Sattin Bernie D, Pelling Andrew E, Goh M Cynthia
Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada.
Nucleic Acids Res. 2004 Sep 14;32(16):4876-83. doi: 10.1093/nar/gkh826. Print 2004.
The forces that hold complementary strands of DNA together in a double helix, and the role of base mismatches in these, are examined by single molecule force spectroscopy using an atomic force microscope (AFM). These forces are important when considering the binding of proteins to DNA, since these proteins often mechanically stretch the DNA during their action. In AFM measurement of forces, there is an inherent instrumental limitation that makes it difficult to compare results from different experimental runs. This is circumvented by using an oligonucleotide microarray, which allowed a direct comparison of the forces between perfectly matched short oligonucleotides and those containing a single or double mismatch. Through this greatly increased sensitivity, the force contribution of a single AT base pair was derived. The results indicate that the contribution to forces from the stacking interactions is more important than that from hydrogen bonding.
利用原子力显微镜(AFM)通过单分子力谱研究了在双螺旋结构中将DNA互补链维系在一起的作用力以及碱基错配在其中的作用。在考虑蛋白质与DNA的结合时,这些作用力很重要,因为这些蛋白质在其作用过程中常常会机械性地拉伸DNA。在AFM力测量中,存在一个固有的仪器限制,使得不同实验运行的结果难以比较。通过使用寡核苷酸微阵列可避免这一问题,寡核苷酸微阵列能够直接比较完全匹配的短寡核苷酸与含有一个或两个错配的寡核苷酸之间的作用力。通过这种大幅提高的灵敏度,得出了单个AT碱基对的力贡献。结果表明,堆积相互作用对作用力的贡献比氢键的贡献更为重要。