AbstractRecently we have shown that the free energy for pore formation induced by antimicrobial peptides contains a term representing peptide-peptide interactions mediated by membrane thinning. This many-body effect gives rise to the cooperative concentration dependence of peptide activities. Here we performed oriented circular dichroism and x-ray diffraction experiments to study the lipid dependence of this many-body effect. In particular we studied the correlation between lipid’s spontaneous curvature and peptide’s threshold concentration for pore formation by adding phosphatidylethanolamine and lysophosphocholine to phosphocholine bilayers. Previously it was argued that this correlation exhibited by magainin and melittin supported the to...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
AbstractRecently we have shown that the free energy for pore formation induced by antimicrobial pept...
AbstractAntimicrobial peptides have two binding states in a lipid bilayer, a surface state S and a p...
ABSTRACT: Antimicrobial peptides are known to form pores in cell membranes. We study this process in...
AbstractBased on very extensive studies on four peptides (alamethicin, melittin, magainin and proteg...
AbstractResearch on antimicrobial peptides is in part driven by urgent medical needs such as the ste...
AbstractBased on very extensive studies on four peptides (alamethicin, melittin, magainin and proteg...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
AbstractRecently we have shown that the free energy for pore formation induced by antimicrobial pept...
AbstractAntimicrobial peptides have two binding states in a lipid bilayer, a surface state S and a p...
ABSTRACT: Antimicrobial peptides are known to form pores in cell membranes. We study this process in...
AbstractBased on very extensive studies on four peptides (alamethicin, melittin, magainin and proteg...
AbstractResearch on antimicrobial peptides is in part driven by urgent medical needs such as the ste...
AbstractBased on very extensive studies on four peptides (alamethicin, melittin, magainin and proteg...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
Antimicrobial peptides usually kill bacteria by making their membranes permeable. Two main models (b...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...
In this work we examine the interaction between the 13-residue cationic antimicrobial peptide (AMP) ...