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Soper, Steven A.
Soper Research Group
Research Interests
  • Micro- and nano-fabrication
  • Lab-on-a-chip
  • Polymeric Microfluidic Devices

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EndoV/DNA ligase mutation scanning assay using microchip capillary electrophoresis and dual-color laser-induced fluorescence detection

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Title
EndoV/DNA ligase mutation scanning assay using microchip capillary electrophoresis and dual-color laser-induced fluorescence detection
Author
Kotani, AkiraWitek, Malgorzata A.Osiri, John K.Wang, HongSinville, RondedrickPincas, HannaBarany, FrancisSoper, Steven A.
Keywords
Capillary gel electrophoresis; Cleavage products; DNA fragment; DNA ligases; DNA samples; Electropherograms; Endonucleases; Genomic DNA; High sensitivity; Highly sensitive; Hydroxyethyl cellulose; Laser induced fluorescence; Laser induced fluorescence detection; Low level; Microchip capillary electrophoresis; Microchip separations; PCR products; Polyacrylamide gels; Wild types
Issue Date
2012-01
Publisher
ROYAL SOC CHEMISTRY
Citation
ANALYTICAL METHODS, v.4, no.1, pp.58 - 64
Abstract
We report the ability to detect with high sensitivity sporadic mutations using a mutation scanning assay, which employs thermostable endonuclease V (EndoV) and DNA ligase. The products of the mutation scanning assay were separated using microchip capillary electrophoresis (mu CE) and detected with a dual-color laser-induced fluorescence (LIF) detector. PCR products from mutant and wild-type DNA of p53 exon 8 were generated using Cy3-labeled forward and Cy5-labeled reverse primers to allow LIF detection with mCE. EndoV recognizes and primarily cleaves heteroduplexed DNA one base 30 to a mismatch and can nick matched sites at low levels as well. DNA ligase is used to reseal nicks generated at matched sites, which creates a highly sensitive and specific assay for analyzing sporadic mutations in genomic DNA. Heteroduplexed DNA samples were treated with EndoV alone and with both EndoV and DNA ligase and separated using a 4% (w/v) linear polyacrylamide gel constituted in 1x TTE buffer, 7 M urea, and 0.05% (w/v) methyl hydroxyethyl cellulose, which was used to suppress the EOF in the microchip. Sizing of the bands appearing in the electropherogram revealed the approximate position of the mutation. In this study, mutations present in p53 exon 8 generated Cy3-labeled cleavage products of 158 nt and Cy5-labeled cleavage products of 195 nt. The DNA fragments were simultaneously monitored at their respective color using a dual-color LIF system with the 158 and 195 nt fragments detected along with heteroduplexed fragments of 350 nt. The microchip separation was completed within 7 min, almost tenfold shorter time compared to conventional capillary gel electrophoresis.
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DOI
10.1039/c1ay05366c
ISSN
1759-9660
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PHY_Journal Papers
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