Kozulić B
Guest Elchrom Scientific AG, Cham, Switzerland.
Appl Theor Electrophor. 1994;4(3):149-59.
The door-corridor model of gel electrophoresis enabled an estimation of the net charge of DNA molecules run in various gels. When the runs were carried out in Trisacetate-EDTA buffer having a concentration from 10 to 120 mM, the net charge in 1% agarose gel varied from 1.1 to 0.58 e per base pair. The friction between migrating molecules and gel fibers was dependent on the gel type and concentration, as well as the electric field strength and temperature during electrophoresis. In the 123 to 1,474 bp size range, the friction in 1% agarose changed from 1.91 to 378.03 x 10(-10) N.m-1.s. It was found that the friction per 123 bp DNA segment is not constant, but raises with size. The gel resistance force increases at higher electric field strengths, indicating that elastic forces govern the migration of macromolecules through gels. In the gels studied, the friction, and therefore thermal diffusion, of DNA and protein-SDS complexes scale with from 2.20 to 2.32 power of size. The ratio of thermally induced diffusion and velocity in various gels shows that there is a profound reduction of diffusion compared to velocity with increasing DNA size. This is directly linked to the high exponent relating friction and size. The high resolving power of gel electrophoresis can be correlated to the difference between the frictional coefficients of a diffusing and migrating macromolecule.
凝胶电泳的门廊模型能够估算在各种凝胶中运行的DNA分子的净电荷。当在浓度为10至120 mM的Tris乙酸盐-EDTA缓冲液中进行电泳时,1%琼脂糖凝胶中的净电荷每碱基对从1.1 e变化到0.58 e。迁移分子与凝胶纤维之间的摩擦力取决于凝胶类型和浓度,以及电泳过程中的电场强度和温度。在123至1474 bp的大小范围内,1%琼脂糖中的摩擦力从1.91×10⁻¹⁰ N·m⁻¹·s变化到378.03×10⁻¹⁰ N·m⁻¹·s。发现每123 bp DNA片段的摩擦力不是恒定的,而是随大小增加。在较高电场强度下凝胶阻力增加,表明弹性力控制着大分子在凝胶中的迁移。在所研究的凝胶中,DNA和蛋白质-SDS复合物的摩擦力以及因此的热扩散与大小的2.20至2.32次方成比例。在各种凝胶中热诱导扩散与速度的比率表明,随着DNA大小增加,扩散与速度相比有显著降低。这直接与摩擦力和大小之间的高指数相关。凝胶电泳的高分辨率可以与扩散和迁移大分子的摩擦系数差异相关联。