Cargando…

Protein patterning by microcontact printing using pyramidal PDMS stamps

Micro-contact printing, μCP, is a well-established soft-lithography technique for printing biomolecules. μCP uses stamps made of Poly(dimethylsiloxane), PDMS, made by replicating a microstructured silicon master fabricated by semiconductor manufacturing processes. One of the problems of the μCP is t...

Descripción completa

Detalles Bibliográficos
Autores principales: Filipponi, Luisa, Livingston, Peter, Kašpar, Ondřej, Tokárová, Viola, Nicolau, Dan V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718951/
https://www.ncbi.nlm.nih.gov/pubmed/26782964
http://dx.doi.org/10.1007/s10544-016-0036-4
_version_ 1782410863597060096
author Filipponi, Luisa
Livingston, Peter
Kašpar, Ondřej
Tokárová, Viola
Nicolau, Dan V.
author_facet Filipponi, Luisa
Livingston, Peter
Kašpar, Ondřej
Tokárová, Viola
Nicolau, Dan V.
author_sort Filipponi, Luisa
collection PubMed
description Micro-contact printing, μCP, is a well-established soft-lithography technique for printing biomolecules. μCP uses stamps made of Poly(dimethylsiloxane), PDMS, made by replicating a microstructured silicon master fabricated by semiconductor manufacturing processes. One of the problems of the μCP is the difficult control of the printing process, which, because of the high compressibility of PDMS, is very sensitive to minute changes in the applied pressure. This over-sensitive response leads to frequent and/or uncontrollable collapse of the stamps with high aspect ratios, thus decreasing the printing accuracy and reproducibility. Here we present a straightforward methodology of designing and fabricating PDMS structures with an architecture which uses the collapse of the stamp to reduce, rather than enlarge the variability of the printing. The PDMS stamp, organized as an array of pyramidal micro-posts, whose ceiling collapses when pressed on a flat surface, replicates the structure of the silicon master fabricated by anisotropic wet etching. Upon application of pressure, depending on the size of, and the pitch between, the PDMS pyramids, an air gap is formed surrounding either the entire array, or individual posts. The printing technology, which also exhibits a remarkably low background noise for fluorescence detection, may find applications when the clear demarcation of the shapes of protein patterns and the distance between them are critical, such as microarrays and studies of cell patterning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10544-016-0036-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4718951
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-47189512016-01-27 Protein patterning by microcontact printing using pyramidal PDMS stamps Filipponi, Luisa Livingston, Peter Kašpar, Ondřej Tokárová, Viola Nicolau, Dan V. Biomed Microdevices Article Micro-contact printing, μCP, is a well-established soft-lithography technique for printing biomolecules. μCP uses stamps made of Poly(dimethylsiloxane), PDMS, made by replicating a microstructured silicon master fabricated by semiconductor manufacturing processes. One of the problems of the μCP is the difficult control of the printing process, which, because of the high compressibility of PDMS, is very sensitive to minute changes in the applied pressure. This over-sensitive response leads to frequent and/or uncontrollable collapse of the stamps with high aspect ratios, thus decreasing the printing accuracy and reproducibility. Here we present a straightforward methodology of designing and fabricating PDMS structures with an architecture which uses the collapse of the stamp to reduce, rather than enlarge the variability of the printing. The PDMS stamp, organized as an array of pyramidal micro-posts, whose ceiling collapses when pressed on a flat surface, replicates the structure of the silicon master fabricated by anisotropic wet etching. Upon application of pressure, depending on the size of, and the pitch between, the PDMS pyramids, an air gap is formed surrounding either the entire array, or individual posts. The printing technology, which also exhibits a remarkably low background noise for fluorescence detection, may find applications when the clear demarcation of the shapes of protein patterns and the distance between them are critical, such as microarrays and studies of cell patterning. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10544-016-0036-4) contains supplementary material, which is available to authorized users. Springer US 2016-01-19 2016 /pmc/articles/PMC4718951/ /pubmed/26782964 http://dx.doi.org/10.1007/s10544-016-0036-4 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Filipponi, Luisa
Livingston, Peter
Kašpar, Ondřej
Tokárová, Viola
Nicolau, Dan V.
Protein patterning by microcontact printing using pyramidal PDMS stamps
title Protein patterning by microcontact printing using pyramidal PDMS stamps
title_full Protein patterning by microcontact printing using pyramidal PDMS stamps
title_fullStr Protein patterning by microcontact printing using pyramidal PDMS stamps
title_full_unstemmed Protein patterning by microcontact printing using pyramidal PDMS stamps
title_short Protein patterning by microcontact printing using pyramidal PDMS stamps
title_sort protein patterning by microcontact printing using pyramidal pdms stamps
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718951/
https://www.ncbi.nlm.nih.gov/pubmed/26782964
http://dx.doi.org/10.1007/s10544-016-0036-4
work_keys_str_mv AT filipponiluisa proteinpatterningbymicrocontactprintingusingpyramidalpdmsstamps
AT livingstonpeter proteinpatterningbymicrocontactprintingusingpyramidalpdmsstamps
AT kasparondrej proteinpatterningbymicrocontactprintingusingpyramidalpdmsstamps
AT tokarovaviola proteinpatterningbymicrocontactprintingusingpyramidalpdmsstamps
AT nicolaudanv proteinpatterningbymicrocontactprintingusingpyramidalpdmsstamps