Synthesis of a Single G-Quartet Platform in Water

被引:21
作者
Bare, Grant A. L. [1 ]
Liu, Bo [1 ]
Sherman, John C. [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
G-QUADRUPLEX LIGAND; TELOMERIC DNA; PROTON-EXCHANGE; G-TETRAPLEX; MODEL; TRIAZATRUXENE; ASSOCIATION; DERIVATIVES; PORPHYRIN; COMPOUND;
D O I
10.1021/ja405100z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For over 50 years the G-quartet has been a defining self-assembled structure in biology and non-covalent synthesis. It is shown here for the first time that the G-quartet is isolatable in water in the absence of stabilizing G-quartet stacking or cations through the construction of a phosphate-linked template-assembled synthetic G-quartet. Synthetic design has facilitated preservation of the guanine base, ribose sugar, and phosphate components with correct linkage chemistry relative to G-quadruplex DNA. Thus, a minimal synthetic model of G-quadruplex DNA, as in that associated with human gene promoter or telomere regions, is represented by this system. An application as a probe for interactions between G-quadruplex DNA and potential anticancer therapeutical binding ligands is demonstrated. Binding constants of 10(5)-10(7) M-1 magnitude and 1:1 stoichiometries for TMPyP4, piper, and azatrux ligands were determined, whereas perturbations in BSU1051 and BRACO19 ligand signal were not observed. These data suggest a unique test for critical end-stacking interactions at the exclusion of intercalative or looping interactions for G-quadruplex binding ligands.
引用
收藏
页码:11985 / 11989
页数:5
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