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J. Biol. Chem., Vol. 255, Issue 17, 8015-8018, 09, 1980
A Huang, L Huang and SJ Kennel
Monoclonal antibody to the mouse histocompatibility antigen, H-2k, was
derivatized with palmitic acid using an activated ester of N-
hydroxysuccinimide. About 70% of the resulting amphipathic antibody could
be incorporated into liposomes by a detergent-dialysis method. The
antibody-bound liposomes were about 900 A in diameter and were
heterogeneous in terms of the number of antibody molecules per liposome.
These liposomes showed specific binding affinity to mouse L- 929 cells
(H-2k), but not to A-31 cells (H-2d), whereas native liposomes showed no
detectable binding to either cell type. The specific binding of
anti-H-2k-bound liposomes to L-929 cells could be blocked by a
preincubation of cells with an excess of free, underivatized anti-H-2k
antibody but not by normal mouse IgG. Using a fluorescent phospholipid,
liposomes containing anti-H-2k specifically labeled L-929 cells but not
A-31 cells in a mixed culture. Liposomes containing normal mouse IgG did
not significantly label either cell type. These results clearly
demonstrated the effectiveness of the monoclonal antibody for liposome
targeting.
Monoclonal antibody covalently coupled with fatty acid. A reagent for in vitro liposome targeting
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