Literature DB >> 17150733

Application of L-DNA as a molecular tag.

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.

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Substances:

Year:  2005        PMID: 17150733     DOI: 10.1093/nass/49.1.261

Source DB:  PubMed          Journal:  Nucleic Acids Symp Ser (Oxf)        ISSN: 0261-3166


  2 in total

Review 1.  Rational vector design for efficient non-viral gene delivery: challenges facing the use of plasmid DNA.

Authors:  Juergen Mairhofer; Reingard Grabherr
Journal:  Mol Biotechnol       Date:  2008-06       Impact factor: 2.695

2.  Utilising the left-helical conformation of L-DNA for analysing different marker types on a single universal microarray platform.

Authors:  Nicole C Hauser; Rafael Martinez; Anette Jacob; Steffen Rupp; Jörg D Hoheisel; Stefan Matysiak
Journal:  Nucleic Acids Res       Date:  2006-09-20       Impact factor: 16.971

  2 in total

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