Purification of a human serum protein ("factor E") which enhances cobra venom factor-induced indirect lysis. Identification with the fifth component of complement.

R Lynen, W Vogt, G Schmidt, L Dieminger
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Abstract

Complexes formed of Cobra venom factor (CVF) and activated factor B (B) by interaction of CVF and B with trypsin or factor D are capable of activating the third and fifth complement component. When incubated with sheep or guinea pig red cells and guinea pig serum in the presence of EDTA, these CVFB complexes produce "indirect lysis". Addition of a human serum factor, earlier designated as factor E (6), greatly enhances the efficiency of this lytic system. The component with this activity has been purified to homogeneity (disc and immunoelectrophoresis). In chromatographic fractionations it was inseparable from the fifth complement component, it was inactivated by and reacted with several anti-C5 antisera, and kinetics of inactivation by heat (56 degrees C) and trypsin were the same for factor E and hemolytic C5 activities. It is concluded that factor E is the fifth component of human complement. Guinea pig C5 is not capable of supporting indirect lysis in a comparable manner, for as yet unknown reasons. Some possible explanations are discussed.

纯化人血清蛋白(“因子E”),增强眼镜蛇毒液因子诱导的间接裂解。与补语第五成分的识别。
眼镜蛇毒因子(CVF)和活化因子B (B)与胰蛋白酶或因子D相互作用形成的复合物能够激活第三和第五补体成分。当与羊或豚鼠红细胞和豚鼠血清在EDTA存在下孵育时,这些CVFB复合物产生“间接裂解”。添加人血清因子,早期被指定为因子E(6),大大提高了该溶解系统的效率。具有该活性的组分经圆盘电泳和免疫电泳均质纯化。在色谱分离中,它与第五补体组分不可分离,它被几种抗C5抗血清灭活并与之反应,并且在热(56℃)和胰蛋白酶的灭活动力学中,因子E和溶血C5活性是相同的。结论:因子E是人体补体的第五成分。由于尚不清楚的原因,豚鼠C5不能以类似的方式支持间接裂解。讨论了一些可能的解释。
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