O Bornet, G Lancelot, L Chanteloup, T T Nguyen, J M Beau
Index: J. Biomol. NMR 4(4) , 575-80, (1994)
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We present NMR studies of an intramolecular triple helix, the three strands of which have been linked by a hexaethylene glycol chain. To overcome the generally encountered difficulties of assignment in the homo-pyrimidine strands, the carbon Cl' of the pyrimidines were selectively 13C-enriched. Assignments of the aromatic and sugar protons were obtained from NOESY-HMQC and TOCSY-HMQC spectra. We show that the recognition of a DNA duplex by a third strand via triplex formation is easily carried out in solution by observing the changes of the 1Hl'-13Cl' connectivities as a function of pH. Furthermore, the conformation of the sugars has been found to be C2'-endo, on the basis of the coupling constant values directly measured in an HSQC spectrum.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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hexaethyleneglycol
CAS:2615-15-8 |
C12H26O7 |
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