Rahimian Maryam, Kumar Arvind, Say Martial, Bakunov Stanislav A, Boykin David W, Tidwell Richard R, Wilson W David
Department of Chemistry, Georgia State University, P.O. Box 4098, Atlanta, Georgia 30302, USA.
Biochemistry. 2009 Feb 24;48(7):1573-83. doi: 10.1021/bi801944g.
Most A/T specific heterocyclic diamidine derivatives need at least four A/T base pairs for tight binding to the DNA minor groove. Addition of a GC base pair to A/T sequences typically causes a large decrease in binding constant. The ability to target biologically important sequences of DNA could be significantly increased if compounds that could recognize A/T sites with an intervening GC base pair could be designed. The kinetoplast DNA sequence of parasitic microorganisms, for example, contains numerous three A/T binding sites that are separated by a single G. A series of compounds were prepared to target the AAAGTTT sequence as a model system for discovery of "G-jumpers". The new synthetic compounds have two aromatic-amidine groups for A/T recognition, and these are connected through an oxy-methylene linker to cross the GC. CD experiments indicated a minor groove binding mode, as expected, for these compounds. T(max), surface plasmon resonance, and isothermal titration calorimetry experiments revealed 1:1 binding to the AAAGTTT sequence with an affinity that depends on compound structure. Benzimidazole derivatives gave the strongest binding and had generally good solution properties. The binding affinities to the classical AATT sequence were similar to that for AAAGTTT for these extended compounds, but binding was weaker to the AAAGCTTT sequence with two intervening GC base pairs. Binding to both AAAGTTT and AATT was enthalpy driven for strong binding benzimidazole derivatives.
大多数A/T特异性杂环二脒衍生物需要至少四个A/T碱基对才能紧密结合到DNA小沟。在A/T序列中添加一个GC碱基对通常会导致结合常数大幅下降。如果能够设计出能够识别带有中间GC碱基对的A/T位点的化合物,那么靶向DNA生物学重要序列的能力可能会显著提高。例如,寄生微生物的动质体DNA序列包含许多由单个G隔开的三个A/T结合位点。制备了一系列化合物以靶向AAAGTTT序列,作为发现“G跳跃者”的模型系统。新的合成化合物具有两个用于识别A/T的芳基脒基团,它们通过氧亚甲基连接基相连以跨越GC。圆二色性实验表明,正如预期的那样,这些化合物具有小沟结合模式。T(max)、表面等离子体共振和等温滴定量热实验表明,这些化合物与AAAGTTT序列以1:1的比例结合,亲和力取决于化合物结构。苯并咪唑衍生物的结合力最强,并且通常具有良好的溶液性质。对于这些扩展化合物,它们与经典AATT序列的结合亲和力与与AAAGTTT序列的相似,但与带有两个中间GC碱基对的AAAGCTTT序列的结合较弱。对于强结合的苯并咪唑衍生物,与AAAGTTT和AATT的结合都是由焓驱动的。