Lin Yen-Heng, Chang Chen-Min, Lee Gwo-Bin
Department of Engineering Science, National Cheng Kung University, Tainan, Taiwan.
Opt Express. 2009 Aug 17;17(17):15318-29. doi: 10.1364/oe.17.015318.
A new platform is presented that is capable of manipulating a single DNA molecule based on optically-induced dielectrophoretic forces. The ends of a single DNA molecule are bound with a micro-bead, which is then manipulated by interactions with optical images projected from a commercially available projector. Thus a single DNA molecule is indirectly manipulated by a projected animation pre-programmed using simple computer software. Real-time observation of the manipulation process is made possible by using a fluorescent dye and an oxygen scavenging buffer. Two types of DNA manipulation modes, specifically DNA elongation and rotation, are successfully demonstrated and are characterized. The maximum stretching force can be as high as 61.3 pN for a 10.1 microm bead. Experimental data show that the force-extension curve measured using this platform fits reasonably with the worm-like chain model. The developed platform can be a promising and flexible tool for further applications requiring single molecule manipulation.
本文提出了一种新平台,该平台能够基于光诱导介电泳力来操纵单个DNA分子。单个DNA分子的末端与一个微珠相连,然后通过与从市售投影仪投射的光学图像相互作用来操纵该微珠。因此,单个DNA分子通过使用简单计算机软件预编程的投影动画进行间接操纵。通过使用荧光染料和氧气清除缓冲液,可以对操纵过程进行实时观察。成功演示并表征了两种类型的DNA操纵模式,即DNA伸长和旋转。对于一个10.1微米的珠子,最大拉伸力可高达61.3皮牛。实验数据表明,使用该平台测量的力-伸长曲线与蠕虫状链模型合理拟合。所开发的平台对于需要单分子操纵的进一步应用可能是一种有前途且灵活的工具。