Jaisinghani Neetika, Previti Mary L, Andrade Joshua, Askenazi Manor, Ueberheide Beatrix, Seeliger Jessica C
Department of Pharmacological Sciences, Stony Brook University, Stony Brook, NY 11794, USA.
Proteomics Laboratory, New York University Grossman School of Medicine, New York, NY 10016, USA.
Cell Chem Biol. 2024 Mar 21;31(3):523-533.e4. doi: 10.1016/j.chembiol.2023.10.013. Epub 2023 Nov 14.
The cell wall of mycobacteria plays a key role in interactions with the environment. Its ability to act as a selective filter is crucial to bacterial survival. Proteins in the cell wall enable this function by mediating the import and export of diverse metabolites, from ions to lipids to proteins. Identifying cell wall proteins is an important step in assigning function, especially as many mycobacterial proteins lack functionally characterized homologues. Current methods for protein localization have inherent limitations that reduce accuracy. Here we showed that although chemical labeling of live cells did not exclusively label surface proteins, protein tagging by the engineered peroxidase APEX2 within live Mycobacterium tuberculosis accurately identified the cytosolic and cell wall proteomes. Our data indicate that substrates of the virulence-associated Type VII ESX secretion system are exposed to the periplasm, providing insight into the currently unknown mechanism by which these proteins cross the mycobacterial cell envelope.
分枝杆菌的细胞壁在与环境的相互作用中起着关键作用。其作为选择性过滤器的能力对细菌生存至关重要。细胞壁中的蛋白质通过介导从离子到脂质再到蛋白质等多种代谢物的输入和输出实现这一功能。鉴定细胞壁蛋白是确定功能的重要一步,尤其是因为许多分枝杆菌蛋白缺乏功能特征明确的同源物。目前的蛋白质定位方法存在固有的局限性,降低了准确性。我们在此表明,虽然活细胞的化学标记并非专门标记表面蛋白,但在活的结核分枝杆菌内通过工程化过氧化物酶APEX2进行蛋白质标记可准确鉴定胞质和细胞壁蛋白质组。我们的数据表明,与毒力相关的VII型ESX分泌系统的底物暴露于周质,这为这些蛋白质穿过分枝杆菌细胞包膜的当前未知机制提供了见解。