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Richard M. Epand

Researcher at McMaster University

Publications -  521
Citations -  26937

Richard M. Epand is an academic researcher from McMaster University. The author has contributed to research in topics: Membrane & Peptide. The author has an hindex of 80, co-authored 515 publications receiving 25125 citations. Previous affiliations of Richard M. Epand include Brigham Young University & University of Edinburgh.

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Effects of viral chemotherapeutic agents on membrane properties. Studies of cyclosporin A, benzyloxycarbonyl-D-Phe-L-Phe-Gly and amantadine.

TL;DR: Three antiviral agents inhibited myelin basic protein-induced membrane fusion when present at low concentrations in the membrane when the mechanism by which these agents affect membrane properties was investigated.
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The effect of free fatty acids on the thermotropic phase transition of dimyristoyl glycerophosphocholine.

TL;DR: The effects of the very long chain fatty acids, arachidic and behenic appears to be similar to those of cholesterol in that they cause a broadening of the phase Transition with a lowering of the transition enthalpy but have little effect on the temperature at which the phase transition occurs.
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Lipid clustering by three homologous arginine-rich antimicrobial peptides is insensitive to amino acid arrangement and induced secondary structure.

TL;DR: This work shows the insensitivity of phase segregation to the specific arrangement of the cationic charges in the peptide sequence as well as to their tendency to form different secondary structures and establishes the role of anionic lipid clustering in the presence of zwitterionic lipids in determining antimicrobial selectivity.
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Promotion of hexagonal phase formation and lipid mixing by fatty acids with varying degrees of unsaturation.

TL;DR: A series of C18 and C22 fatty acids, with varying degrees of unsaturation, were tested for their ability to alter the bilayer to hexagonal phase transition temperature of dielaidoylphosphatidylethanolamine mixtures and found that increasing unsaturation of the fatty acid generally increased theirhexagonal phase-forming ability.
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A "release" protocol for isothermal titration calorimetry.

TL;DR: A general formula is derived for modeling ITC titration heats in both binding and partitioning systems that allows for the modeling of the classic incorporation or binding protocols, as well as of new protocols assessing the release of solute from previously solute-loaded vesicles upon dilution.