5 research outputs found
Free energy barrier for melittin reorientation from a membrane-bound state to a transmembrane state
An important step in a phospholipid membrane pore formation by melittin
antimicrobial peptide is a reorientation of the peptide from a surface into a
transmembrane conformation. In this work we perform umbrella sampling
simulations to calculate the potential of mean force (PMF) for the
reorientation of melittin from a surface-bound state to a transmembrane state
and provide a molecular level insight into understanding peptide and lipid
properties that influence the existence of the free energy barrier. The PMFs
were calculated for a peptide to lipid (P/L) ratio of 1/128 and 4/128. We
observe that the free energy barrier is reduced when the P/L ratio increased.
In addition, we study the cooperative effect; specifically we investigate if
the barrier is smaller for a second melittin reorientation, given that another
neighboring melittin was already in the transmembrane state. We observe that
indeed the barrier of the PMF curve is reduced in this case, thus confirming
the presence of a cooperative effect