The use of biospecific interactions for the separation and recovery of
biomolecules is widely established, but developments in affinity-base
d separations for cell fractionation have been slow. Many of the probl
ems encountered result from applying techniques developed for molecula
r systems to cell separation with only minor modification to the condi
tions. This approach tends to ignore, or at least trivialize, the prob
lems that arise from the heterogeneous nature of a cell suspension and
the implications of cooperativity that can occur with multivalent int
eractions. This article considers how alternative protocols might be u
sed to develop more attractive cell-separation processes.