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寄生虫的半胱氨酸蛋白酶抑制剂。

Cystatins of parasitic organisms.

机构信息

Department of Molecular Parasitology, Humboldt University Berlin, Germany.

出版信息

Adv Exp Med Biol. 2011;712:208-21. doi: 10.1007/978-1-4419-8414-2_13.

Abstract

The cystatin superfamily comprises several groups of protease inhibitors. In this chapter we will focus on I25 family members, which consist predominantly of the type 2 cystatins. Recently, a wealth of information on these molecules and their activities has been described. Parasite cystatins are shown to have dual functions via interaction with both parasite and host proteases. Thereby, parasite cystatins are not only essentially involved in the regulation of physiological processes during parasite development, but also represent important pathogenicity factors. Interestingly, some studies indicate that parasite cystatins evolved exceptional immuno-modulatory properties. these capacities could be exploited to interfere with unwanted immune responses in unrelated human inflammatory diseases. We highlight the different biological roles of parasite cystatins and the anticipated future developments.

摘要

半胱氨酸蛋白酶抑制剂超家族包括几个蛋白酶抑制剂家族。在本章中,我们将主要关注 I25 家族成员,它们主要由 II 型半胱氨酸蛋白酶抑制剂组成。最近,人们对这些分子及其活性的大量信息进行了描述。寄生虫半胱氨酸蛋白酶抑制剂通过与寄生虫和宿主蛋白酶的相互作用具有双重功能。因此,寄生虫半胱氨酸蛋白酶抑制剂不仅在寄生虫发育过程中对生理过程的调节至关重要,而且是重要的致病性因素。有趣的是,一些研究表明,寄生虫半胱氨酸蛋白酶抑制剂进化出了特殊的免疫调节特性。这些特性可以被利用来干扰与无关的人类炎症性疾病中不需要的免疫反应。我们强调了寄生虫半胱氨酸蛋白酶抑制剂的不同生物学作用以及预期的未来发展。

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