Kumagai Hidesato, Utsunomiya Shinichi, Nakamura Shin, Yamamoto Rintaro, Harada Akira, Kaji Toru, Hazama Makoto, Ohashi Tetsuo, Inami Atsushi, Ikegami Takashi, Miyamoto Keisuke, Endo Naoya, Yoshimi Kenichi, Toyoda Atsushi, Hattori Masahira, Sakaki Yoshiyuki
Shimadzu Corporation, Kyoto, Japan.
Electrophoresis. 2008 Dec;29(23):4723-32. doi: 10.1002/elps.200800301.
We have described a new DNA sequencing platform based on the Sanger chemistry, in which the large-scale microfabricated channel plates and electrophoretic system result in higher-throughput DNA sequencing. Three hundred and eighty-four channels are arranged in a fan-like shape on a 25x47 cm glass plate, on which 384 oval sample holes are connected to each channel coupled to the opposite anode access holes. Two microfabricated plates are set on the sequencing apparatus, in which sequencing electrophoresis is conducted on one plate and the preparation process is on another plate. Each sample hole is loaded with 2.3 microL volume of sample and injected into separation channels electrokinetically. High-quality sequencing data were acquired using the pUC18 template, achieving an average read-length of 1001 bases with 99% accuracy and a throughput of 5 Mbases per day per instrument. To assess the performance in actual sequencing field, the bacterial artificial chromosome shotgun library of the Pseudorca crassidens genome was sequenced, using 1/80 of the quantity of Sanger reagent (0.1 microL). We believe that this is the first demonstration of the useful performance of DNA sequencing using monolithic microfabricated devices with walk-away operation.
我们描述了一种基于桑格化学法的新型DNA测序平台,其中大规模微制造通道板和电泳系统实现了更高通量的DNA测序。384个通道呈扇形排列在一块25×47厘米的玻璃板上,板上有384个椭圆形样品孔,每个样品孔与连接到相对阳极接入孔的通道相连。测序仪器上设置了两块微制造板,一块用于进行测序电泳,另一块用于制备过程。每个样品孔装载2.3微升体积的样品,并通过电动方式注入分离通道。使用pUC18模板获得了高质量的测序数据,平均读长为1001个碱基,准确率为99%,每台仪器每天的通量为5兆碱基。为了评估在实际测序领域的性能,对糙齿海豚基因组的细菌人工染色体鸟枪法文库进行了测序,使用的桑格试剂数量为正常用量的1/80(0.1微升)。我们认为,这是首次展示使用具有无需值守操作的整体微制造设备进行DNA测序的实用性能。