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用于实时配制试剂及其随后包封成双乳液的微流控装置。

Microfluidic device for real-time formulation of reagents and their subsequent encapsulation into double emulsions.

机构信息

Institute of Materials, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

出版信息

Sci Rep. 2018 May 25;8(1):8143. doi: 10.1038/s41598-018-26542-x.

Abstract

Emulsion drops are often employed as picoliter-sized containers to perform screening assays. These assays usually entail the formation of drops encompassing discrete objects such as cells or microparticles and reagents to study interactions between the different encapsulants. Drops are also used to screen influences of reagent concentrations on the final product. However, these latter assays are less frequently performed because it is difficult to change the reagent concentration over a wide range and with high precision within a single experiment. In this paper, we present a microfluidic double emulsion drop maker containing pneumatic valves that enable real-time formulation of different reagents using pulse width modulation and consequent encapsulation of the mixed solutions. This device can produce drops from reagent volumes as low as 10 µL with minimal sample loss, thereby enabling experiments that would be prohibitively expensive using drop generators that do not contain valves. We employ this device to monitor the kinetics of the cell-free synthesis of green fluorescent proteins inside double emulsions. To demonstrate the potential of this device for real-time formulation, we perform DNA titration experiments to test the influence of DNA concentration on the amount of green fluorescence protein produced in double emulsions by a coupled cell-free transcription / translation system.

摘要

乳液滴通常被用作皮升级别的容器来进行筛选分析。这些分析通常需要形成包含离散物体(如细胞或微颗粒)和试剂的液滴,以研究不同包封剂之间的相互作用。液滴也用于筛选试剂浓度对最终产物的影响。然而,由于很难在单个实验中高精度地大范围改变试剂浓度,因此这些后续分析的应用较少。在本文中,我们提出了一种含有气动阀的微流控双乳液滴生成器,它可以使用脉冲宽度调制实时配置不同的试剂,并随后封装混合溶液。该设备可以从低至 10 μL 的试剂体积中生成液滴,而样品损失最小,从而能够进行使用不含阀门的液滴生成器会非常昂贵的实验。我们使用该设备来监测无细胞合成绿色荧光蛋白在双乳液中的动力学。为了展示该设备实时配方的潜力,我们进行了 DNA 滴定实验,以测试 DNA 浓度对耦合无细胞转录/翻译系统在双乳液中产生的绿色荧光蛋白量的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b75/5970246/dd2c1f5b1d4b/41598_2018_26542_Fig1_HTML.jpg

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