Interview for Faculty Position
Dynamic Strength of Lipid Membranes Exposed to
Antimicrobial Peptides
Benjamin A. Smith
Departments of Physics and Pathology University of
British Columbia
Many dynamic functions of cellular membranes and membrane-associated proteins
are critically regulated by the composition and material properties of
the lipid bilayer. To understand such regulatory mechanisms we must first
identify the molecular determinants of bilayer elastic strength, permeability
and stability under dynamic stress (both physical and chemical). I will show
how advanced techniques of micropipette aspiration can probe the kinetic
process of membrane failure, understood via a simple model of nucleation and
growth of a single aqueous pore in the fluid lipid bilayer. Antimicrobial
peptides of the innate immune defense system induce a dramatic weakening
of the bilayers dynamic strength, quantified with extreme sensitivity
(1:10000 peptide:lipids) by a reduction in pore edge energy. Alternatively,
cholesterol provides a protective resistance to host (eukaryotic) membranes
against the potentially toxic effects of these novel antibiotics. These
studies employ thermodynamic models, statistical mechanics, and kinetic
reaction rate theory to describe biological function and therefore should
be of interest to the broad scientific community.
Friday, February 22nd 2008, 14:30
Ernest Rutherford Physics Building, R.E. Bell Conference Room (room 103)
|