Perkins T T, Quake S R, Smith D E, Chu S
Department of Physics, Stanford University, CA 94305.
Science. 1994 May 6;264(5160):822-6. doi: 10.1126/science.8171336.
Single molecules of DNA, visualized in video fluorescence microscopy, were stretched to full extension in a flow, and their relaxation was measured when the flow stopped. The molecules, attached by one end to a 1-micrometer bead, were manipulated in an aqueous solution with optical tweezers. Inverse Laplace transformations of the relaxation data yielded spectra of decaying exponentials with distinct peaks, and the longest time component (tau) increased with length (L) as tau approximately L 1.68 +/- 0.10. A rescaling analysis showed that most of the relaxation curves had a universal shape and their characteristic times (lambda t) increased as lambda t approximately L 1.65 +/- 0.13. These results are in qualitative agreement with the theoretical prediction of dynamical scaling.
在视频荧光显微镜下可视化的单分子DNA在流动中被拉伸至完全伸展,当流动停止时测量其松弛情况。这些分子一端连接到一个1微米的珠子上,在水溶液中用光学镊子进行操作。松弛数据的拉普拉斯逆变换产生了具有明显峰值的衰减指数光谱,最长时间分量(τ)随长度(L)增加,τ约为L的1.68±0.10次方。重标度分析表明,大多数松弛曲线具有通用形状,其特征时间(λt)随λt约为L的1.65±0.13次方增加。这些结果与动态标度的理论预测在定性上一致。