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电泳拉伸DNA的方法:微收缩、凝胶以及凝胶-微收缩混合装置。

Methods to electrophoretically stretch DNA: microcontractions, gels, and hybrid gel-microcontraction devices.

作者信息

Randall Greg C, Schultz Kelly M, Doyle Patrick S

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, MIT Room 66-456, 77 Massachusetts Ave., Cambridge, MA 02139, USA.

出版信息

Lab Chip. 2006 Apr;6(4):516-25. doi: 10.1039/b515326c. Epub 2006 Mar 7.

Abstract

The ability to controllably and continuously stretch large DNA molecules in a microfluidic format is important for gene mapping technologies such as Direct Linear Analysis (DLA). We have recently shown that electric field gradients can be readily generated in a microfluidic device and the resulting field is purely elongational. We present a single molecule fluorescence microscopy analysis of T4 DNA (169 kbp) stretching in the electric field gradients in a hyperbolic contraction microchannel. In addition, we are able to selectively pattern a crosslinked gel anywhere inside the microchannel. With an applied electric field, DNA molecules are forced to reptate through the gel and they moderately stretch as they exit the gel. By placing a gel immediately in front of the hyperbolic contraction, we bypass "molecular individualism" and achieve highly uniform and complete stretching of T4 DNA.

摘要

以微流控形式可控且连续地拉伸大型DNA分子的能力对于诸如直接线性分析(DLA)等基因图谱技术至关重要。我们最近表明,在微流控装置中可以很容易地产生电场梯度,并且产生的场是纯拉伸场。我们展示了在双曲线收缩微通道中,T4 DNA(169 kbp)在电场梯度中拉伸的单分子荧光显微镜分析。此外,我们能够在微通道内的任何位置选择性地构建交联凝胶。施加电场后,DNA分子被迫通过凝胶进行蛇行运动,并且在离开凝胶时会适度拉伸。通过在双曲线收缩区域的正前方立即放置凝胶,我们绕过了“分子个体性”,实现了T4 DNA的高度均匀且完全的拉伸。

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