Antigen-receptor engagement is a complex, highly orchestrated rearrangement
of signaling molecules at, and adjacent to, the plasma membrane. Recent di
scoveries have shown that the plasma membrane itself is differentiated into
microdomains of distinct lipid constituents and that the affiliation of li
pid-modified proteins with those domains has important implications for ant
igen-receptor function. Disruption of lipid microdomains by a variety of me
thods attenuates TCR signal transduction.