Microfluidic approaches for systems and synthetic biology

被引:44
|
作者
Szita, Nicolas [1 ]
Polizzi, Karen [2 ,3 ]
Jaccard, Nicolas [1 ,4 ]
Baganz, Frank [1 ]
机构
[1] UCL, Dept Biochem Engn, London WC1E 7JE, England
[2] Univ London Imperial Coll Sci Technol & Med, Ctr Synthet Biol & Innovat, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Div Mol Biosci, London SW7 2AZ, England
[4] UCL, Ctr Math & Phys Life Sci & Expt Biol, London WC1E 6BT, England
基金
英国工程与自然科学研究理事会;
关键词
SINGLE-CELL; MASS-SPECTROMETRY; EXPRESSION; DEVICE; CHIP; MICROBIOREACTOR; MICROCHEMOSTAT; MICROCHIP; PROTEINS; DROPLETS;
D O I
10.1016/j.copbio.2010.08.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microfluidic systems miniaturise biological experimentation leading to reduced sample volume, analysis time and cost. Recent innovations have allowed the application of -omics approaches on the microfluidic scale. It is now possible to perform 1.5 million PCR reactions simultaneously, obtain transcriptomic data from as little as 150 cells (as few as 2 transcripts per gene of interest) and perform mass-spectrometric analyses online. For synthetic biology, unit operations have been developed that allow de novo construction of synthetic systems from oligonucleotide synthesis through to high-throughput, high efficiency electroporation of single cells or encapsulation into abiotic chassis enabling the processing of thousands of synthetic organisms per hour. Future directions include a push towards integrating more processes into a single device and replacing off-chip analyses where possible.
引用
收藏
页码:517 / 523
页数:7
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