Zheng Jinjian, Yeung Edward S
Ames Laboratory--USDOE, Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.
Anal Chem. 2003 Aug 1;75(15):3675-80. doi: 10.1021/ac034430u.
We demonstrate a novel separation mechanism for large molecules based on their radial migration in capillary electrophoresis with applied hydrodynamic flow (HDF). The direction of radial migration depends on the direction of the applied HDF relative to the electric field. The radial migration velocities are size-dependent, which could be attributed to the different degree of deformation under shear flow. Analytical separation was demonstrated on a sample plug containing lambda DNA (48 502 bp) and phiX174 RF DNA (5386 bp) with baseline separation. Alternatively, this separation mode can be performed continuously and is thus applicable to preparative separations. Without the need for gel/polymer or complex instrumentation, this separation technique is complementary to capillary gel electrophoresis and field-flow fractionation. Although large DNA molecules were used to demonstrate the separation mechanism here, these protocols could also be applied to the separation of proteins, cells, or particles based on size, shape, or deformability.
我们展示了一种基于大分子在施加流体动力流(HDF)的毛细管电泳中的径向迁移的新型分离机制。径向迁移的方向取决于施加的HDF相对于电场的方向。径向迁移速度与大小有关,这可归因于剪切流下不同程度的变形。在含有λDNA(48502 bp)和φX174 RF DNA(5386 bp)的样品塞中进行了分析分离,并实现了基线分离。此外,这种分离模式可以连续进行,因此适用于制备分离。无需凝胶/聚合物或复杂仪器,这种分离技术是毛细管凝胶电泳和场流分级分离的补充。尽管这里使用大DNA分子来证明分离机制,但这些方案也可应用于基于大小、形状或可变形性的蛋白质、细胞或颗粒的分离。