The existence of an in-plane domain structure in biological membranes
raises the question of the physiological function, if any, of this str
ucture. One important function may be to enhance or limit the equilibr
ium poise and rates of in-plane reactions through control by the cell
of the percolation properties of the domain system. At low average dom
ain occupancy by reactants or interactants, which must be the case for
most biological membrane components, moving the domain system from co
nnection to disconnection has marked effects on the apparent equilibri
um poise and the rates of membrane-confined reactions. This conclusion
is based on computer modelling of the effects of disconnection/connec
tion of nine types of bimolecular in-plane reactions. Using the phase
structure and percolation properties of two-component, two-phase phosp
holipid bilayers, it is possible to examine experimentally homo- and h
eterodimeriztion reactions, and enzyme-catalysed reactions in-plane as
well as the effects of a transmembrane peptide on these systems. Thes
e theoretical and experimental studies suggest that percolation effect
s may be physiologically important in biological membranes. Whether th
is is in fact the case remains to be demonstrated.