• Title of article

    Structure of Bacteriocin AS-48: From Soluble State to Membrane Bound State

  • Author/Authors

    M.J. S?nchez-Barrena، نويسنده , , M. Mart??nez-Ripoll، نويسنده , , A. G?lvez، نويسنده , , E. Valdivia، نويسنده , , M. Maqueda، نويسنده , , Claudio C. V. Cruz، نويسنده , , A. Albert، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    9
  • From page
    541
  • To page
    549
  • Abstract
    The bacteriocin AS-48 is a membrane-interacting peptide, which displays a broad anti-microbial spectrum against Gram-positive and Gram-negative bacteria. The NMR structure of AS-48 at pH 3 has been solved. The analysis of this structure suggests that the mechanism of AS-48 anti-bacterial activity involves the accumulation of positively charged molecules at the membrane surface leading to a disruption of the membrane potential. Here, we report the high-resolution crystal structure of AS-48 and sedimentation equilibrium experiments showing that this bacteriocin is able to adopt different oligomeric structures according to the physicochemical environment. The analysis of these structures suggests a mechanism for molecular function of AS-48 involving a transition from a water-soluble form to a membrane-bound state upon membrane binding.
  • Keywords
    Bacteriocin , Protein Crystallography , cyclic peptide , protein–membrane interaction , cationic antibacterial peptides
  • Journal title
    Journal of Molecular Biology
  • Serial Year
    2003
  • Journal title
    Journal of Molecular Biology
  • Record number

    1243196