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眼镜蛇毒液因子:结构、功能与治疗性补体耗竭的人源化。

Cobra venom factor: Structure, function, and humanization for therapeutic complement depletion.

机构信息

Cancer Research Center of Hawaii, University of Hawaii at Manoa, 1236 Lauhala Street, Honolulu, HI 96813, USA.

出版信息

Toxicon. 2010 Dec 15;56(7):1198-222. doi: 10.1016/j.toxicon.2010.04.007. Epub 2010 Apr 22.

Abstract

Cobra venom factor (CVF) is the complement-activating protein in cobra venom. This manuscript reviews the structure and function of CVF, how it interacts with the complement system, the structural and functional homology to complement component C3, and the use of CVF as an experimental tool to decomplement laboratory animals to study the functions of complement in host defense and immune response as well as in the pathogenesis of diseases. This manuscript also reviews the recent progress in using the homology between CVF and C3 to study C3 structure and function, and to develop human C3 derivatives with the complement-depleting function of CVF. These human C3 derivatives represent humanized CVF, and are a conceptually different concept for pharmacological intervention of the complement system, therapeutic complement depletion. The use of humanized CVF for therapeutic complement depletion in several pre-clinical models of human diseases is also reviewed.

摘要

眼镜蛇毒因子(CVF)是眼镜蛇毒液中的补体激活蛋白。本文综述了 CVF 的结构和功能,它与补体系统的相互作用,与补体成分 C3 的结构和功能同源性,以及将 CVF 用作实验工具对实验动物进行去补体,以研究补体在宿主防御和免疫反应以及疾病发病机制中的功能。本文还综述了利用 CVF 与 C3 之间的同源性研究 C3 结构和功能,以及开发具有 CVF 补体耗竭功能的人 C3 衍生物的最新进展。这些人 C3 衍生物代表了对补体系统进行药理学干预的人源化 CVF,是治疗性补体耗竭的概念性不同概念。还综述了在几种人类疾病的临床前模型中使用人源化 CVF 进行治疗性补体耗竭的情况。

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