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[人补体替代途径的激活(作者译)]

[Activation of the alternative pathway of human complement (author's transl)].

作者信息

Kazatchkine M, Fischer E, Nydegger U

出版信息

Ann Immunol (Paris). 1982 Mar-Apr;133C(2):181-8.

PMID:7051949
Abstract

The C3 amplification convertase of human complement, C3b, Bb, is assembled on biological surfaces by the interaction of the alternative pathway proteins B, D and P with cell-bound C3b. Convertase formation is modulated by the action of the regulatory proteins H and I. On activating surfaces of the alternative pathway, C3b, Bb is relatively resistant to regulation by H. In contrast, non-activating surfaces exhibit surface characteristics such as high content in membrane-associated sialic acid or heparin-related material which increase the interaction of H with cell-bound C3b. Thus, finely tuned molecular interactions allow the alternative pathway to function as a major recognition and effector system for natural defence.

摘要

人类补体的C3放大转化酶C3b、Bb,是通过替代途径蛋白B、D和P与细胞结合的C3b相互作用在生物表面组装而成的。转化酶的形成受调节蛋白H和I的作用调控。在替代途径的激活表面,C3b、Bb相对不易受H的调节。相反,非激活表面具有诸如膜相关唾液酸或肝素相关物质含量高的表面特征,这会增加H与细胞结合的C3b的相互作用。因此,精细调节的分子相互作用使替代途径能够作为天然防御的主要识别和效应系统发挥作用。

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