Proteomic Analysis of the Mycobacterium tuberculosis Outer Membrane for Potential Implications in Uptake of Small Molecules

• Published in: ACS infectious diseases 2024-03, Vol.10 (3), p.890-906
• Main Authors: Palande, Aseem, Patil, Saniya, Veeram, Anjali, Sahoo, Soumya Swastik, Lodhiya, Tejan, Maurya, Pankaj, Muralikrishnan, Balaji, Chugh, Jeetender, Mukherjee, Raju
• Format: Article
• Language: English
• Subjects: Anti-Bacterial Agents - metabolism; Humans; Membrane Proteins - metabolism; Mycobacterium tuberculosis - genetics; Mycobacterium tuberculosis - metabolism; Proteomics; Tuberculosis - microbiology
• ISSN: 2373-8227; 2373-8227
• DOI: 10.1021/acsinfecdis.3c00517

Increased resistance to current antimycobacterial agents and a potential bias toward relatively hydrophobic chemical entities highlight an urgent need to understand how current anti-TB drugs enter the tubercle bacilli. While inner membrane proteins are well-studied, how small molecules cross the impenetrable outer membrane remains unknown. Here, we employed mass spectrometry-based proteomics to show that octyl-β-d-glucopyranoside selectively extracts the outer membrane proteins of Mycobacterium tuberculosis. Differentially expressed proteins between nutrient-replete and nutrient-depleted conditions were enriched to identify proteins involved in nutrient uptake. We demonstrate cell surface localization of seven new proteins using immunofluorescence and show that overexpression of the proteins LpqY and ProX leads to hypersensitivity toward streptomycin, while overexpression of SubI, SpmT, and Rv2041 exhibited higher membrane permeability, assessed through an EtBr accumulation assay. Further, proton NMR metabolomics suggests the role of six outer membrane proteins in glycerol uptake. This study identifies several outer membrane proteins that are involved in the permeation of small hydrophilic molecules and are potential targets for enhancing the uptake and efficacy of anti-TB drugs.