The past several years have seen the beginning of a shift in the way that T
CR signal transduction is studied. Although many investigators continue to
identify new molecules, particularly adaptor proteins, others have attempte
d to look at signaling events in a larger cellular context. Thus the identi
fication of distinct formations of signaling molecules at junctions between
T cells and antigen-presenting cells, the role of the cytoskeleton and the
partitioning of molecules into specialized lipid subdomains have been the
subjects of many publications. Such concepts are helping to assemble a blue
print of how the myriad adaptors and kinases fit together to effect T cell
activation.