Modulating surface density of proteins via caged surfaces and controlled light exposure

We demonstrate the possibility of tuning the degree of functionalization of a surface using photoactivatable chemistries and controlled light exposure. A photosensitive organosilane with a protected amine terminal group and a tetraethyleneglycol spacer was synthesized. A o-nitrobenzyl cage was used...

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Autor principal: Álvarez, M.
Otros Autores: Alonso, J.M, Filevich, O., Bhagawati, M., Etchenique, R., Piehler, J., Del Campo, A.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2011
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a protein, 67254-75-5; Photosensitizing Agents; Proteins 
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100 1 |a Álvarez, M. 
245 1 0 |a Modulating surface density of proteins via caged surfaces and controlled light exposure 
260 |c 2011 
270 1 0 |m Del Campo, A.; Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany; email: delcampo@mpip-mainz.mpg.de 
506 |2 openaire  |e Política editorial 
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520 3 |a We demonstrate the possibility of tuning the degree of functionalization of a surface using photoactivatable chemistries and controlled light exposure. A photosensitive organosilane with a protected amine terminal group and a tetraethyleneglycol spacer was synthesized. A o-nitrobenzyl cage was used as the photoremovable group to cage the amine functionality. Surfaces with phototunable amine densities were generated by controlled irradiation of silica substrates modified with the photosensitive anchor. Protein layers with different densities could be obtained by successive coupling and assembly steps. Protein surface concentrations were quantified by reflectance interference. Our results demonstrate that the protein density correlates with the photogenerated ligand density. The density control was proved over four coupling steps (biotin, SAv, BTtris-NTA, MBP, or GFP), indicating that the interactions between underlying layer and soluble targets are highly specific and the immobilized targets at the four levels maintain their full functionality. Protein micropatterns with a gradient of protein density were also obtained. © 2011 American Chemical Society.  |l eng 
593 |a Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany 
593 |a Max Planck Institut für Metallforschung, Heisenbergstrasse 3, 70569 Stuttgart, Germany 
593 |a Departamento de Quimica Inorganica, Analitica y Quimica Fisica, INQUIMAE, Universidad de Buenos Aires, Ciudad Universitaria Pabellón 2 Piso 3, C1428EHA, Buenos Aires, Argentina 
593 |a Universität Osnabrück, Barbarastrasse 11, 49076 Osnabrück, Germany 
593 |a CIC NanoGUNE Consolider, Tolosa Hiribidea, 76, 20018 San Sebastián, Spain 
690 1 0 |a AMINE FUNCTIONALITY 
690 1 0 |a DEGREE OF FUNCTIONALIZATION 
690 1 0 |a DENSITY CONTROL 
690 1 0 |a LIGAND DENSITY 
690 1 0 |a LIGHT EXPOSURE 
690 1 0 |a ORGANOSILANES 
690 1 0 |a PHOTO-TUNABLE 
690 1 0 |a PHOTOACTIVATABLE 
690 1 0 |a PROTEIN DENSITY 
690 1 0 |a PROTEIN LAYERS 
690 1 0 |a PROTEIN MICROPATTERNS 
690 1 0 |a PROTEIN SURFACE 
690 1 0 |a SILICA SUBSTRATE 
690 1 0 |a SURFACE DENSITY 
690 1 0 |a TERMINAL GROUPS 
690 1 0 |a UNDERLYING LAYERS 
690 1 0 |a LIGHT SENSITIVE MATERIALS 
690 1 0 |a ORGANIC COMPOUNDS 
690 1 0 |a PHOTOSENSITIVITY 
690 1 0 |a SILICA 
690 1 0 |a PROTEINS 
690 1 0 |a PHOTOSENSITIZING AGENT 
690 1 0 |a PROTEIN 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMISTRY 
690 1 0 |a LIGHT 
690 1 0 |a PHOTOCHEMISTRY 
690 1 0 |a SURFACE PROPERTY 
690 1 0 |a SYNTHESIS 
690 1 0 |a LIGHT 
690 1 0 |a PHOTOCHEMICAL PROCESSES 
690 1 0 |a PHOTOSENSITIZING AGENTS 
690 1 0 |a PROTEINS 
690 1 0 |a SURFACE PROPERTIES 
700 1 |a Alonso, J.M. 
700 1 |a Filevich, O. 
700 1 |a Bhagawati, M. 
700 1 |a Etchenique, R. 
700 1 |a Piehler, J. 
700 1 |a Del Campo, A. 
773 0 |d 2011  |g v. 27  |h pp. 2789-2795  |k n. 6  |p Langmuir  |x 07437463  |t Langmuir 
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