Handmade microfluidic device for biochemical applications in emulsion

被引:3
|
作者
Murzabaev, Marsel [1 ]
Kojima, Takaaki [1 ]
Mizoguchi, Takuro [1 ]
Kobayashi, Isao [2 ]
DeKosky, Brandon J. [3 ]
Georgiou, George [3 ]
Nakano, Hideo [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648601, Japan
[2] NARO, Natl Food Res Inst, Food Engn Div, Tsukuba, Ibaraki 3058642, Japan
[3] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
关键词
Microfluidics; Flow-focusing; In vitro transcription/translation; In vitro compartmentalization; Monodisperse emulsion; IN-VITRO COMPARTMENTALIZATION; FREE PROTEIN-SYNTHESIS; LIGASE RIBOZYME; SELECTION; DISPLAY; DROPLETS; PCR; MICRODROPLETS; POLYMERASE;
D O I
10.1016/j.jbiosc.2015.08.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A simple, inexpensive flow-focusing device has been developed to make uniform droplets for biochemical reactions, such as in vitro transcription and cell-free protein synthesis. The device was fabricated from commercially available components without special equipment. Using the emulsion droplets formed by the device, a class I ligase ribozyme, bcI 23, was successfully synthesized from DNA attached to magnetic microbeads by 17 RNA polymerase. It was also ligated with an RNA substrate on the same microbeads, and detected using flow cytometry with a fluorescent probe. In addition, a single-chain derivative of the lambda Cro protein was expressed using an Escherichia coli cell-free protein synthesis system in emulsion, which was prepared using the flow-focusing device. In both emulsified reactions, usage of the flow focusing device was able to greatly reduce the coefficient of variation for the amount of RNA or protein displayed on the microbeads, demonstrating the device is advantageous for quantitative analysis in high-throughput screening. (C) 2015, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:471 / 476
页数:6
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