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Pernilla Wittung (Institutionen för fysikalisk kemi) ; P. E. Nielsen ; O. Buchardt ; M. Egholm ; Bengt Nordén (Institutionen för fysikalisk kemi)
Nature (0028-0836). Vol. 368 (1994), 6471, p. 561-563.
[Artikel, refereegranskad vetenskaplig]

ALTHOUGH the importance of the nucleobases in the DNA double helix is well understood, the evolutionary significance of the deoxyribose phosphate backbone and the contribution of this chemical entity to the overall helical structure and stability of the double helix is not so clear. Peptide nucleic acid (PNA)1-7 is a DNA analogue with a backbone consisting of N-(2-aminoethyl)glycine units (Fig. 1) which has been shown to mimic DNA in forming Watson-Crick complementary duplexes with normal DNA7. Using circular dichroism spectroscopy we show here that two complementary PNA strands can hybridize to one another to form a helical duplex. There is a seeding of preferred chirality which is induced by the presence of an L- (or D-) lysine residue attached at the carboxy terminus of the PNA strand. These results indicate that a (deoxy)ribose phosphate backbone is not an essential requirement for the formation of double helical DNA-like structures in solution.

Nyckelord: recognition, thymine

Denna post skapades 2011-08-10. Senast ändrad 2017-11-29.
CPL Pubid: 144037


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