TY - JOUR
T1 - Analysis of the binding site on Intercellular Adhesion Molecule 3 for the Leukocyte Integrin Lymphocyte Function Antigen-1.C.
AU - Buckley, Christopher
PY - 1995/1
Y1 - 1995/1
N2 - Intercellular adhesion molecule 3 (ICAM-3, CD50) is a member of the immunoglobulin superfamily and is a constitutively expressed ligand for the leukocyte integrin LFA-1 (CD11a/CD18). ICAM-3 is expressed at high levels by all resting leukocyte populations and antigen presenting cells and is a major ligand for LFA-1 in the resting immune system. ICAM-3 is a signal transducer and may play a key role in initiating immune responses. Mutant ICAM-3 Fc-chimeric proteins were quantitatively analyzed for their ability to bind COS cells expressing human LFA-1. The LFA-1-binding site on ICAM-3 is located in the N-terminal 2 Ig domains. Domains 3-5 do not significantly contribute to adhesion. The binding site has been further resolved by rational targeting of 14 point mutations throughout domains 1 and 2, coupled with modeling studies. Within domain 1 a cluster of residues (GluGraphic, LeuGraphic, SerGraphic, and GlnGraphic), that are predicted to lie on the CC′FG face of the Ig fold, play a dominant role in LFA-1 binding.
AB - Intercellular adhesion molecule 3 (ICAM-3, CD50) is a member of the immunoglobulin superfamily and is a constitutively expressed ligand for the leukocyte integrin LFA-1 (CD11a/CD18). ICAM-3 is expressed at high levels by all resting leukocyte populations and antigen presenting cells and is a major ligand for LFA-1 in the resting immune system. ICAM-3 is a signal transducer and may play a key role in initiating immune responses. Mutant ICAM-3 Fc-chimeric proteins were quantitatively analyzed for their ability to bind COS cells expressing human LFA-1. The LFA-1-binding site on ICAM-3 is located in the N-terminal 2 Ig domains. Domains 3-5 do not significantly contribute to adhesion. The binding site has been further resolved by rational targeting of 14 point mutations throughout domains 1 and 2, coupled with modeling studies. Within domain 1 a cluster of residues (GluGraphic, LeuGraphic, SerGraphic, and GlnGraphic), that are predicted to lie on the CC′FG face of the Ig fold, play a dominant role in LFA-1 binding.
U2 - 10.1074/jbc.270.2.877
DO - 10.1074/jbc.270.2.877
M3 - Article
SN - 0021-9258
VL - 270
SP - 877
EP - 884
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
ER -