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插队:细菌 III 型效应蛋白酶对植物免疫的操纵。

Cutting the line: manipulation of plant immunity by bacterial type III effector proteases.

机构信息

Department of Biology, Maynooth University, Maynooth, County Kildare, Ireland.

Central Institute for Engineering, Electronics and Analytics, ZEA-3, Forschungszentrum Jülich, Jülich, Germany.

出版信息

J Exp Bot. 2021 Apr 13;72(9):3395-3409. doi: 10.1093/jxb/erab095.

Abstract

Pathogens and their hosts are engaged in an evolutionary arms race. Pathogen-derived effectors promote virulence by targeting components of a host's innate immune system, while hosts have evolved proteins that sense effectors and trigger a pathogen-specific immune response. Many bacterial effectors are translocated into host cells using type III secretion systems. Type III effector proteases irreversibly modify host proteins by cleavage of peptide bonds and are prevalent among both plant and animal bacterial pathogens. In plants, the study of model effector proteases has yielded important insights into the virulence mechanisms employed by pathogens to overcome their host's immune response, as well as into the mechanisms deployed by their hosts to detect these effector proteases and counteract their effects. In recent years, the study of a larger number of effector proteases, across a wider range of pathogens, has yielded novel insights into their functions and recognition. One key limitation that remains is the lack of methods to detect protease cleavage at the proteome-wide level. We review known substrates and mechanisms of plant pathogen type III effector proteases and compare their functions with those of known type III effector proteases of mammalian pathogens. Finally, we discuss approaches to uncover their function on a system-wide level.

摘要

病原体及其宿主之间存在着一场进化军备竞赛。病原体衍生的效应子通过靶向宿主固有免疫系统的成分来促进毒力,而宿主则进化出了能够感知效应子并触发针对病原体的特异性免疫反应的蛋白质。许多细菌效应子通过 III 型分泌系统被转运到宿主细胞中。III 型效应子蛋白酶通过切割肽键不可逆地修饰宿主蛋白,并且在植物和动物细菌病原体中都很普遍。在植物中,对模型效应子蛋白酶的研究为病原体用来克服宿主免疫反应的毒力机制以及宿主用来检测这些效应子蛋白酶并抵消其作用的机制提供了重要的见解。近年来,对更多的效应子蛋白酶的研究,跨越了更广泛的病原体范围,为它们的功能和识别提供了新的见解。一个仍然存在的关键限制是缺乏在全蛋白质组水平上检测蛋白酶切割的方法。我们回顾了植物病原体 III 型效应子蛋白酶的已知底物和机制,并将它们的功能与哺乳动物病原体的已知 III 型效应子蛋白酶的功能进行了比较。最后,我们讨论了在系统水平上揭示其功能的方法。

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