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基于微加工电泳装置的DNA测序

DNA sequencing on microfabricated electrophoretic devices.

作者信息

Schmalzing D, Adourian A, Koutny L, Ziaugra L, Matsudaira P, Ehrlich D

机构信息

Whitehead Institute for Biomedical Research, Nine Cambridge Center, Massachusetts 02142, USA.

出版信息

Anal Chem. 1998 Jun 1;70(11):2303-10. doi: 10.1021/ac971381a.

Abstract

We present a model that quantitatively describes the performance of microfabricated electrophoretic devices filled with linear polyacrylamide as replaceable sieving material for single-stranded DNA analyses. The dependence of resolution on various separation parameters such as selectivity, diffusion, injector size, device length, and channel folding was investigated. A previously predicted dependence of longitudinal diffusion coefficient on electric field strength has been verified. We have used this model to develop and optimize microfabricated electrophoretic devices for DNA analyses. For single-color DNA sequencing mixtures, we routinely achieve separations of 400 bases in under 14 min at 200 V/cm, and separation of 350 bases in only 7 min at 400 V/cm, with a minimum resolution of R = 0.5. Our results also indicate reduced fragment biasing and efficient sample stacking for DNA sample loading on microfabricated devices.

摘要

我们提出了一个模型,该模型定量描述了填充线性聚丙烯酰胺作为单链DNA分析的可替换筛分材料的微制造电泳装置的性能。研究了分辨率对各种分离参数的依赖性,如选择性、扩散、进样器尺寸、装置长度和通道折叠。先前预测的纵向扩散系数对电场强度的依赖性已得到验证。我们已使用此模型来开发和优化用于DNA分析的微制造电泳装置。对于单色DNA测序混合物,我们通常在200 V/cm下14分钟内实现400个碱基的分离,在400 V/cm下仅7分钟内实现350个碱基的分离,最小分辨率为R = 0.5。我们的结果还表明,在微制造装置上进行DNA样品加载时,片段偏倚减少,样品堆积高效。

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