Redesigning nucleic acids

A research program has applied the tools of synthetic organic chemistry to systematically modify the structure of DNA and RNA oligonucleotides to learn more about the chemical principles underlying their ability to store and transmit genetic information. Oligonucleotides (as opposed to nucleosides)...

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Veröffentlicht in:Pure and applied chemistry 1998-02, Vol.70 (2), p.263-266
Hauptverfasser: Benner, S. A., Battersby, T. R., Eschgfäller, Bernd, Hutter, Daniel, Kodra, J. T., Lutz, Stefan, Arslan, Tuncer, Bäschlin, D. K., Blättler, M., Egli, Martin, Hammer, Christophe, Held, H. A., Horlacher, Jennifer, Huang, Zh, Hyrup, Birgitte, Jenny, T. F., Jurczyk, S. C., König, H. A., von Krosigk, U., Lutz, M. J., MacPherson, L. J., Moroney, S. E., Müller, E., Nambiar, K. P., Piccirilli, J. A., Switzer, C. Y., Vögel, J. J., Richert, C., Roughton, A. L., Schmidt, J., Schneider, K. C., Stackhouse, J.
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Sprache:eng
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Zusammenfassung:A research program has applied the tools of synthetic organic chemistry to systematically modify the structure of DNA and RNA oligonucleotides to learn more about the chemical principles underlying their ability to store and transmit genetic information. Oligonucleotides (as opposed to nucleosides) have long been overlooked by synthetic organic chemists as targets for structural modification. Synthetic chemistry has now yielded oligonucleotides with 12 replicatable letters, modified backbones, and new insight into why Nature chose the oligonucleotide structures that she did.
ISSN:0033-4545
1365-3075
DOI:10.1351/pac199870020263