Summary information and primary citation
- PDB-id
-
6rio;
DSSR-derived features in text and
JSON formats
- Class
- DNA
- Method
- NMR
- Summary
- Imidazole polyamide-DNA complex NMR structure
(5'-cgatgtacatcg-3')
- Reference
-
Padroni G, Withers JM, Taladriz-Sender A, Reichenbach LF,
Parkinson JA, Burley GA (2019): "Sequence-Selective
Minor Groove Recognition of a DNA Duplex Containing
Synthetic Genetic Components."
J.Am.Chem.Soc., 141, 9555-9563.
doi: 10.1021/jacs.8b12444.
- Abstract
- The structural basis of minor groove recognition of a
DNA duplex containing synthetic genetic information by
hairpin pyrrole-imidazole polyamides is described. Hairpin
polyamides induce a higher melting stabilization of a DNA
duplex containing the unnatural P·Z base-pair when an
imidazole unit is aligned with a P nucleotide. An NMR
structural study showed that the incorporation of two
isolated P·Z pairs enlarges the minor groove and slightly
narrows the major groove at the site of this synthetic
genetic information, relative to a DNA duplex consisting
entirely of Watson-Crick base-pairs. Pyrrole-imidazole
polyamides bind to a P·Z-containing DNA duplex to form a
stable complex, effectively mimicking a G·C pair. A
structural hallmark of minor groove recognition of a P·Z
pair by a polyamide is the reduced level of allosteric
distortion induced by binding of a polyamide to a DNA
duplex. Understanding the molecular determinants that
influence minor groove recognition of DNA containing
synthetic genetic components provides the basis to further
develop unnatural base-pairs for synthetic biology
applications.