Molecular deformation and free-solution electrophoresis of DNA-uncharged polymer conjugates at high field strengths: Theoretical predictions - Part 2: Stretching

被引:7
作者
McCormick, Laurette C. [1 ]
Slater, Gary W. [1 ]
机构
[1] Univ Ottawa, Dept Phys, Ottawa, ON K1N 6N5, Canada
关键词
DNA sequencing; electrophoretic mobility; end-labeled free-solution electrophoresis; free-solution electrophoresis; polymer deformation;
D O I
10.1002/elps.200600838
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DNA sequencing by electrophoresis can be dramatically sped up by overcoming the need for the sieving medium. Normally it is possible to separate DNA based on size in free solution; however, not end-labeled free-solution electrophoresis (ELFSE) uses a neutral drag-tag molecule to make it possible. In experiments to date, the drag-tag and DNA together form a random coil conformation; while with future generation drag-tags and high fields, deformation of this conformation may occur. In the first paper in this series we investigated the conditions under which the DNA and label become hydrodynamically distinct (or segregated), based on a theoretical approach developed for the electrophoresis of polyampholytes. In this paper we study further deformation wherein either the DNA and/or a polymeric label stretch. We show that deformation may dramatically improve the capabilities of ELFSE, especially when both the DNA and a polymeric drag-tag fully stretch; however, reaching these regimes will require extremely high field intensifies, something that only microchip technologies may be able to achieve.
引用
收藏
页码:3837 / 3844
页数:8
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