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抗补体调节蛋白H因子(β1H)的单克隆抗体。

Monoclonal antibodies against the complement control protein factor H (beta 1 H).

作者信息

Sim E, Palmer M S, Puklavec M, Sim R B

出版信息

Biosci Rep. 1983 Dec;3(12):1119-31. doi: 10.1007/BF01120205.

Abstract

Two mouse monoclonal antibodies against the human complement control protein, Factor H (beta 1H), are described. The antibodies are both IgG - gamma 1 - subclass and are directed against different epitopes on the human Factor H molecule. One of the antibodies, MRC OX 24, increases the cofactor activity of Factor H in Factor I-mediated cleavage of soluble C3b. The second antibody, MRC OX 23, which has no effect alone, reduces the increase in cofactor activity observed in the presence of the first antibody. However, MRC OX 24 inhibits the binding of 125I-labelled Factor H to surface-bound C3b (EAC3b). Again MRC OX 23 alone does not have an effect but decreases the inhibition in 125I-labelled Factor H binding to EAC3b observed with MRC OX 24. These studies show clearly that the interaction of Factor H with soluble C3b is different to its interaction with surface-bound C3b. In an indirect immunoprecipitation system using these monoclonal antibodies, single-chain molecules of 150 000 mol.wt. are specifically precipitated from human serum and also from the sera of other primates - rhesus monkey, cynomolgus monkey, and African green monkey. There was no precipitation from sera of cow, pig, sheep, chick, or rabbit. Using a radioimmunoassay with radiolabelled monoclonal MRC OX 23, the concentration of Factor H in human plasma was determined.

摘要

本文描述了两种针对人补体控制蛋白H因子(β1H)的小鼠单克隆抗体。这两种抗体均为IgG-γ1亚类,且针对人H因子分子上不同的表位。其中一种抗体MRC OX 24,可增强H因子在I因子介导的可溶性C3b裂解中的辅因子活性。第二种抗体MRC OX 23单独作用时无效应,但可降低在第一种抗体存在时观察到的辅因子活性的增加。然而,MRC OX 24可抑制125I标记的H因子与表面结合的C3b(EAC3b)的结合。同样,MRC OX 23单独作用时无效应,但可降低MRC OX 24所观察到的125I标记的H因子与EAC3b结合的抑制作用。这些研究清楚地表明,H因子与可溶性C3b的相互作用不同于其与表面结合的C3b的相互作用。在使用这些单克隆抗体的间接免疫沉淀系统中,150 000分子量的单链分子可从人血清以及其他灵长类动物——恒河猴、食蟹猴和非洲绿猴的血清中特异性沉淀出来。牛、猪、羊、鸡或兔的血清中未出现沉淀。使用放射性标记的单克隆MRC OX 23进行放射免疫测定,测定了人血浆中H因子的浓度。

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