Published online 7 July 2005
Methods Online |
DNA microarrays on nanoscale-controlled surface
Department of Chemistry, Center for Integrated Molecular Systems, Division of Molecular and Life Sciences, Pohang University of Science and Technology Pohang 790-784, Korea
*To whom correspondence should be addressed. Tel: +82 54 279 2119; Fax: +82 54 279 0653; Email: jwpark{at}postech.ac.kr
Received April 24, 2005. Revised June 21, 2005. Accepted June 21, 2005.
We have developed new surface to ensure a proper spacing between immobilized biomolecules. While DNA microarray on this surface provided each probe DNA with ample space for hybridization with incoming target DNAs, the microarray showed enhanced discrimination efficiency for various types of single nucleotide polymorphism. The high discrimination efficiency holds for all tested cases (100:<1 for internal mismatched cases; 100:<28 for terminal mismatched ones). In addition, by investigating influence of hybridization temperature and washing condition on the fluorescence intensity and the discrimination efficiency with and without controlled mesospacing, it was observed that the nanoscale-controlled surface showed good discrimination efficiency in a wide range of temperature (3750°C), and hybridization behavior on the surface was in agreement with the solution one. Intriguingly, it was found that washing process after the hybridization was critical for the high discrimination efficiency. For the particular case, washing process was so efficient that only 30 s washing was sufficient to reach the optimal discrimination ratio.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
L. Poulsen, M. J. Soe, D. Snakenborg, L. B. Moller, and M. Dufva Multi-stringency wash of partially hybridized 60-mer probes reveals that the stringency along the probe decreases with distance from the microarray surface Nucleic Acids Res., November 1, 2008; 36(20): e132 - e132. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Pasternak, E. Kierzek, K. Pasternak, D. H. Turner, and R. Kierzek A chemical synthesis of LNA-2,6-diaminopurine riboside, and the influence of 2'-O-methyl-2,6-diaminopurine and LNA-2,6-diaminopurine ribosides on the thermodynamic properties of 2'-O-methyl RNA/RNA heteroduplexes Nucleic Acids Res., June 12, 2007; (2007) gkm421v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. E. Pozhitkov, R. D. Stedtfeld, S. A. Hashsham, and P. A. Noble Revision of the nonequilibrium thermal dissociation and stringent washing approaches for identification of mixed nucleic acid targets by microarrays Nucleic Acids Res., May 14, 2007; 35(9): e70 - e70. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Cattaruzza, A. Cricenti, A. Flamini, M. Girasole, G. Longo, T. Prosperi, G. Andreano, L. Cellai, and E. Chirivino Controlled loading of oligodeoxyribonucleotide monolayers onto unoxidized crystalline silicon; fluorescence-based determination of the surface coverage and of the hybridization efficiency; parallel imaging of the process by Atomic Force Microscopy Nucleic Acids Res., February 28, 2006; 34(4): e32 - e32. [Abstract] [Full Text] [PDF] |
||||
