Nagasawa S, Ichihara C, Stroud R M
J Immunol. 1980 Aug;125(2):578-82.
We have investigated the mechanism of cleavage of C4b into C4c and C4d by the C3b inactivator (C3bINA) and revealed the formation of a nicked form of C4b as an intermediate cleavage product. The cleavage of C4b by the C3bINA was a two-step reaction. The first cleavage occurred on the alpha-chain (89,000 daltons) yielding two fragments, 73,000 daltons and 16,000 daltons. These fragments were bound to each other or to the beta or gamma chain through disulfide linkages. Therefore, an altered form of C4b, C4b', consisting of four disulfide-linked polypeptide chains with the same m.w. as C4b, was produced as an intermediate cleavage product. Subsequently, the second cleavage occurred on the alpha-chain fragment of 73,000 daltons to produce the two generally recognized fragments, C4c and C4d. In both cleavage reactions, a high m.w. cofactor protein, C4bC3bINACo, which is the same protein described as the C4 binding protein, was required, suggesting that both of the proteolytic processes are catalyzed by the C3bINA.
我们研究了C3b灭活因子(C3bINA)将C4b裂解为C4c和C4d的机制,并揭示了一种带切口形式的C4b作为中间裂解产物的形成过程。C3bINA对C4b的裂解是一个两步反应。第一步裂解发生在α链(89,000道尔顿)上,产生两个片段,73,000道尔顿和16,000道尔顿。这些片段通过二硫键彼此相连或与β链或γ链相连。因此,产生了一种改变形式的C4b,即C4b',它由四条具有与C4b相同分子量的二硫键连接的多肽链组成,作为中间裂解产物。随后,第二步裂解发生在73,000道尔顿的α链片段上,产生两个普遍认可的片段,C4c和C4d。在这两个裂解反应中,都需要一种高分子量的辅因子蛋白C4bC3bINACo,它与被描述为C4结合蛋白的蛋白相同,这表明这两个蛋白水解过程均由C3bINA催化。