Noom Maarten C, van den Broek Bram, van Mameren Joost, Wuite Gijs J L
Physics of Complex Systems, Department of Physics and Astronomy, Faculty of Sciences, Vrije Universiteit, De Boelelaan 1081, 1081 HV Amsterdam, The Netherlands.
Nat Methods. 2007 Dec;4(12):1031-6. doi: 10.1038/nmeth1126. Epub 2007 Nov 11.
Many biological processes involve enzymes moving along DNA. Such motion might be impeded by DNA-bound proteins or DNA supercoils. Current techniques are incapable of directly measuring forces that such 'roadblocks' might impose. We constructed a setup with four independently moveable optical traps, allowing us to manipulate two DNA molecules held between beads. By tightly wrapping one DNA around the other, we created a probe that can be scanned along the contour of the second DNA. We found that friction between the two polymers remains below 1 pN. Upon encountering DNA-bound proteins substantial friction forces are measured, allowing accurate localization of protein positions. Furthermore, these proteins remained associated at low probe tensions but could be driven off using forces greater than 20 pN. Finally, the full control of the orientation of two DNA molecules opens a wide range of experiments on proteins interacting with multiple DNA regions.
许多生物过程都涉及酶沿着DNA移动。这种运动可能会受到与DNA结合的蛋白质或DNA超螺旋的阻碍。目前的技术无法直接测量这些“路障”可能施加的力。我们构建了一个带有四个独立可移动光学阱的装置,使我们能够操纵夹在珠子之间的两个DNA分子。通过将一个DNA紧紧缠绕在另一个DNA上,我们创建了一个可以沿着第二个DNA的轮廓进行扫描的探针。我们发现这两种聚合物之间的摩擦力保持在1皮牛以下。当遇到与DNA结合的蛋白质时,可以测量到很大的摩擦力,从而能够准确确定蛋白质的位置。此外,这些蛋白质在低探针张力下仍保持结合状态,但可以用大于20皮牛的力将其驱离。最后,对两个DNA分子取向的完全控制开启了一系列关于蛋白质与多个DNA区域相互作用的实验。