Veyron-Churlet Romain, Locht Camille
Institut Pasteur de Lille, CHU Lille, CNRS, Inserm, Université de Lille, U1019 - UMR 8204 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France.
Pathogens. 2019 Oct 1;8(4):173. doi: 10.3390/pathogens8040173.
Studies on protein-protein interactions (PPI) can be helpful for the annotation of unknown protein functions and for the understanding of cellular processes, such as specific virulence mechanisms developed by bacterial pathogens. In that context, several methods have been extensively used in recent years for the characterization of PPI to further decipher tuberculosis (TB) pathogenesis. This review aims at compiling the most striking results based on in vivo methods (yeast and bacterial two-hybrid systems, protein complementation assays) for the specific study of PPI in mycobacteria. Moreover, newly developed methods, such as in-cell native mass resonance and proximity-dependent biotinylation identification, will have a deep impact on future mycobacterial research, as they are able to perform dynamic (transient interactions) and integrative (multiprotein complexes) analyses.
蛋白质-蛋白质相互作用(PPI)研究有助于注释未知蛋白质功能,并有助于理解细胞过程,例如细菌病原体所形成的特定毒力机制。在此背景下,近年来有几种方法被广泛用于表征PPI,以进一步解读结核病(TB)的发病机制。本综述旨在汇总基于体内方法(酵母双杂交和细菌双杂交系统、蛋白质互补分析)对分枝杆菌中PPI进行特异性研究的最显著结果。此外,新开发的方法,如细胞内天然质谱共振和邻近依赖性生物素化鉴定,将对未来的分枝杆菌研究产生深远影响,因为它们能够进行动态(瞬时相互作用)和整合(多蛋白复合物)分析。