Nucleic Acids Research Advance Access originally published online on February 13, 2008
Nucleic Acids Research 2008 36(6):1952-1964; doi:10.1093/nar/gkm927
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Nucleic Acids Research, 2008, Vol. 36, No. 6 1952-1964
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Chemistry |
‘Protected DNA Probes’ capable of strong hybridization without removal of base protecting groups
1Department of Life Science, Tokyo Institute of Technology, 4259 Nagatsuta, Midoriku, Yokohama 226-8501, Japan, 2CREST, JST (Japan Science and Technology Agency), 4-1-8 Honcho, Kawaguchi 332-0012, 3New Product Development Department, Sonac Incorporated, 1-5-1 Nishishinbashi, Minato-ku, Tokyo 105-0003, 4Center for Nano Materials and Technology, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Tatsunokuchi, Ishikawa 923-1292 and 5Genosys Division, Sigma-Aldrich Japan, Ishikari 061-3241, Japan
*To whom correspondence should be addressed. Tel: +81 45 924 5706; Fax: +81 45 924 5772; Email: msekine{at}bio.titech.ac.jp
Received September 6, 2007. Revised October 9, 2007. Accepted October 10, 2007.
We propose a new strategy called the ‘Protected DNA Probes (PDP) method’ in which appropriately protected bases selectively bind to the complementary bases without the removal of their base protecting groups. Previously, we reported that 4-N-acetylcytosine oligonucleotides (ac4C) exhibited a higher hybridization affinity for ssDNA than the unmodified oligonucleotides. For the PDP strategy, we created a modified adenine base and synthesized an N-acylated deoxyadenosine mimic having 6-N-acetyl-8-aza-7-deazaadenine (ac6az8c7A). It was found that PDP containing ac4C and ac6az8c7A exhibited higher affinity for the complementary ssDNA than the corresponding unmodified DNA probes and showed similar base recognition ability. Moreover, it should be noted that this PDP strategy could guarantee highly efficient synthesis of DNA probes on controlled pore glass (CPG) with high purity and thereby could eliminate the time-consuming procedures for isolating DNA probes. This strategy could also avoid undesired base-mediated elimination of DNA probes from CPG under basic conditions such as concentrated ammonia solution prescribed for removal of base protecting groups in the previous standard approach. Here, several successful applications of this strategy to single nucleotide polymorphism detection are also described in detail using PDPs immobilized on glass plates and those prepared on CPG plates, suggesting its potential usefulness.