Zig, Zag, and ’Zyme: leveraging structural biology to engineer disease resistance

IF 4.6 4区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Alexander J. McClelland, Wenbo Ma
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Abstract

Dynamic host–pathogen interactions determine whether disease will occur. Pathogen effector proteins are central players in such disease development. On one hand, they improve susceptibility by manipulating host targets; on the other hand, they can trigger immunity after recognition by host immune receptors. A major research direction in the study of molecular plant pathology is to understand effector-host interactions, which has informed the development and breeding of crops with enhanced disease resistance. Recent breakthroughs on experiment- and artificial intelligence-based structure analyses significantly accelerate the development of this research area. Importantly, the detailed molecular insight of effector–host interactions enables precise engineering to mitigate disease. Here, we highlight a recent study by Xiao et al., who describe the structure of an effector-receptor complex that consists of a fungal effector, with polygalacturonase (PG) activity, and a plant-derived polygalacturonase-inhibiting protein (PGIP). PGs weaken the plant cell wall and produce immune-suppressive oligogalacturonides (OGs) as a virulence mechanism; however, PGIPs directly bind to PGs and alter their enzymatic activity. When in a complex with PGIPs, PGs produce OG polymers with longer chains that can trigger immunity. Xiao et al. demonstrate that a PGIP creates a new active site tunnel, together with a PG, which favors the production of long-chain OGs. In this way, the PGIP essentially acts as both a PG receptor and enzymatic manipulator, converting virulence to defense activation. Taking a step forward, the authors used the PG-PGIP complex structure as a guide to generate PGIP variants with enhanced long-chain OG production, likely enabling further improved disease resistance. This study discovered a novel mechanism by which a plant receptor plays a dual role to activate immunity. It also demonstrates how fundamental knowledge, obtained through structural analyses, can be employed to guide the design of proteins with desired functions in agriculture.

Zig"、"Zag "和 "Zyme":利用结构生物学设计抗病性
宿主与病原体之间的动态相互作用决定了疾病是否会发生。病原体效应蛋白是这种疾病发展过程中的核心角色。一方面,它们通过操纵宿主靶标来提高易感性;另一方面,它们可以在被宿主免疫受体识别后触发免疫。植物分子病理学研究的一个主要方向是了解效应蛋白与宿主的相互作用,这为开发和培育抗病性更强的作物提供了依据。最近在基于实验和人工智能的结构分析方面取得的突破大大加快了这一研究领域的发展。重要的是,通过对效应器-宿主相互作用的详细分子洞察,可以进行精确的工程设计以减轻病害。在此,我们重点介绍肖等人最近的一项研究,他们描述了一种效应物-受体复合物的结构,该复合物由具有聚半乳糖醛酸酶(PG)活性的真菌效应物和植物源聚半乳糖醛酸酶抑制蛋白(PGIP)组成。PGs 可削弱植物细胞壁,并产生具有免疫抑制作用的低聚半乳糖醛酸(OGs),作为一种毒力机制;然而,PGIPs 可直接与 PGs 结合,并改变其酶活性。当 PGIP 与 PGs 复合时,PGs 会产生具有较长链的 OG 聚合物,从而引发免疫。Xiao 等人的研究表明,PGIP 与 PG 一起形成了一个新的活性位点隧道,有利于产生长链 OGs。这样,PGIP 本质上既是 PG 受体,又是酶操纵器,将毒力转化为防御激活。作者又向前迈进了一步,以 PG-PGIP 复合物结构为指导,生成了具有更强长链 OG 生成能力的 PGIP 变体,从而有可能进一步提高抗病性。这项研究发现了一种植物受体在激活免疫力方面发挥双重作用的新机制。它还展示了如何利用通过结构分析获得的基础知识来指导设计具有农业所需功能的蛋白质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
2.80%
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0
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