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Photocleavable linker for the patterning of bioactive molecules

Herein, we report the use of a versatile photocleavable nitrobenzyl linker to micropattern a wide variety of bioactive molecules and photorelease them on demand. On one end, the linker has an NHS group that can be coupled with any amine, such as peptides, proteins or amine-linkers, and on the other...

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Autores principales: Wegner, Seraphine V., Sentürk, Oya I., Spatz, Joachim P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680943/
https://www.ncbi.nlm.nih.gov/pubmed/26670693
http://dx.doi.org/10.1038/srep18309
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author Wegner, Seraphine V.
Sentürk, Oya I.
Spatz, Joachim P.
author_facet Wegner, Seraphine V.
Sentürk, Oya I.
Spatz, Joachim P.
author_sort Wegner, Seraphine V.
collection PubMed
description Herein, we report the use of a versatile photocleavable nitrobenzyl linker to micropattern a wide variety of bioactive molecules and photorelease them on demand. On one end, the linker has an NHS group that can be coupled with any amine, such as peptides, proteins or amine-linkers, and on the other end an alkyne for convenient attachment to materials with an azide functional group. This linker was conjugated with NTA-amine or the cell adhesion peptide cRGD to enable straightforward patterning of His6-tagged proteins or cells, respectively, on PEGylated glass surfaces. This approach provides a practical way to control the presentation of a wide variety of bioactive molecules with high spatial and temporal resolution. The extent of photocleavage can also be controlled to tune the biomolecule density and degree of cell attachment to the surface.
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spelling pubmed-46809432015-12-18 Photocleavable linker for the patterning of bioactive molecules Wegner, Seraphine V. Sentürk, Oya I. Spatz, Joachim P. Sci Rep Article Herein, we report the use of a versatile photocleavable nitrobenzyl linker to micropattern a wide variety of bioactive molecules and photorelease them on demand. On one end, the linker has an NHS group that can be coupled with any amine, such as peptides, proteins or amine-linkers, and on the other end an alkyne for convenient attachment to materials with an azide functional group. This linker was conjugated with NTA-amine or the cell adhesion peptide cRGD to enable straightforward patterning of His6-tagged proteins or cells, respectively, on PEGylated glass surfaces. This approach provides a practical way to control the presentation of a wide variety of bioactive molecules with high spatial and temporal resolution. The extent of photocleavage can also be controlled to tune the biomolecule density and degree of cell attachment to the surface. Nature Publishing Group 2015-12-16 /pmc/articles/PMC4680943/ /pubmed/26670693 http://dx.doi.org/10.1038/srep18309 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wegner, Seraphine V.
Sentürk, Oya I.
Spatz, Joachim P.
Photocleavable linker for the patterning of bioactive molecules
title Photocleavable linker for the patterning of bioactive molecules
title_full Photocleavable linker for the patterning of bioactive molecules
title_fullStr Photocleavable linker for the patterning of bioactive molecules
title_full_unstemmed Photocleavable linker for the patterning of bioactive molecules
title_short Photocleavable linker for the patterning of bioactive molecules
title_sort photocleavable linker for the patterning of bioactive molecules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4680943/
https://www.ncbi.nlm.nih.gov/pubmed/26670693
http://dx.doi.org/10.1038/srep18309
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