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Bioorthogonal Metabolic Labeling of the Virulence Factor Phenolic Glycolipid in Mycobacteria.
Guzmán, Lindsay E; Cambier, C J; Cheng, Tan-Yun; Naqvi, Kubra F; Shiloh, Michael U; Moody, D Branch; Bertozzi, Carolyn R.
Afiliação
  • Guzmán LE; Stanford Sarafan ChEM-H, Stanford University, Stanford, California 94305, United States.
  • Cambier CJ; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Cheng TY; Stanford Sarafan ChEM-H, Stanford University, Stanford, California 94305, United States.
  • Naqvi KF; Department of Chemistry, Stanford University, Stanford, California 94305, United States.
  • Shiloh MU; Brigham and Women's Hospital, Division of Rheumatology, Inflammation and Immunity, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Moody DB; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
  • Bertozzi CR; Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States.
ACS Chem Biol ; 19(3): 707-717, 2024 03 15.
Article em En | MEDLINE | ID: mdl-38442242
ABSTRACT
Surface lipids on pathogenic mycobacteria modulate infection outcomes by regulating host immune responses. Phenolic glycolipid (PGL) is a host-modulating surface lipid that varies among clinical Mycobacterium tuberculosis strains. PGL is also found in Mycobacterium marinum, where it promotes infection of zebrafish through effects on the innate immune system. Given the important role this lipid plays in the host-pathogen relationship, tools for profiling its abundance, spatial distribution, and dynamics are needed. Here, we report a strategy for imaging PGL in live mycobacteria using bioorthogonal metabolic labeling. We functionalized the PGL precursor p-hydroxybenzoic acid (pHB) with an azide group (3-azido pHB). When fed to mycobacteria, 3-azido pHB was incorporated into the cell surface, which could then be visualized via the bioorthogonal conjugation of a fluorescent probe. We confirmed that 3-azido pHB incorporates into PGL using mass spectrometry methods and demonstrated selectivity for PGL-producing M. marinum and M. tuberculosis strains. Finally, we applied this metabolic labeling strategy to study the dynamics of PGL within the mycobacterial membrane. This new tool enables visualization of PGL that may facilitate studies of mycobacterial pathogenesis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mycobacterium marinum / Mycobacterium tuberculosis Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mycobacterium marinum / Mycobacterium tuberculosis Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article