56)f复合物通过阴离子交换色谱法与C5和C6分离。虽然分离出的中间体不稳定,但冻融后的活性产物是稳定的。