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. 2001 Nov;81(5):2743–2751. doi: 10.1016/S0006-3495(01)75917-6

Kinetics of membrane adhesion mediated by ligand-receptor interaction studied with a biomimetic system.

A Boulbitch 1, Z Guttenberg 1, E Sackmann 1
PMCID: PMC1301741  PMID: 11606287

Abstract

We report the first measurement of the kinetics of adhesion of a single giant vesicle controlled by the competition between membrane-substrate interaction mediated by ligand-receptor interaction, gravitation, and Helfrich repulsion. To model the cell-tissue interaction, we doped the vesicles with lipid-coupled polymers (mimicking the glycocalix) and the reconstituted ligands selectively recognized by alpha(IIb)beta(3) integrin-mediating specific attraction forces. The integrin was grafted on glass substrates to act as a target cell. The adhesion of the vesicle membrane to the integrin-covered surface starts with the spontaneous formation of a small (approximately 200 nm) domain of tight adhesion, which then gradually grows until the whole adhesion area is in the state of tight adhesion. The time of adhesion varies from few tens of seconds to about one hour depending on the ligand and lipopolymer concentration. At small ligand concentrations, we observed the displacement xi of the front of tight adhesion following the square root law xi approximately t(1/2), whereas, at high concentrations, we found a linear law xi approximately t. We show both experimentally and theoretically that the t(1/2)-regime is dominated by diffusion of ligands, and the xi approximately t-regime by the kinetics of ligands-receptors association.

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Selected References

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  1. Albersdörfer A., Feder T., Sackmann E. Adhesion-induced domain formation by interplay of long-range repulsion and short-range attraction force: a model membrane study. Biophys J. 1997 Jul;73(1):245–257. doi: 10.1016/S0006-3495(97)78065-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bell G. I. Models for the specific adhesion of cells to cells. Science. 1978 May 12;200(4342):618–627. doi: 10.1126/science.347575. [DOI] [PubMed] [Google Scholar]
  3. Bruinsma R., Behrisch A., Sackmann E. Adhesive switching of membranes: experiment and theory. Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics. 2000 Apr;61(4 Pt B):4253–4267. doi: 10.1103/physreve.61.4253. [DOI] [PubMed] [Google Scholar]
  4. Dustin M. L., Ferguson L. M., Chan P. Y., Springer T. A., Golan D. E. Visualization of CD2 interaction with LFA-3 and determination of the two-dimensional dissociation constant for adhesion receptors in a contact area. J Cell Biol. 1996 Feb;132(3):465–474. doi: 10.1083/jcb.132.3.465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hu B., Finsinger D., Peter K., Guttenberg Z., Bärmann M., Kessler H., Escherich A., Moroder L., Böhm J., Baumeister W. Intervesicle cross-linking with integrin alpha IIb beta 3 and cyclic-RGD-lipopeptide. A model of cell-adhesion processes. Biochemistry. 2000 Oct 10;39(40):12284–12294. doi: 10.1021/bi000144q. [DOI] [PubMed] [Google Scholar]
  6. Huber W., Hurst J., Schlatter D., Barner R., Hübscher J., Kouns W. C., Steiner B. Determination of kinetic constants for the interaction between the platelet glycoprotein IIb-IIIa and fibrinogen by means of surface plasmon resonance. Eur J Biochem. 1995 Feb 1;227(3):647–656. doi: 10.1111/j.1432-1033.1995.tb20184.x. [DOI] [PubMed] [Google Scholar]
  7. Hynes R. O. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992 Apr 3;69(1):11–25. doi: 10.1016/0092-8674(92)90115-s. [DOI] [PubMed] [Google Scholar]
  8. Park K., Mao F. W., Park H. Morphological characterization of surface-induced platelet activation. Biomaterials. 1990 Jan;11(1):24–31. doi: 10.1016/0142-9612(90)90047-t. [DOI] [PubMed] [Google Scholar]
  9. Seifert U. Adhesion of vesicles in two dimensions. Phys Rev A. 1991 Jun 15;43(12):6803–6814. doi: 10.1103/physreva.43.6803. [DOI] [PubMed] [Google Scholar]
  10. Seifert U, Lipowsky R. Adhesion of vesicles. Phys Rev A. 1990 Oct 15;42(8):4768–4771. doi: 10.1103/physreva.42.4768. [DOI] [PubMed] [Google Scholar]
  11. Smilenov L. B., Mikhailov A., Pelham R. J., Marcantonio E. E., Gundersen G. G. Focal adhesion motility revealed in stationary fibroblasts. Science. 1999 Nov 5;286(5442):1172–1174. doi: 10.1126/science.286.5442.1172. [DOI] [PubMed] [Google Scholar]
  12. Toole B. P. Hyaluronan and its binding proteins, the hyaladherins. Curr Opin Cell Biol. 1990 Oct;2(5):839–844. doi: 10.1016/0955-0674(90)90081-o. [DOI] [PubMed] [Google Scholar]

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