Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding
- Autores
- Iturri, Jagoba; García Fernández, Luis; Reuning, Ute; García, Andrés J.; del Campo, Aránzazu; Salierno, Marcelo Javier
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The Quartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify integrin-RGD recognition during the early stages of cell adhesion. Using QCM-D crystals modified with a photo-activatable RGD peptide, the time point of presentation of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled. This allowed temporal resolution of early integrin-RGD binding and the subsequent cell spreading process, and their separate detection by QCM-D. The specificity of the integrin-RGD binding event was corroborated by performing the experiments in the presence of soluble cyclicRGD as a competitor, and cytochalasin D as inhibitor of cell spreading. Larger frequency change in the QCM-D signal was observed for cells with larger spread area, and for cells overexpressing integrin avb3 upon stable transfection. This strategy enables quantification of integrin activity which, in turn, may allow discrimination among different cell types displaying distinct integrin subtypes and expression levels thereof. On the basis of these findings, we believe the strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as other several pathologies.
Fil: Iturri, Jagoba. Max Planck Institute for Polymer Research; Alemania
Fil: García Fernández, Luis. Max Planck Institute for Polymer Research; Alemania
Fil: Reuning, Ute. Technische Universitat Munchen; Alemania
Fil: García, Andrés J.. Georgia Institute Of Techology; Estados Unidos
Fil: del Campo, Aránzazu. Max Planck Institute for Polymer Research; Alemania
Fil: Salierno, Marcelo Javier. Max Planck Institute for Polymer Research; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
Integrins
Cancer screening
Lab-on-a-chip
Cell adhesion
QCM-D - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/16694
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Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin bindingIturri, JagobaGarcía Fernández, LuisReuning, UteGarcía, Andrés J.del Campo, AránzazuSalierno, Marcelo JavierIntegrinsCancer screeningLab-on-a-chipCell adhesionQCM-Dhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The Quartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify integrin-RGD recognition during the early stages of cell adhesion. Using QCM-D crystals modified with a photo-activatable RGD peptide, the time point of presentation of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled. This allowed temporal resolution of early integrin-RGD binding and the subsequent cell spreading process, and their separate detection by QCM-D. The specificity of the integrin-RGD binding event was corroborated by performing the experiments in the presence of soluble cyclicRGD as a competitor, and cytochalasin D as inhibitor of cell spreading. Larger frequency change in the QCM-D signal was observed for cells with larger spread area, and for cells overexpressing integrin avb3 upon stable transfection. This strategy enables quantification of integrin activity which, in turn, may allow discrimination among different cell types displaying distinct integrin subtypes and expression levels thereof. On the basis of these findings, we believe the strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as other several pathologies.Fil: Iturri, Jagoba. Max Planck Institute for Polymer Research; AlemaniaFil: García Fernández, Luis. Max Planck Institute for Polymer Research; AlemaniaFil: Reuning, Ute. Technische Universitat Munchen; AlemaniaFil: García, Andrés J.. Georgia Institute Of Techology; Estados UnidosFil: del Campo, Aránzazu. Max Planck Institute for Polymer Research; AlemaniaFil: Salierno, Marcelo Javier. Max Planck Institute for Polymer Research; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaNature Publishing Group2015-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/16694Iturri, Jagoba; García Fernández, Luis; Reuning, Ute; García, Andrés J.; del Campo, Aránzazu; et al.; Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding; Nature Publishing Group; Scientific Reports; 5; 3-2015; 1-8; 95332045-2322enginfo:eu-repo/semantics/altIdentifier/doi/10.1038/srep09533info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/srep09533info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379501/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:37:30Zoai:ri.conicet.gov.ar:11336/16694instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:37:31.104CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
title |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
spellingShingle |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding Iturri, Jagoba Integrins Cancer screening Lab-on-a-chip Cell adhesion QCM-D |
title_short |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
title_full |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
title_fullStr |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
title_full_unstemmed |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
title_sort |
Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding |
dc.creator.none.fl_str_mv |
Iturri, Jagoba García Fernández, Luis Reuning, Ute García, Andrés J. del Campo, Aránzazu Salierno, Marcelo Javier |
author |
Iturri, Jagoba |
author_facet |
Iturri, Jagoba García Fernández, Luis Reuning, Ute García, Andrés J. del Campo, Aránzazu Salierno, Marcelo Javier |
author_role |
author |
author2 |
García Fernández, Luis Reuning, Ute García, Andrés J. del Campo, Aránzazu Salierno, Marcelo Javier |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Integrins Cancer screening Lab-on-a-chip Cell adhesion QCM-D |
topic |
Integrins Cancer screening Lab-on-a-chip Cell adhesion QCM-D |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The Quartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify integrin-RGD recognition during the early stages of cell adhesion. Using QCM-D crystals modified with a photo-activatable RGD peptide, the time point of presentation of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled. This allowed temporal resolution of early integrin-RGD binding and the subsequent cell spreading process, and their separate detection by QCM-D. The specificity of the integrin-RGD binding event was corroborated by performing the experiments in the presence of soluble cyclicRGD as a competitor, and cytochalasin D as inhibitor of cell spreading. Larger frequency change in the QCM-D signal was observed for cells with larger spread area, and for cells overexpressing integrin avb3 upon stable transfection. This strategy enables quantification of integrin activity which, in turn, may allow discrimination among different cell types displaying distinct integrin subtypes and expression levels thereof. On the basis of these findings, we believe the strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as other several pathologies. Fil: Iturri, Jagoba. Max Planck Institute for Polymer Research; Alemania Fil: García Fernández, Luis. Max Planck Institute for Polymer Research; Alemania Fil: Reuning, Ute. Technische Universitat Munchen; Alemania Fil: García, Andrés J.. Georgia Institute Of Techology; Estados Unidos Fil: del Campo, Aránzazu. Max Planck Institute for Polymer Research; Alemania Fil: Salierno, Marcelo Javier. Max Planck Institute for Polymer Research; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
description |
The Quartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify integrin-RGD recognition during the early stages of cell adhesion. Using QCM-D crystals modified with a photo-activatable RGD peptide, the time point of presentation of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled. This allowed temporal resolution of early integrin-RGD binding and the subsequent cell spreading process, and their separate detection by QCM-D. The specificity of the integrin-RGD binding event was corroborated by performing the experiments in the presence of soluble cyclicRGD as a competitor, and cytochalasin D as inhibitor of cell spreading. Larger frequency change in the QCM-D signal was observed for cells with larger spread area, and for cells overexpressing integrin avb3 upon stable transfection. This strategy enables quantification of integrin activity which, in turn, may allow discrimination among different cell types displaying distinct integrin subtypes and expression levels thereof. On the basis of these findings, we believe the strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as other several pathologies. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-03 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/16694 Iturri, Jagoba; García Fernández, Luis; Reuning, Ute; García, Andrés J.; del Campo, Aránzazu; et al.; Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding; Nature Publishing Group; Scientific Reports; 5; 3-2015; 1-8; 9533 2045-2322 |
url |
http://hdl.handle.net/11336/16694 |
identifier_str_mv |
Iturri, Jagoba; García Fernández, Luis; Reuning, Ute; García, Andrés J.; del Campo, Aránzazu; et al.; Synchronized cell attachment triggered by photo-activatable adhesive ligands allows QCM-based detection of early integrin binding; Nature Publishing Group; Scientific Reports; 5; 3-2015; 1-8; 9533 2045-2322 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1038/srep09533 info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/srep09533 info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379501/ |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
publisher.none.fl_str_mv |
Nature Publishing Group |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846083495938490368 |
score |
12.891075 |