Nordell Pär, Westerlund Fredrik, Reymer Anna, El-Sagheer Afaf H, Brown Tom, Nordén Bengt, Lincoln Per
Department of Chemical and Biological Engineering, Chalmers University of Technology, SE-41296 Gothenburg, Sweden.
J Am Chem Soc. 2008 Nov 5;130(44):14651-8. doi: 10.1021/ja804427q. Epub 2008 Oct 11.
Binuclear ruthenium complexes that bind DNA by threading intercalation have recently been found to exhibit an exceptional kinetic selectivity for long polymeric adenine-thymine (AT) DNA. A series of oligonucleotide hairpin duplexes containing a central tract of 6-44 alternating AT base pairs have here been used to investigate the nature of the recognition mechanism. We find that, above a threshold AT tract length corresponding to one helix turn of B-DNA, a dramatic increase in threading intercalation rate occurs. In contrast, such length dependence is not observed for rates of unthreading. Intercalation by any mechanism that depends on the open end of the hairpin was found not to be important in the series of oligonucleotides used, as verified by including in the study a hairpin duplex cyclized by a copper-catalyzed "click" reaction. Our observations are interpreted in terms of a conformational pre-equilibrium, determined by the length of the AT tract. We finally find that mismatches or loops in the oligonucleotide facilitate the threading process, of interest for the development of mismatch-recognizing probes.
最近发现,通过穿线插入方式与DNA结合的双核钌配合物对长链聚合腺嘌呤 - 胸腺嘧啶(AT)DNA表现出异常的动力学选择性。这里使用了一系列含有6 - 44个交替AT碱基对中央区域的寡核苷酸发夹双链体来研究识别机制的本质。我们发现,在对应于B - DNA一个螺旋圈的阈值AT区域长度以上,穿线插入速率会急剧增加。相比之下,解线速率未观察到这种长度依赖性。通过在研究中纳入由铜催化的“点击”反应环化的发夹双链体验证,在所使用的一系列寡核苷酸中,任何依赖于发夹开口端的插入机制都不重要。我们的观察结果根据由AT区域长度决定的构象预平衡来解释。我们最终发现,寡核苷酸中的错配或环有助于穿线过程,这对于开发错配识别探针具有重要意义。