Trapping of megabase-sized DNA molecules during agarose gel electrophoresis
Author(s) -
Sergio Gurrieri,
Steven B. Smith,
Carlos Bustamante
Publication year - 1999
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.96.2.453
Subject(s) - trapping , electrophoresis , gel electrophoresis , agarose , gel electrophoresis of nucleic acids , molecule , agarose gel electrophoresis , pulsed field gel electrophoresis , dna , chemistry , materials science , biology , chromatography , biochemistry , ecology , organic chemistry , gene , genotype
Megabase DNA molecules become trapped in agarose gels during electrophoresis if the electric field exceeds a few volts per cm. Fluorescence microscopy reveals that these molecules invariably arrest in U-shaped conformations. The field-vs.-size dependence for trapping indicates that a critical molecular tension is required for trapping. The size of unligated lambda-ladders, sheared during gel electrophoresis at a given field, coincides with the size of molecules trapped at that field, suggesting that both processes occur through nick melting near the vertex of the U-shape. Consistently, molecules nicked by exposure to UV radiation trap more readily than unexposed ones. The critical trapping tension at the vertex is estimated to be 15 pN, a force sufficient to melt nicks bent around gel fibers, and, according to our model, trap a molecule. Strategies to reduce molecular tension and avoid trapping are discussed.
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