We describe affinity partitioning as a preparative method for membrane
s and membraneous structures such as organelles, cells, and viruses. B
iospecific affinity partitioning is carried out in aqueous polymer two
-phase systems, commonly with polyethylene glycol and dextran as phase
polymers, in an environment compatible with membrane structures. Idea
lly, two-phase conditions are chosen to partition the bulk of membrane
material into one phase, while the affinity ligand, conjugated to the
second phase polymer, will selectively pull the membranes to be isola
ted into this phase. Suitable ligands include lectins, antibodies, and
receptor-specific agents. Because the method has so far been used suc
cessfully in rather few instances, all using high ligand receptor dens
ities in target membranes, the discussion focuses on factors to be con
sidered when developing affinity partitioning conditions using new lig
ands.