Blazej Robert G, Kumaresan Palani, Cronier Samantha A, Mathies Richard A
UCSF/UC Berkeley Joint Bioengineering Graduate Group, University of California, Berkeley, California 94720, USA.
Anal Chem. 2007 Jun 15;79(12):4499-506. doi: 10.1021/ac070126f. Epub 2007 May 12.
A new affinity-capture-based inline purification, concentration, and injection method is developed for microchip capillary electrophoresis (CE) and used to perform efficient attomole-scale Sanger DNA sequencing separations. The microdevice comprises three axial domains for nanoliter-scale sequencing sample containment, sample plug formation, and high-resolution capillary gel electrophoresis. Purified and concentrated inline sample plugs are formed by electrophoretically driving Sanger sequencing extension fragments into an affinity-capture polymer network positioned within a CE separation channel. Extension fragments selectively hybridize and concentrate at the polymer interface while residual primer, nucleotides, and salts electrophorese out of the system. The plug is thermally released and injected into the CE channel by direct application of the separation voltage. To evaluate this system, 30 nL of sequencing sample prepared from 100 amol (60 million molecules) of human mitochondrial hypervariable region II amplicon was introduced into the microchip, purified, concentrated, and injected, generating a read length of 365 bases with 99% accuracy. This efficient inline injection system obviates the need for the excess sample that is required by cross-injection techniques, thereby enabling Sanger sequencing and other high-performance genetic analysis using DNA quantities approaching theoretical detection limits.
一种基于亲和捕获的新型在线纯化、浓缩和进样方法被开发用于微芯片毛细管电泳(CE),并用于进行高效的阿托摩尔级桑格DNA测序分离。该微型装置包括三个轴向区域,用于纳升规模的测序样品容纳、样品塞形成和高分辨率毛细管凝胶电泳。通过将桑格测序延伸片段电泳驱动到位于CE分离通道内的亲和捕获聚合物网络中,形成纯化和浓缩的在线样品塞。延伸片段在聚合物界面处选择性杂交并浓缩,而残留的引物、核苷酸和盐则电泳出系统。通过直接施加分离电压,将样品塞热释放并注入CE通道。为了评估该系统,将从100阿托摩尔(6000万个分子)的人线粒体高变区II扩增子制备的30纳升测序样品引入微芯片,进行纯化、浓缩和进样,产生了365个碱基的读长,准确率为99%。这种高效的在线进样系统消除了交叉进样技术所需的过量样品的需求,从而能够使用接近理论检测限的DNA量进行桑格测序和其他高性能基因分析。