Why does TNA cross-pair more strongly with RNA than with DNA? An answer from X-ray analysis

被引:59
作者
Pallan, PS
Wilds, CJ
Wawrzak, Z
Krishnamurthy, R
Eschenmoser, A
Egli, M [1 ]
机构
[1] Vanderbilt Univ, Dept Biochem, Nashville, TN 37332 USA
[2] Concordia Univ, Dept Chem & Biochem, Montreal, PQ H4B 1R6, Canada
[3] Argonne Natl Lab, DND CAT Synchrotron Res Ctr, Argonne, IL 60439 USA
[4] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[5] ETH, Lab Organ Chem, CH-8093 Zurich, Switzerland
关键词
conformation analysis; DNA; RNA; structure elucidation; TNA;
D O I
10.1002/anie.200352553
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The TNA twist: L-α-threofuranosyl (3′↔2′) nucleic acid (TNA) residues adopt a C4′-exo pucker when incorporated into an A-(left) or a B-form DNA duplex (right). The resulting intranucleotide P⋯P distance in TNA is very similar to that in RNA (represented by a C3′-endo puckered adenosine residue; green). The structural data explain earlier observations that TNA hydridizes more stably with RNA than with DNA and that RNA constitutes the better template for ligating TNA fragments.
引用
收藏
页码:5893 / 5895
页数:3
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