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在硅芯片热循环仪中对不同模板类型进行小型化流通式聚合酶链反应。

Miniaturized flow-through PCR with different template types in a silicon chip thermocycler.

作者信息

Schneegass I, Brautigam R, Kohler J M

机构信息

Institute for Physical High Technology (IPHT), Department of Biotechnical Micro Systems, Winzerlaer Str. 10, D-07745, Jena, Germany.

出版信息

Lab Chip. 2001 Sep;1(1):42-9. doi: 10.1039/b103846j. Epub 2001 Aug 9.

Abstract

Flow-through chip thermocyclers can be used in miniaturized rapid polymerase chain reaction (PCR) despite their high surface to volume ratio of samples. We demonstrated that a thermocycler made of silicon and glass chips and containing thin film transducers for heating and temperature control can be adapted to the amplification of various DNA templates of different sources and properties. Therefore, the concept of serial flow in a liquid/liquid two-phase system was combined with a surface management of inner side walls of the microchannel and an adaptation of PCR mixture composition. In addition, the process temperatures and the flow rates were optimized. Thus, a synthetic template originating from investigations on nucleic acid evolution with 106 base pairs [cooperative amplification of templates by cross hybridization (CATCH)], a house keeping gene with 379 base pairs [glutaraldehyde 3-phosphate dehydrogenase (GAPDH)] and a zinc finger protein relevant in human pathogenesis with 700 base pairs [Myc-interacting zinc finger protein-1, knock-out (Miz1-KO)] were amplified successfully. In all three cases the selectivity of priming and amplification could be shown by gel electrophoresis. The typical amplification time was 1 min per temperature cycle. So, the typical residence time of a sample volume inside the 25 cycle device amounts to less then half an hour. The energy consumption of the PCR chip for a 35 min PCR process amounts to less than 0.012 kW h.

摘要

尽管样品的表面积与体积之比很高,但流通式芯片热循环仪仍可用于小型化快速聚合酶链反应(PCR)。我们证明,由硅和玻璃芯片制成、包含用于加热和温度控制的薄膜换能器的热循环仪,可适用于扩增不同来源和性质的各种DNA模板。因此,将液/液两相系统中的连续流动概念与微通道内侧壁的表面处理以及PCR混合物组成的调整相结合。此外,还对工艺温度和流速进行了优化。因此,成功扩增了源自核酸进化研究的106个碱基对的合成模板[通过交叉杂交进行模板的协同扩增(CATCH)]、379个碱基对的管家基因[3-磷酸甘油醛脱氢酶(GAPDH)]以及与人类发病机制相关的700个碱基对的锌指蛋白[Myc相互作用锌指蛋白-1,敲除(Miz1-KO)]。在所有三种情况下,均可通过凝胶电泳显示引物和扩增的选择性。每个温度循环的典型扩增时间为1分钟。因此,在25个循环的装置中,样品体积的典型停留时间不到半小时。用于35分钟PCR过程的PCR芯片的能耗不到0.012千瓦·时。

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