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1X6W

Solution Structure of the DNA Duplex TGCGCA:TGCGCA Capped by Trimethoxystilbene Residues

Summary for 1X6W
Entry DOI10.2210/pdb1x6w/pdb
Descriptor5'-D(*(TMS)P*TP*GP*CP*GP*CP*A)-3' (1 entity in total)
Functional Keywordsdna, trimethoxystilbene, synthetic hybrid
Total number of polymer chains2
Total formula weight4325.26
Authors
Tuma, J.,Paulini, R.,Sttz, J.,Richert, C. (deposition date: 2004-08-12, release date: 2004-10-05, Last modification date: 2024-05-22)
Primary citationTuma, J.,Paulini, R.,Rojas Stutz, J.A.,Richert, C.
How much pi-stacking do DNA termini seek? Solution structure of a self-complementary DNA hexamer with trimethoxystilbenes capping the terminal base pairs.
Biochemistry, 43:15680-15687, 2004
Cited by
PubMed Abstract: The exposed terminal base pairs of DNA duplexes are nonclassical binding sites for small molecules. Instead, small molecules usually prefer intercalation or minor groove binding. Here we report the solution structure of the DNA duplex (TMS-TGCGCA)(2), where TMS denotes trimethoxystilbene carboxamides that are 5'-tethered to the DNA. The stilbenes, for which intercalation is conformationally accessible, stack on the terminal T:A base pairs of an undisturbed B-form duplex. Two conformations, differing by the orientation of the stilbene relative to the terminal base pair, are observed, indicating that the flip rate is slow for the pi-stacked aromatic ring system. The trimethoxystilbene is known to greatly increase base pairing fidelity at the terminus. Here we show that it gauges the size of the T:A base pair by embracing the 2'-methylene group of the terminal dA residue of the unmodified terminus with its methoxy "arms", but that it does not engage the entire base pair in pi-stacking. Mismatched base pairs with their altered geometry will not allow for the same embracing interaction. On the basis of the current structure, a trimethoxychrysene carboxamide is proposed as a ligand with increased pi-stacking surface and possible applications as improved fidelity-enhancing element.
PubMed: 15595824
DOI: 10.1021/bi048205y
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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