Hud N V, Sklenár V, Feigon J
Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California, Los Angeles, 405 Hilgard Ave., Los Angeles, CA, 90095-1569, USA.
J Mol Biol. 1999 Feb 26;286(3):651-60. doi: 10.1006/jmbi.1998.2513.
Monovalent cation binding sites on nucleic acids in solution can be localized using the isotopically labeled ammonium ion (15NH4+) as a probe in high resolution NMR spectroscopy experiments. The application of this technique to a series of DNA duplexes reveals a preference for the binding of ammonium cations in the minor groove of A-tract sequences. These results are consistent with a recent report which indicates that some solvent electron densities previously identified as water molecules in DNA X-ray crystal structures are partially occupied by sodium ions. The sequence-specific nature of monovalent cation binding sites demonstrated here for A-tract DNA provides an explanation for the origin of sequence-directed bending.
溶液中核酸上的单价阳离子结合位点可以通过在高分辨率核磁共振光谱实验中使用同位素标记的铵离子(15NH4+)作为探针来定位。将该技术应用于一系列DNA双链体,结果表明铵阳离子更倾向于结合在A序列的小沟中。这些结果与最近的一份报告一致,该报告指出,DNA X射线晶体结构中一些先前被确定为水分子的溶剂电子密度部分被钠离子占据。此处展示的A序列DNA单价阳离子结合位点的序列特异性性质,为序列导向弯曲的起源提供了解释。