دورية أكاديمية

A truncated lipoglycan from mycobacteria with altered immunological properties

التفاصيل البيبلوغرافية
العنوان: A truncated lipoglycan from mycobacteria with altered immunological properties
المؤلفون: Birch, H., Alderwick, L., Appelmelk, B., Maaskant, J., Bhatt, A., Singh, A., Nigou, J., Eggeling, L., Geurtsen, J., Besra, G.
المصدر: Proceedings of the National Academy of Sciences of the United States of America 107, 2634 - 26390 (2010). doi:10.1073/pnas.0915082107
بيانات النشر: Academy
سنة النشر: 2010
المجموعة: Forschungszentrum Jülich: JuSER (Juelich Shared Electronic Resources)
مصطلحات موضوعية: info:eu-repo/classification/ddc/000, Antigens, Bacterial: chemistry, Bacterial: immunology, Bacterial: metabolism, Antitubercular Agents: pharmacology, Bacterial Proteins: chemistry, Bacterial Proteins: genetics, Bacterial Proteins: metabolism, Cell Line, Tumor, Electrophoresis, Polyacrylamide Gel, Enzyme-Linked Immunosorbent Assay, Ethambutol: pharmacology, Humans, Interleukin-8: metabolism, Lipopolysaccharides: chemistry, Lipopolysaccharides: immunology, Lipopolysaccharides: metabolism, Magnetic Resonance Spectroscopy, Mutation, Mycobacterium smegmatis: drug effects, Mycobacterium smegmatis: genetics, Mycobacterium smegmatis: metabolism, Pentosyltransferases: chemistry, Pentosyltransferases: genetics, Pentosyltransferases: metabolism, Toll-Like Receptor 2: metabolism, Tumor Necrosis Factor-alpha: metabolism
جغرافية الموضوع: DE
الوصف: Maintenance of cell-wall integrity in Mycobacterium tuberculosis is essential and is the target of several antitubercular drugs. For example, ethambutol targets arabinogalactan and lipoarabinomannan (LAM) biosynthesis through the inhibition of several arabinofuranosyltransferases. Apart from their role in cell-wall integrity, mycobacterial LAMs also exhibit important immunomodulatory activities. Here we report the isolation and detailed structural characterization of a unique LAM molecule derived from Mycobacterium smegmatis deficient in the arabinofuranosyltransferase AftC (AftC-LAM). This mutant LAM expresses a severely truncated arabinan domain completely devoid of 3,5-Araf-branching residues, revealing an intrinsic involvement of AftC in the biosynthesis of LAM. Furthermore, we found that ethambutol efficiently inhibits biosynthesis of the AftC-LAM arabinan core, unambiguously demonstrating the involvement of the arabinofuranosyltransferase EmbC in early stages of LAM-arabinan biosynthesis. Finally, we demonstrate that AftC-LAM exhibits an enhanced proinflammatory activity, which is due to its ability to activate Toll-like receptor 2 (TLR2). Overall, our efforts further describe the mechanism of action of an important antitubercular drug, ethambutol, and demonstrate a role for specific arabinofuranosyltransferases in LAM biosynthesis. In addition, the availability of sufficient amounts of chemically defined wild-type and isogenic truncated LAMs paves the way for further investigations of the structure-function relationship of TLR2 activation by mycobacterial lipoglycans.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/issn/0027-8424; info:eu-repo/semantics/altIdentifier/pmid/pmid:20133807; info:eu-repo/semantics/altIdentifier/wos/WOS:000274408100050; https://juser.fz-juelich.de/record/8882Test; https://juser.fz-juelich.de/search?p=id:%22PreJuSER-8882%22Test
الإتاحة: https://doi.org/10.1073/pnas.0915082107Test
https://juser.fz-juelich.de/record/8882Test
https://juser.fz-juelich.de/search?p=id:%22PreJuSER-8882%22Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.F64F6E7E
قاعدة البيانات: BASE