Abstract
Traditionally, isotope-labelled DNA and RNA have been fundamental to nucleic acid structural studies by NMR. Four-stranded nucleic acid architectures studies increasingly benefit from a plethora of nucleotide conjugates for resonance assignments, the identification of hydrogen bond alignments, and improving the population of preferred species within equilibria. In this paper, we review their use for these purposes. Most importantly we identify reasons for the failure of some modifications to result in quadruplex formation.
| Original language | English |
|---|---|
| Pages (from-to) | 13073-13086 |
| Number of pages | 14 |
| Journal | Molecules |
| Volume | 17 |
| Issue number | 11 |
| Early online date | 5 Nov 2012 |
| DOIs | |
| Publication status | Published online - 5 Nov 2012 |
Keywords
- chemical modifications
- 8-bromoguanosine
- quadruplex
- 2,6-diaminopurine
- LNA
- inosine
- 8-O-methylguanine
- 8-methylguanine
- 5-bromouracil
- riboguanosine
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