The surface expansion that is induced by the lateral pressure in the brush
region of lipid membranes containing grafted polymers is deduced from the s
caling and mean-field theories for the polymer brush, together with the equ
ation of state for a lipid monolayer at the equivalence pressure with fluid
lipid bilayers. Depending on the length and mole fraction of the polymer l
ipid, the membrane expansion can be appreciable. Direct experimental eviden
ce for this lateral expansion comes from recent spin-label measurements wit
h lipid membranes containing poly(ethylene glycol)-grafted lipids. The expa
nsion in lipid area modifies the elastic constants of the polymer-grafted m
embranes in a way that opposes the direct elastic response of the polymer i
tself. Calculations as a function of polymer lipid content indicate that th
e net change in isothermal area expansion modulus of the membrane is negati
ve but small, in contrast to previous predictions. A similar situation appl
ies to the curvature elastic moduli of membranes containing short polymer l
ipids. For longer polymer lipids, however, the direct contribution of the p
olymer brush to the bending elastic constants dominates, and the increase i
n bending moduli with increasing polymer lipid content rapidly exceeds the
basal values of the bare lipid membrane. The spontaneous (or intrinsic) cur
vature of the component monolayer of polymer lipid-containing membranes is
calculated for the first time. The polymer brush contribution to spontaneou
s curvature scales quadratically with the polymer length, and at least quad
ratically with the mole fraction of polymer lipid.