Molecular Basis for the Dynamic Strength of the Integrin α 4 β 1/VCAM-1 Interaction

• Published in: Biophysical journal 2004, Vol.87 (5), p.3470-3478
• Main Authors: Zhang, Xiaohui, Craig, Susan E., Kirby, Hishani, Humphries, Martin J., Moy, Vincent T.
• Format: Article
• Language: English
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1529/biophysj.104.045690

Intercellular adhesion mediated by integrin α 4 β 1 and vascular cell adhesion molecule-1 (VCAM-1) plays a crucial role in both the rolling and firm attachment of leukocytes onto the vascular endothelium. Essential to the α 4 β 1/VCAM-1 interaction is its mechanical strength that allows the complex to resist the large shear forces imposed by the bloodstream. Herein we employed single-molecule dynamic force spectroscopy to investigate the dynamic strength of the α 4 β 1/VCAM-1 complex. Our force measurements revealed that the dissociation of the α 4 β 1/VCAM-1 complex involves overcoming at least two activation potential barriers: a steep inner barrier and a more elevated outer barrier. The inner barrier grants the complex the tensile strength to withstand large pulling forces (>50 pN) and was attributed to the ionic interaction between the chelated Mg 2+ ion at the N-terminal A-domain of the β 1 subunit of α 4 β 1 and the carboxyl group of Asp-40 of VCAM-1 through the use of site-directed mutations. In general, additional mutations within the C-D loop of domain 1 of VCAM-1 suppressed both inner and outer barriers of the α 4 β 1/VCAM-1 complex, while a mutation at Asp-143 of domain 2 of VCAM-1 resulted in the suppression of the outer barrier, but not the inner barrier. In contrast, the outer barrier of α 4 β 1/VCAM-1 complex was stabilized by integrin activation. Together, these findings provide a molecular explanation for the functionally relevant kinetic properties of the α 4 β 1/VCAM-1 interaction.