We develop a theory to model the interactions between an amphiphilic c
opolymer and a bilayer. The copolymer is represented as a Gaussian cha
in, which contains an alternating arrangement of hydrophobic and hydro
philic sites along the length of the chain. The bilayer is modeled as
a hydrophobic layer embedded in a hydrophilic environment. We use the
transfer matrix technique to determine the polymer density profiles an
d the phase diagram for this system. Two distinct phases are observed.
In one phase, the copolymer is localized at the surface or within the
bilayer. In the second phase, the polymer is unbound or ''delocalized
.'' There is a continuous transition between the two phases. We also d
etermine the scaling behavior for the density profiles. The scaling ex
ponents agree with our analytical arguments. We discuss the implicatio
ns of our findings on designing copolymers that can act as adhesives o
r macromolecular surfactants.