Biointeractions and Crop Protection, Rothamsted Research, Hertfordshire, UK.
Department of Biology & Biochemistry, University of Bath, Claverton Down, Bath, UK.
Nat Microbiol. 2018 Apr;3(4):402-414. doi: 10.1038/s41564-018-0127-5. Epub 2018 Mar 27.
G-protein signalling pathways are involved in sensing the environment, enabling fungi to coordinate cell function, metabolism and development with their surroundings, thereby promoting their survival, propagation and virulence. G-protein-coupled receptors (GPCRs) are the largest class of cell surface receptors in fungi. Despite the apparent importance of GPCR signalling to fungal biology and virulence, relatively few GPCR-G-protein interactions, and even fewer receptor-binding ligands, have been identified. Approximately 40% of current pharmaceuticals target human GPCRs, due to their cell surface location and central role in cell signalling. Fungal GPCRs do not belong to any of the mammalian receptor classes, making them druggable targets for antifungal development. This Review Article evaluates developments in our understanding of fungal GPCR-mediated signalling, while substantiating the rationale for considering these receptors as potential antifungal targets. The need for insights into the structure-function relationship of receptor-ligand interactions is highlighted, which could facilitate the development of receptor-interfering compounds that could be used in disease control.
G 蛋白信号通路参与感知环境,使真菌能够协调细胞功能、代谢和发育与其周围环境,从而促进其生存、繁殖和毒力。G 蛋白偶联受体 (GPCR) 是真菌中最大的细胞表面受体类群。尽管 GPCR 信号对真菌生物学和毒力至关重要,但鉴定出的 GPCR-G 蛋白相互作用相对较少,甚至更少的受体结合配体。由于其位于细胞表面及其在细胞信号转导中的核心作用,目前约有 40%的现有药物针对人类 GPCR。真菌 GPCR 不属于任何哺乳动物受体类别,因此成为抗真菌药物开发的可成药靶点。本文综述评估了我们对真菌 GPCR 介导的信号转导的理解的进展,同时为将这些受体作为潜在的抗真菌靶点提供了依据。强调需要深入了解受体-配体相互作用的结构-功能关系,这有助于开发可用于疾病控制的受体干扰化合物。