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
Link To Document :
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