Micro patterning of active proteins with perforated PDMS sheets (PDMS sieve)
- 6 April 2004
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Lab on a Chip
- Vol. 4 (4) , 333-336
- https://doi.org/10.1039/b400774c
Abstract
We propose a novel technique for patterning active proteins on a glass substrate using a perforated polydimethylsiloxane (PDMS) sheet–sieve. The sieve, which has tapering holes, is fabricated by spin-coating PDMS on a pyramidal-shaped mold. By means of this sieve, FITC (fluorescent isothiocyanate, bovine)–albumin was successfully spotted in a 5 × 5 µm2 area in an array. The patterned spots were perfectly isolated, which eliminates the problem of non-specific binding of proteins to undesired areas. To show that proteins maintained their activity after the patterning, we used F1-ATPase biomolecular motors; their activity can easily be verified by observing their rotary motion after patterning. Selective patterning with three kinds of fluorescent micro beads indicated the possibility of patterning of different proteins on the same substrate by using the sieve.Keywords
This publication has 13 references indexed in Scilit:
- Macro-/Nanoporous Silicon as a Support for High-Performance Protein MicroarraysAnalytical Chemistry, 2003
- Light Activated Patterning of Dye-Labeled Molecules on SurfacesJournal of the American Chemical Society, 2003
- Protein patterning on silicon-based surface using background hydrophobic thin filmBiosensors and Bioelectronics, 2002
- Global Analysis of Protein Activities Using Proteome ChipsScience, 2001
- Patterning proteins and cells using soft lithographyBiomaterials, 1999
- Electrospray Deposition as a Method for Mass Fabrication of Mono- and Multicomponent Microarrays of Biological and Biologically Active SubstancesAnalytical Chemistry, 1999
- Protein patterningBiomaterials, 1998
- Direct observation of the rotation of F1-ATPaseNature, 1997
- Fabrication of Submicrometer Features on Curved Substrates by Microcontact PrintingScience, 1995
- A novel method for the parallel analysis of multiple mutations in multiple samplesNucleic Acids Research, 1993