Gurrieri S, Smith S B, Bustamante C
Dipartimento di Scienze Chimiche, Universitá di Catania, Viale A. Doria 6, 95125 Catania, Italy.
Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):453-8. doi: 10.1073/pnas.96.2.453.
Megabase DNA molecules become trapped in agarose gels during electrophoresis if the electric field exceeds a few volts per cm. Fluorescence microscopy reveals that these molecules invariably arrest in U-shaped conformations. The field-vs.-size dependence for trapping indicates that a critical molecular tension is required for trapping. The size of unligated lambda-ladders, sheared during gel electrophoresis at a given field, coincides with the size of molecules trapped at that field, suggesting that both processes occur through nick melting near the vertex of the U-shape. Consistently, molecules nicked by exposure to UV radiation trap more readily than unexposed ones. The critical trapping tension at the vertex is estimated to be 15 pN, a force sufficient to melt nicks bent around gel fibers, and, according to our model, trap a molecule. Strategies to reduce molecular tension and avoid trapping are discussed.
如果电场强度超过每厘米几伏,兆碱基DNA分子在电泳过程中就会被困在琼脂糖凝胶中。荧光显微镜显示,这些分子总是以U形构象停滞。捕获的电场与大小的依赖性表明,捕获需要临界分子张力。在给定电场下进行凝胶电泳时剪切的未连接λ阶梯的大小,与在该电场下捕获的分子大小一致,这表明这两个过程都是通过U形顶点附近的切口熔解发生的。一致的是,暴露于紫外线辐射而产生切口的分子比未暴露的分子更容易捕获。顶点处的临界捕获张力估计为15皮牛,这一力足以熔解围绕凝胶纤维弯曲的切口,并且根据我们的模型,可以捕获一个分子。文中还讨论了降低分子张力并避免捕获的策略。