Suppr超能文献

免疫复合物介导的经典补体途径激活。

Immune complex mediated activation of the classical complement pathway.

作者信息

Borsos T

机构信息

Department of Pathology, Uniformed Services University of the Health Sciences, Bethesda MD 20814-4799.

出版信息

Behring Inst Mitt. 1989 Jul(84):93-101.

PMID:2478118
Abstract

The activation of classical C pathway by immune complexes depends on the binding and activation of C1, the first component of C. The Ig in the complex must be of the right class and in the right configuration to accomplish the conversion of precursor (zymogen) C1s to C1s, the active enzyme, whose substrates are C4 and C2. The primary question discussed in this paper is evidence that indicates that epitope distribution and density is a major factor in controlling the configuration of antibodies which in turn controls the activation of bound C1. This evidence confirms earlier findings that binding of C1 is a necessary but not sufficient condition for activating C1.

摘要

免疫复合物对经典补体途径的激活取决于补体第一成分C1的结合与激活。复合物中的免疫球蛋白必须具有合适的类别和构型,才能实现前体(酶原)C1s向活性酶C1s的转化,C1s的底物是C4和C2。本文讨论的主要问题是有证据表明,表位分布和密度是控制抗体构型的主要因素,而抗体构型又反过来控制结合的C1的激活。这一证据证实了早期的发现,即C1的结合是激活C1的必要但不充分条件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验