首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Influence of branch length asymmetry on the electrophoretic mobility of rigid rod-like DNA
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Influence of branch length asymmetry on the electrophoretic mobility of rigid rod-like DNA

机译:分支长度不对称性对刚性杆状DNA电泳迁移率的影响

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摘要

The electrophoretic mobility of three-arm asymmetric star DNA molecules, produced by incorporating a short DNA branch at the midpoint of rigid-rod linear DNA fragments, is investigated in polyacrylamide gels. We determine how long the added branch must be to separate asymmetric star DNA from linear DNA with the same total molecular weight. This work focuses on two different geometric progressions of small DNA molecules. First, branches of increasing length were introduced at the center of a linear DNA fragment of constant length. At a given gel concentration, we find that relatively small branch lengths are enough to cause a detectable reduction in electrophoretic mobility. The second geometric progression starts with a small branch on a linear DNA fragment. As the length of this branch is increased, the DNA backbone length is decreased such that the total molar mass of the molecule remains constant. The branch length was then increased until the asymmetric branched molecule becomes a symmetric three-arm star polymer, allowing the effect of molecular topology on mobility to be studied independent of size effects. DNA molecules with very short branches have a mobility smaller than linear DNA of identical molar mass. The reason for this change in mobility when branching is introduced is not known, however, we explore two possible explanations in this article. (i) The branched DNA could have a greater interaction with the gel than linear DNA, causing it to move slower; (ii) the linear DNA could have modes of motion or access to pores that are unavailable to the branched DNA.
机译:在聚丙烯酰胺凝胶中研究了三臂不对称星形DNA分子的电泳迁移率,该分子是通过在刚性杆线性DNA片段的中点掺入短的DNA分支而产生的。我们确定将总分子量相同的不对称星形DNA与线性DNA分开必须增加的时间。这项工作着眼于小DNA分子的两种不同的几何级数。首先,在恒定长度的线性DNA片段的中心引入长度增加的分支。在给定的凝胶浓度下,我们发现相对较小的分支长度足以引起电泳迁移率的可检测降低。第二个几何级数以线性DNA片段上的小分支开始。随着该分支的长度增加,DNA主链长度减少,从而使分子的总摩尔质量保持恒定。然后增加支链的长度,直到不对称的支链分子变成对称的三臂星形聚合物,从而可以独立于尺寸效应研究分子拓扑对迁移率的影响。具有非常短的分支的DNA分子的迁移率小于相同摩尔质量的线性DNA。引入分支时迁移率发生这种变化的原因尚不清楚,但是,我们在本文中探讨了两种可能的解释。 (i)支链DNA与凝胶的相互作用可能比线性DNA大,从而使其移动较慢; (ii)线性DNA可能具有运动模式或进入分支DNA无法获得的孔。

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