Abstract
It is currently accepted that the biological membrane is composed of
amphiphilie lipids arranged in bilayers with functionally important proteins
embedded in, or spanning, the hydrophobic interior of the bilayer (Singer,
1977). Support for this view comes from a variety of chemical and physical
methods. Enzymatic and chemical modification reactions have established the
basic property of membrane asymmetry for lipids (Verkleij et al., 1973) and
proteins (Steck, 1978) and the results of many physical studies are most
easily interpreted in the context of structural and functional asymmetry.
Such studies often rely on the modification of biomembranes by probes;
relatively few methods exist, however, to study the transbilayer
concentration of native molecules directly. Moreover, the accessibility of
reagent or probe molecules to membrane molecules or domains, or their
distribution within or across the plane of the membrane, remain in some
instances uncertain. In such instances it is desirable to have the means to
determine their location directly by an independent method such as electron
microscopy.
Publisher
Cambridge University Press (CUP)