Bucka Alexander, Stasiak Andrzej
Laboratoire d'Analyse Ultrastructurale, Université de Lausanne, 1015 Lausanne-Dorigny, Switzerland.
Nucleic Acids Res. 2002 Mar 15;30(6):e24. doi: 10.1093/nar/30.6.e24.
In recent years there has been growing interest in the question of how the particular topology of polymeric chains affects their overall dimensions and physical behavior. The majority of relevant studies are based on numerical simulation methods or analytical treatment; however, both these approaches depend on various assumptions and simplifications. Experimental verification is clearly needed but was hampered by practical difficulties in obtaining preparative amounts of knotted or catenated polymers with predefined topology and precisely set chain length. We introduce here an efficient method of production of various single-stranded DNA knots and catenanes that have the same global chain length. We also characterize electrophoretic migration of the produced single-stranded DNA knots and catenanes with increasing complexity.
近年来,人们越来越关注聚合物链的特定拓扑结构如何影响其整体尺寸和物理行为这一问题。大多数相关研究基于数值模拟方法或解析处理;然而,这两种方法都依赖于各种假设和简化。显然需要实验验证,但由于难以制备出具有预定义拓扑结构和精确设定链长的打结或连环聚合物,实际操作存在困难,这一验证受到了阻碍。我们在此介绍一种生产具有相同全局链长的各种单链DNA结和连环体的有效方法。我们还对所制备的单链DNA结和连环体随着复杂度增加的电泳迁移特性进行了表征。