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Liposome-mediated cellular delivery of active gp91(phox)

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  • معلومة اضافية
    • Contributors:
      TheREx; Techniques de l'Ingénierie Médicale et de la Complexité - Informatique, Mathématiques et Applications, Grenoble - UMR 5525 (TIMC-IMAG); VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF); VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF); Laboratoire d'Enzymologie (DBPC); CHU Grenoble-GREPI EA 2938; Groupe de Recherche et d’Étude du Processus Inflammatoire (TIMC-IMAG-GREPI); Grants from the 'Ministère de l'Enseignement supérieur de la Recherche et Technologie', Paris, France; the 'UFR de Médecine, Université Joseph Fourier', Grenoble, France; the 'Région Rh?'ne Alpes, programme Emergence 2003', France; the CGD Research Trust, UK; the 'Groupement des Entreprises Françaises dans la lutte contre le Cancer', délégation de Grenoble, the 'Délégation Régionale de la Recherche Clinique', CHU Grenoble, France and the Marie Curie Excellence Grant (EXT014320); (Dept of microbiology; Montana State University; Bozeman; USA
    • بيانات النشر:
      HAL CCSD, 2007.
    • الموضوع:
      2007
    • نبذة مختصرة :
      International audience; BACKGROUND: Gp91(phox) is a transmembrane protein and the catalytic core of the NADPH oxidase complex of neutrophils. Lack of this protein causes chronic granulomatous disease (CGD), a rare genetic disorder characterized by severe and recurrent infections due to the incapacity of phagocytes to kill microorganisms. METHODOLOGY: Here we optimize a prokaryotic cell-free expression system to produce integral mammalian membrane proteins. CONCLUSIONS: Using this system, we over-express truncated forms of the gp91(phox) protein under soluble form in the presence of detergents or lipids resulting in active proteins with a "native-like" conformation. All the proteins exhibit diaphorase activity in the presence of cytosolic factors (p67(phox), p47(phox), p40(phox) and Rac) and arachidonic acid. We also produce proteoliposomes containing gp91(phox) protein and demonstrate that these proteins exhibit activities similar to their cellular counterpart. The proteoliposomes induce rapid cellular delivery and relocation of recombinant gp91(phox) proteins to the plasma membrane. Our data support the concept of cell-free expression technology for producing recombinant proteoliposomes and their use for functional and structural studies or protein therapy by complementing deficient cells in gp91(phox) protein.
    • ISSN:
      1932-6203
    • الرقم المعرف:
      10.1371/journal.pone.0000856⟩
    • Rights:
      OPEN
    • الرقم المعرف:
      edsair.doi.dedup.....b336abf3785a1acb2fc33c6a821dad4e