| Literature DB >> 17150733 |
Gosuke Hayashi1, Masaki Hagihara, Kazuhiko Nakatani.
Abstract
Enantiomeric DNA termed as L-DNA has unique properties. One is the ability of hybridizing to the complementary DNA as natural D-DNA. Another property is that the L-DNA could be recognized much more weakly by enzymes than D-DNA. We have focused our attention on these properties and applied L-DNA as a molecular tag. Here, we report that L-D chimera DNA is useful for PCR primers and subsequent separation and hybridization. Precise investigation revealed that in the process of PCR, L-DNA region could not be the PCR template and the polymerase extension reaction stopped at the boundary between L- and D-DNA region. As a result, L-DNA region formed like a "sticky end" and played a role of molecular tag. According to the L-DNA tag sequence, the produced L-DNA-tagged PCR products were easily separated or hybridized on the solid surface where the complementary L-DNA was pre-immobilized.Mesh:
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Year: 2005 PMID: 17150733 DOI: 10.1093/nass/49.1.261
Source DB: PubMed Journal: Nucleic Acids Symp Ser (Oxf) ISSN: 0261-3166