Dipartimento di Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario "A. Gemelli" , Rome, Italy.
Dipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie - Sezione di Microbiologia, Università Cattolica del Sacro Cuore , Rome, Italy.
Virulence. 2020 Dec;11(1):898-915. doi: 10.1080/21505594.2020.1785815.
To the PE_PGRS protein subfamily belongs a group of surface-exposed mycobacterial antigens that in () H37Rv accounts to more than 65 genes, 51 of which are thought to express a functional protein. PE_PGRS proteins share a conserved structural architecture with three main domains: the N-terminal PE domain; the PGRS domain, that can vary in sequence and size and is characterized by the presence of multiple GGA-GGX amino acid repeats; the highly conserved sequence containing the GRPLI motif that links the PE and PGRS domains; the unique C-terminus end that can vary in size from few to up to ≈ 300 amino acids. genes emerged in slow-growing mycobacteria and expanded and diversified in MTBC and few other pathogenic mycobacteria. Interestingly, despite sequence homology and apparent redundancy, PE_PGRS proteins seem to have evolved a peculiar function. In this review, we summarize the actual knowledge on this elusive protein family in terms of evolution, structure, and function, focusing on the role of PE_PGRS in TB pathogenesis. We provide an original hypothesis on the role of the PE domain and propose a structural model for the polymorphic PGRS domain that might explain how so similar proteins can have different physiological functions.
PE_PGRS 蛋白亚家族属于一组表面暴露的分枝杆菌抗原,在 H37Rv 中超过 65 个基因属于该亚家族,其中 51 个基因被认为表达有功能的蛋白质。PE_PGRS 蛋白具有保守的结构架构,由三个主要结构域组成:N 端的 PE 结构域;PGRS 结构域,序列和大小可变,其特征是存在多个 GGA-GGX 氨基酸重复;高度保守的序列包含 GRPLI 基序,连接 PE 和 PGRS 结构域;独特的 C 末端,大小从几个到 ≈ 300 个氨基酸不等。这些基因在生长缓慢的分枝杆菌中出现,并在 MTBC 和其他少数致病性分枝杆菌中扩张和多样化。有趣的是,尽管存在序列同源性和明显的冗余性,但 PE_PGRS 蛋白似乎已经进化出一种特殊的功能。在这篇综述中,我们根据进化、结构和功能总结了这个难以捉摸的蛋白家族的现有知识,重点关注 PE_PGRS 在结核病发病机制中的作用。我们对 PE 结构域的作用提出了一个原始假设,并提出了一个多态性 PGRS 结构域的结构模型,该模型可能解释了如此相似的蛋白如何具有不同的生理功能。