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Abstract:
As a part of our ongoing efforts to define the structural aspects of unusual pairing alignments in DNA triplexes by Nuclear Magnetic Resonance spectroscopy, we have examined the structural role of a nonnatural deoxyribonucleoside, P1, that has been shown to mediate the recognition of GC base pairs in pyrimidine-purine-pyrimidine DNA triplexes. A qualitative interpretation of the NMR data indicates that this analog of protonated cytosines is readily accommodated in the third strand segment of an intramolecular triplex system. Furthermore, the observed NOE patterns position the imino and amino protons of P1 opposite the Nitrate and Oxyide atome of guanine respectively, consistent with the previously proposed pairing scheme
| Limitations: |
 APPROVED FOR PUBLIC RELEASE |
| Description: |
Technical rept. |
| Pages: |
21 |
| Report Date: |
01 JUN 93 |
| Contract Number: |
N00014-92-J-1052 |
| Report Number: |
A215562 |
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