A general method for measuring interaction of Liposome-protein (or potentia
lly small molecules) was developed. This method utilizes biotinylated lipos
omes to incubate with interactants. Streptavidin-coated paramagnetic resins
were then added and the liposomes (along with bound materials) can be quic
kly separated under a magnetic field or by low speed centrifugation. Subseq
uently, concentration of unbound materials tin the supernatants) can be dir
ectly determined. The described method is particularly useful for proteins
or compounds that are not very soluble under certain assay conditions. (C)
1999 Elsevier Science BN. All rights reserved.