Ito Toshiyuki, Inoue Akira, Sato Kae, Hosokawa Kazuo, Maeda Mizuo
Bioengineering Laboratory, Institute of Physical and Chemical Research (RIKEN), Wako, Saitama 351-0198, Japan.
Anal Chem. 2005 Aug 1;77(15):4759-64. doi: 10.1021/ac050122f.
We have developed an extremely simple method for microchip electrophoresis. Loading of a sieving polymer solution and injection of a sample solution are autonomously executed by a microchip fabricated in poly(dimethylsiloxane) (PDMS). In advance, the energy for the fluid pumping is stored in bulk PDMS by evacuating air dissolved in PDMS, and the information for the sample plug regulation is coded into the microchannel design. Besides the simplicity, our method brings about an advantageous effect: sample compaction due to the discontinuous electrophoretic mobility at the sample/polymer interface. The sample compaction effect was moderate in ordinary size-dependent separation for double-stranded DNA and was extreme in affinity electrophoresis for single-stranded DNA (ssDNA). In the latter separation mode, ssDNA components were sequence-specifically separated by difference in affinity to a probe oligonucleotide immobilized to the sieving polymer matrix. We separated up to 60-mer ssDNA mixtures based on single-base substitutions. The separation processes included typically 100-fold sample compaction and were completed within 15-30 s. This technology provides easy, simple, and sensitive method for detection of gene point mutations and typing of single-nucleotide polymorphisms.
我们开发了一种用于微芯片电泳的极其简单的方法。筛分聚合物溶液的加载和样品溶液的注入由聚二甲基硅氧烷(PDMS)制成的微芯片自动执行。预先通过抽空溶解在PDMS中的空气将流体泵送所需的能量存储在块状PDMS中,并且将样品塞调节信息编码到微通道设计中。除了简单之外,我们的方法还带来了一个有利的效果:由于样品/聚合物界面处不连续的电泳迁移率导致样品压缩。在双链DNA的普通尺寸依赖性分离中,样品压缩效果适中,而在单链DNA(ssDNA)的亲和电泳中则极为显著。在后一种分离模式中,ssDNA组分通过与固定在筛分聚合物基质上的探针寡核苷酸的亲和力差异进行序列特异性分离。我们基于单碱基替换分离了长达60个碱基的ssDNA混合物。分离过程通常包括100倍的样品压缩,并在15 - 30秒内完成。该技术为基因点突变检测和单核苷酸多态性分型提供了简便、灵敏的方法。