Many cell-cell and cell-matrix interactions depend upon the engagement
of specific ligands by members of the integrin family of cell-adhesio
n receptors. In concert with the identification of new integrins, the
number of integrin ligands continues to expand dramatically. The diver
sity of the integrin ligands bridges many areas of cell and molecular
biology. Ligand recognition by integrins requires not only the presenc
e of the cognate primary sequence within an appropriate secondary stru
cture, but also the correct tertiary and quaternary structure of the l
igand. Presentation of an 'activated' ligand sequence to specific cont
act sites within the integrin under specified divalent-cation conditio
ns is necessary for a productive and high-affinity interaction.