Free-solution electrophoresis of DNA modified with drag-tags at both ends

被引:25
作者
Meagher, Robert J.
McCormick, Laurette C.
Haynes, Russell D.
Won, Jong-In
Lin, Jennifer S.
Slater, Gary W.
Barron, Annelise E.
机构
[1] Northwestern Univ, Dept Biol & Chem Engn, Evanston, IL 60208 USA
[2] Univ Ottawa, Dept Phys, Ottawa, ON, Canada
[3] Northwestern Univ, Dept Chem, Evanston, IL USA
关键词
dNA sequencing; drag-tags; end-labeled free-solution electrophoresis; genotyping; molecular end-effect;
D O I
10.1002/elps.200500554
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In end-labeled free-solution electrophoresis (ELFSE), DNA molecules are labeled with a frictional modifier or "drag-tag", allowing their size-based electrophoretic separation in free solution. Among the interesting observations from early work with dsDNA using streptavidin as a drag-tag was that the drag induced by including a streptavidin label at both ends was significantly more than double that from a single streptavidin (Heller, C. et al., J. Chromatogr A 1998, 806, 113-121). This finding was assumed to be in error, and subsequent work focused on experiments in which only a single drag-tag is appended to one end of the DNA molecule. Recent theoretical work (McCormick, L. C., Slater, G. W., Electrophoresis 2005, 26,1659-1667) has examined the contribution of end-effects to the free-solution electrophoretic mobility of charged-uncharged polymer conjugates, reopening the question of enhanced drag from placing a drag-tag at both ends. In this study, this effect is investigated experimentally, using custom-synthesized ssDNA oligonucleotides allowing the attachment of drag-tags to one or both ends, as well as dsDNA PCR products generated with primers appropriate for the attachment of drag-tags at one or both ends. A range of sizes of drag-tags are used, including synthetic polypeptoid drag-tags as well as genetically engineered protein polymer drag-tags. The enhanced drag arising from labeling both ends has been confirmed, with 6-9% additional drag for the ssDNA and 10-23% additional drag for the dsDNA arising from labeling both ends than would be expected from simply doubling the size of the drag-tag at one end. The experimental results for ssDNA labeled at both ends are compared to the predictions of the recent theory of end-effects, with reasonably good quantitative agreement. These experimental findings demonstrate the feasibility of enhancing ELFSE separations by labeling both ends of the DNA molecule, leading to greater resolving power and a wider range of applications for this technique.
引用
收藏
页码:1702 / 1712
页数:11
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