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Pregled bibliografske jedinice broj: 262038

Antagonist-induced deadhesion of specically adhered vesicles


Smith, Ana-Sunčana; Lorz, Barbara; Seifert, Udo; Sackmann, Erich
Antagonist-induced deadhesion of specically adhered vesicles // Biophysical Journal, 90 (2006), 3; 1064-1080 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 262038 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Antagonist-induced deadhesion of specically adhered vesicles

Autori
Smith, Ana-Sunčana ; Lorz, Barbara ; Seifert, Udo ; Sackmann, Erich

Izvornik
Biophysical Journal (0006-3495) 90 (2006), 3; 1064-1080

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Cell-Adhesion; L-Selectin; Membrane; Ligand; Repulsion; Integrin; Cytoskeleton; Neutrophils; Transition; Microscopy

Sažetak
By use of a model system consisting of giant vesicles adhering to. at substrates, we identified, both experimentally and theoretically, two new control mechanisms for antagonist-induced deadhesion. Adhesion is established by specific binding of surface-grafted E-selectin and vesicle-carrying oligosaccharide Lewis(X). Deadhesion is achieved by controlled titration of monoclonal antibodies against E-selectin. The first mechanism is characterized by a considerable retraction of the contact zone resulting in a loss of contact area between the vesicle and the substrate. Within the developed theoretical framework, the observed equilibrium state is understood as a balance between the spreading pressure of the vesicle and the antagonist-induced lateral pressure at the edge of the contact zone. In the second mechanism, the antibodies induce unbinding by penetrating the contact zone without significantly affecting its size. This process reveals the decomposition of the adhesion zone into microdomains of tight binding separated by strongly fluctuating sections of the membrane. Both experiment and theory show a sigmoidal decrease of the number of bound ligands as a function of the logarithm of antagonist concentration. The work presented herein also provides a new method for the determination of the receptor binding affinity of either the surface-embedded ligands or the competing antagonist molecules.

Izvorni jezik
Engleski

Znanstvena područja
Fizika



POVEZANOST RADA


Ustanove:
Akademija likovnih umjetnosti, Zagreb

Profili:

Avatar Url Ana Sunčana Smith (autor)


Citiraj ovu publikaciju:

Smith, Ana-Sunčana; Lorz, Barbara; Seifert, Udo; Sackmann, Erich
Antagonist-induced deadhesion of specically adhered vesicles // Biophysical Journal, 90 (2006), 3; 1064-1080 (međunarodna recenzija, članak, znanstveni)
Smith, A., Lorz, B., Seifert, U. & Sackmann, E. (2006) Antagonist-induced deadhesion of specically adhered vesicles. Biophysical Journal, 90 (3), 1064-1080.
@article{article, author = {Smith, Ana-Sun\v{c}ana and Lorz, Barbara and Seifert, Udo and Sackmann, Erich}, year = {2006}, pages = {1064-1080}, keywords = {Cell-Adhesion, L-Selectin, Membrane, Ligand, Repulsion, Integrin, Cytoskeleton, Neutrophils, Transition, Microscopy}, journal = {Biophysical Journal}, volume = {90}, number = {3}, issn = {0006-3495}, title = {Antagonist-induced deadhesion of specically adhered vesicles}, keyword = {Cell-Adhesion, L-Selectin, Membrane, Ligand, Repulsion, Integrin, Cytoskeleton, Neutrophils, Transition, Microscopy} }
@article{article, author = {Smith, Ana-Sun\v{c}ana and Lorz, Barbara and Seifert, Udo and Sackmann, Erich}, year = {2006}, pages = {1064-1080}, keywords = {Cell-Adhesion, L-Selectin, Membrane, Ligand, Repulsion, Integrin, Cytoskeleton, Neutrophils, Transition, Microscopy}, journal = {Biophysical Journal}, volume = {90}, number = {3}, issn = {0006-3495}, title = {Antagonist-induced deadhesion of specically adhered vesicles}, keyword = {Cell-Adhesion, L-Selectin, Membrane, Ligand, Repulsion, Integrin, Cytoskeleton, Neutrophils, Transition, Microscopy} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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