A DNA prism for high-speed continuous fractionation of large DNA molecules

被引:177
|
作者
Huang, LR
Tegenfeldt, JO
Kraeft, JJ
Sturm, JC
Austin, RH
Cox, EC [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Phys, Princeton, NJ 08544 USA
[3] Princeton Univ, Dept Elect Engn, Princeton, NJ 08544 USA
[4] Princeton Univ, Ctr Photon & Optoelect Mat POEM, Princeton, NJ 08544 USA
关键词
D O I
10.1038/nbt733
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The analysis and fractionation of large DNA molecules plays a key role in many genome projects. The standard method, pulsed-field gel electrophoresis (PFGE), is slow, with running times ranging from 10 hours to more than 200 hours. In this report, we describe a thumbnail-sized device that sorts large DNA fragments (61-209 kilobases (kb)) in 15 seconds, with a resolution of similar to13%. An array of micron-scale posts serves as the sieving matrix, and integrated microfluidic channels spatially shape the electric fields over the matrix. Asymmetric pulsed fields are applied for continuous-flow operation, which sorts DNA molecules in different directions according to their molecular masses, much as a prism deflects light of different wavelengths at different angles. We demonstrate the robustness of the device by using it to separate large DNA inserts prepared from bacterial artificial chromosomes, a widely used DNA source for most genomics projects.
引用
收藏
页码:1048 / 1051
页数:5
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