Gaynutdinov Timur I, Neumann Ronald D, Panyutin Igor G
Department of Nuclear Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Int J Radiat Biol. 2008 Dec;84(12):984-90. doi: 10.1080/09553000802415747.
A repeated, non-coding, DNA sequence d(TTAGGG)(n) is present in the telomeric ends of all human chromosomes. These repeats can adopt multiple inter- and intra-molecular non-B-DNA conformations that may play an important role in biological processes. We applied (125)I -radioprobing to assess the conformation of the human telomeric DNA fragment in a complex with the quadruplex-specific drug - cationic porphyrin TMPyP4.
Synthetic DNA oligonucleotides containing the telomeric sequence were labeled with (125)I. The probability of DNA breaks caused by decay of (125)I is inversely related to the distance between the radionuclide and the sugar unit of the DNA backbone; hence, the conformation of the DNA backbone can be deduced from the distribution of breaks.
The obtained data indicate that the telomeric oligonucleotides predominantly fold into an intramolecular quadruplex conformation in the presence of TMPyP4. We propose a mixed-type (3 + 1) conformation of telomeric quadruplex in a complex with the cationic porphyrin TMPyP4 in solution. Binding of the porphyrin overrides the counterion effect on quadruplex conformation.
We have demonstrated that (125)I radioprobing can be successfully applied not only to determine folding in G-quadruplexes, but also to reveal the mode of quadruplex interaction with small ligands.
重复的非编码DNA序列d(TTAGGG)(n)存在于所有人染色体的端粒末端。这些重复序列可呈现多种分子间和分子内的非B-DNA构象,可能在生物学过程中发挥重要作用。我们应用¹²⁵I放射性探测来评估人端粒DNA片段与四链体特异性药物——阳离子卟啉TMPyP4形成复合物时的构象。
含有端粒序列的合成DNA寡核苷酸用¹²⁵I进行标记。¹²⁵I衰变引起DNA断裂的概率与放射性核素和DNA主链糖单元之间的距离成反比;因此,可从断裂分布推断DNA主链的构象。
所得数据表明,在TMPyP4存在下,端粒寡核苷酸主要折叠成分子内四链体构象。我们提出溶液中与阳离子卟啉TMPyP4形成复合物的端粒四链体的混合型(3 + 1)构象。卟啉的结合克服了抗衡离子对四链体构象的影响。
我们已证明¹²⁵I放射性探测不仅可成功用于确定G-四链体中的折叠情况,还可揭示四链体与小配体的相互作用模式。