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Membrane‐mediated ultrafast restriction digestion and subsequent rapid gel microchip electrophoresis of DNA
Author(s) -
Guttman András,
Ronai Zsolt,
Barta Csaba,
Hou YuMing,
SasvariSzekely Maria,
Wang Xun,
Briggs Steven P.
Publication year - 2002
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200205)23:10<1524::aid-elps1524>3.0.co;2-y
Subject(s) - restriction enzyme , restriction digest , gel electrophoresis , digestion (alchemy) , chromatography , electrophoresis , chemistry , gel electrophoresis of nucleic acids , dna , microscale chemistry , molecular weight size marker , polyacrylamide gel electrophoresis , gel electrophoresis of proteins , biochemistry , enzyme , mathematics education , mathematics
Ultrafast, membrane‐mediated restriction digestion of DNA molecules followed by rapid gel microchip electrophoresis of the resulting fragments is described. Combination of restriction endonuclease digestion on small pore‐size microfibrous membranes with sample loading and electrophoresis analysis in a multilane (up to 96) format resulted in very fast restriction digest based microscale DNA analysis. Complete digestion of several nanogram target DNA was accomplished on the microporous membrane at room temperature just in a few minutes with a single or a combination of various restriction enzymes, using only submicroliter quantities of samples and reagents. The reaction mixture containing membrane also served as sample loading device for the subsequent gel microchip electrophoresis based analysis. This work establishes methods for high‐speed, high‐hroughput DNA analysis, featuring extremely low sample and reagent consumption, and fast restriction digestion in combination with sample loading and rapid gel microchip analysis of the resulting fragments. The entire restriction digestion, sample loading and electrophoresis analysis process required less than 20 min.