Phan Anh Tuân, Kuryavyi Vitaly, Luu Kim Ngoc, Patel Dinshaw J
Structural Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Nucleic Acids Res. 2007;35(19):6517-25. doi: 10.1093/nar/gkm706. Epub 2007 Sep 25.
Intramolecular G-quadruplexes formed by human telomere sequences are attractive anticancer targets. Recently, four-repeat human telomere sequences have been shown to form two different intramolecular (3 + 1) G-quadruplexes in K(+) solution (Form 1 and Form 2). Here we report on the solution structures of both Form 1 and Form 2 adopted by natural human telomere sequences. Both structures contain the (3 + 1) G-tetrad core with one double-chain-reversal and two edgewise loops, but differ in the successive order of loop arrangements within the G-quadruplex scaffold. Our results provide the structural details at the two ends of the G-tetrad core in the context of natural sequences and information on different loop conformations. This structural information might be important for our understanding of telomere G-quadruplex structures and for anticancer drug design targeted to such scaffolds.
由人类端粒序列形成的分子内G-四链体是具有吸引力的抗癌靶点。最近,已证明四重复人类端粒序列在K(+)溶液中可形成两种不同的分子内(3 + 1) G-四链体(形式1和形式2)。在此,我们报道天然人类端粒序列所采用的形式1和形式2的溶液结构。两种结构均包含具有一个双链反转和两个边缘环的(3 + 1) G-四联体核心,但在G-四链体支架内的环排列连续顺序上有所不同。我们的结果提供了天然序列背景下G-四联体核心两端的结构细节以及不同环构象的信息。这些结构信息对于我们理解端粒G-四链体结构以及针对此类支架的抗癌药物设计可能很重要。