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Biophys J, July 2001, p. 184-195, Vol. 81, No. 1
Department of Biophysical Chemistry, Biocenter of the University of Basel, CH-4056 Basel, Switzerland
The area balance or imbalance between the inner and outer
monolayer of biological membranes is a key parameter for driving shape
changes (including exo and endocytosis) and controlling the bilayer
curvature stress. The asymmetric incorporation of a drug or biological
agent interferes with these processes, and the subsequent stress may
lead to a membrane permeation or permeabilization. A main goal of this
study is to introduce new methods to characterize such phenomena using
isothermal titration calorimetry. POPC unilamellar vesicles and a
series of alkyl maltosides are used as model systems; the
unilamellarity was checked by NMR with the shift reagent
Pr3+. The free energy, enthalpy, and entropy associated
with the asymmetry stress are estimated by comparing partitioning data
of uptake versus release assays. The asymmetry stress is of enthalpic
nature and somewhat reduced by entropic effects. Stimulated membrane permeation occurs at a mean maltoside-to-lipid ratio of ~0.2, which
corresponds to an apparent area asymmetry of ~30% and a limiting
free energy of the order of 2 kJ/mol of maltoside. Membrane solubilization to coexisting micelles proceeds at mole ratios of
~0.73, 0.81, and 0.88 (C12-, C13-, and
C14-maltoside, respectively). Experiments with vesicles
pre-loaded with surfactant in both monolayers provide evidence that the
translocation threshold is controlled by the asymmetrically
incorporated surfactant, whereas the onset of solubilization depends on
the total surfactant content in the membrane. Free copies of the uptake
and release fitting script including instructions are available upon
request to heerklotz{at}gmx.net.
Biophys J, July 2001, p. 184-195, Vol. 81, No. 1
© 2001 by the Biophysical Society 0006-3495/01/07/184/12 $2.00
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