Effects of general anesthesia can be controllable by the ambient pressure. We perform molecular dynamics simulations for a 1-palmitoyl-2-oleoyl phosphatidylethanolamine lipid bilayer with or without xenon molecules by changing the pressure to elucidate the mechanism of the pressure reversal of general anesthesia. According to the diffusive nature of xenon molecules in the lipid bilayer, a decrease in the orientational order of the lipid tails, an increase in the area and volume per lipid molecule, and an increase in the diffusivity of lipid molecules are observed. We show that the properties of the lipid bilayer with xenon molecules at high pressure come close to those without xenon molecules at 0.1 MPa. Furthermore, we find that xenon mole...
AbstractWe report a 1.4-ns constant-pressure molecular dynamics simulation of cholesterol at 12.5 mo...
AbstractThe structural perturbations of the fully hydrated dimyristoyl-phosphatidylcholine bilayer i...
ABSTRACT To gain insights into the molecular level mechanism of drug action at the membrane site, we...
We report the initial findings of 100 ns molecular dynamics simulations of the role of cellular memb...
Molecular dynamics simulations of the fully hydrated neat dipalmitoylphosphatidylcholine (DPPC) memb...
AbstractThe suggestion by Robert Cantor, that drug-induced pressure changes in lipid bilayers can ch...
Since almost all biologically relevant cell membranes are formed by phospholipid bilayers, the inves...
Using a combination of high pressure wide angle X-ray scattering experiments and molecular dynamics ...
International audienceIn this work, we performed computer simulations of halothane embedded in a ful...
The change in partial molar volume (PMV) accompanying the xenon-lysozyme binding was investigated fo...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
AbstractTo gain insights into the molecular level mechanism of drug action at the membrane site, we ...
International audienceExperiments have shown that general anaesthetics lose their efficacy at pressu...
AbstractWe report a 1.4-ns constant-pressure molecular dynamics simulation of cholesterol at 12.5 mo...
AbstractThe structural perturbations of the fully hydrated dimyristoyl-phosphatidylcholine bilayer i...
ABSTRACT To gain insights into the molecular level mechanism of drug action at the membrane site, we...
We report the initial findings of 100 ns molecular dynamics simulations of the role of cellular memb...
Molecular dynamics simulations of the fully hydrated neat dipalmitoylphosphatidylcholine (DPPC) memb...
AbstractThe suggestion by Robert Cantor, that drug-induced pressure changes in lipid bilayers can ch...
Since almost all biologically relevant cell membranes are formed by phospholipid bilayers, the inves...
Using a combination of high pressure wide angle X-ray scattering experiments and molecular dynamics ...
International audienceIn this work, we performed computer simulations of halothane embedded in a ful...
The change in partial molar volume (PMV) accompanying the xenon-lysozyme binding was investigated fo...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
The molecular mechanism of general anesthesia is still a controversial issue. Direct effect by linki...
AbstractTo gain insights into the molecular level mechanism of drug action at the membrane site, we ...
International audienceExperiments have shown that general anaesthetics lose their efficacy at pressu...
AbstractWe report a 1.4-ns constant-pressure molecular dynamics simulation of cholesterol at 12.5 mo...
AbstractThe structural perturbations of the fully hydrated dimyristoyl-phosphatidylcholine bilayer i...
ABSTRACT To gain insights into the molecular level mechanism of drug action at the membrane site, we...