Simpson J W, Ruiz-Martinez M C, Mulhern G T, Berka J, Latimer D R, Ball J A, Rothberg J M, Went G T
CuraGen Corporation, New Haven, CT 06511, USA.
Electrophoresis. 2000 Jan;21(1):135-49. doi: 10.1002/(SICI)1522-2683(20000101)21:1<135::AID-ELPS135>3.0.CO;2-U.
In this paper we present the development of a DNA analysis system using a microfabricated channel device and a novel transmission imaging spectrograph which can be efficiently incorporated into a high throughput genomics facility for both sizing and sequencing of DNA fragments. The device contains 48 channels etched on a glass substrate. The channels are sealed with a flat glass plate which also provides a series of apertures for sample loading and contact with buffer reservoirs. Samples can be easily loaded in volumes up to 640 nL without band broadening because of an efficient electrokinetic stacking at the electrophoresis channel entrance. The system uses a dual laser excitation source and a highly sensitive charge-coupled device (CCD) detector allowing for simultaneous detection of many fluorescent dyes. The sieving matrices for the separation of single-stranded DNA fragments are polymerized in situ in denaturing buffer systems. Examples of separation of single-stranded DNA fragments up to 500 bases in length are shown, including accurate sizing of GeneCalling fragments, and sequencing samples prepared with a reduced amount of dye terminators. An increase in sample throughput has been achieved by color multiplexing.
在本文中,我们展示了一种DNA分析系统的开发,该系统使用了一种微制造通道装置和一种新型透射成像光谱仪,它可以高效地整合到高通量基因组学设备中,用于DNA片段的大小测定和测序。该装置在玻璃基板上蚀刻有48个通道。这些通道用一块平板玻璃板密封,平板玻璃板还提供了一系列用于样品加载以及与缓冲液储液器接触的孔。由于在电泳通道入口处有高效的电动堆积,样品可以轻松加载,体积可达640 nL且不会出现条带展宽。该系统使用双激光激发源和高灵敏度电荷耦合器件(CCD)探测器,能够同时检测多种荧光染料。用于分离单链DNA片段的筛分基质在变性缓冲液系统中原位聚合。展示了长度达500个碱基的单链DNA片段的分离示例,包括对基因分型片段的精确大小测定,以及用减少量的染料终止剂制备的测序样品。通过颜色复用实现了样品通量的增加。