Department of Biophysical Engineering, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, 7500 AE Enschede, The Netherlands.
Nucleic Acids Res. 2010 Jun;38(10):3423-31. doi: 10.1093/nar/gkq034. Epub 2010 Feb 2.
When individual dsDNA molecules are stretched beyond their B-form contour length, they reveal a structural transition in which the molecule extends 1.7 times its contour length. The nature of this transition is still a subject of debate. In the first model, the DNA helix unwinds and combined with the tilting of the base pairs (which remain intact), results in a stretched form of DNA (also known as S-DNA). In the second model the base pairs break resulting effectively in two single-strands, which is referred to as force-induced melting. Here a combination of optical tweezers force spectroscopy with fluorescence microscopy was used to study the structure of dsDNA in the overstretching regime. When dsDNA was stretched in the presence of 10 nM YOYO-1 an initial increase in total fluorescence intensity of the dye-DNA complex was observed and at an extension where the dsDNA started to overstretch the fluorescence intensity leveled off and ultimately decreased when stretched further into the overstretching region. Simultaneous force spectroscopy and fluorescence polarization microscopy revealed that the orientation of dye molecules did not change significantly in the overstretching region (78.0 degrees +/- 3.2 degrees). These results presented here clearly suggest that, the structure of overstretched dsDNA can be explained accurately by force induced melting.
当单个 dsDNA 分子被拉伸超出其 B 型轮廓长度时,它们会发生结构转变,分子伸展至其轮廓长度的 1.7 倍。这种转变的性质仍然存在争议。在第一个模型中,DNA 螺旋解开,并与碱基对的倾斜(保持完整)相结合,导致 DNA 的伸展形式(也称为 S-DNA)。在第二个模型中,碱基对断裂,实际上导致两条单链,这被称为力诱导熔化。在这里,我们结合使用光学镊子力谱学和荧光显微镜来研究过度拉伸状态下 dsDNA 的结构。当 dsDNA 在 10 nM YOYO-1 的存在下被拉伸时,观察到染料-DNA 复合物的总荧光强度最初增加,并且当 dsDNA 开始过度拉伸时,荧光强度趋于平稳,并且当进一步拉伸到过度拉伸区域时最终降低。同时进行力谱学和荧光偏振显微镜揭示,在过度拉伸区域(78.0 度 +/- 3.2 度)中染料分子的取向没有显著变化。这里呈现的结果清楚地表明,过度拉伸的 dsDNA 的结构可以通过力诱导熔化准确地解释。