{Reference Type}: Journal Article
{Title}: Proteomics from compartment-specific APEX2 labeling in Mycobacterium tuberculosis reveals Type VII secretion substrates in the cell wall.
{Author}: Jaisinghani N;Previti ML;Andrade J;Askenazi M;Ueberheide B;Seeliger JC;
{Journal}: Cell Chem Biol
{Volume}: 31
{Issue}: 3
{Year}: 2024 Mar 21
{Factor}: 9.039
{DOI}: 10.1016/j.chembiol.2023.10.013
{Abstract}: 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.