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Droplet-based microfluidic analysis and screening of single plant cells

机译:基于液滴的微流控分析和单个植物细胞的筛选

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摘要

Droplet-based microfluidics has been used to facilitate high-throughput analysis of individual prokaryote and mammalian cells. However, there is a scarcity of similar workflows applicable to rapid phenotyping of plant systems where phenotyping analyses typically are time-consuming and low-throughput. We report on-chip encapsulation and analysis of protoplasts isolated from the emergent plant model Marchantia polymorpha at processing rates of >100,000 cells per hour. We use our microfluidic system to quantify the stochastic properties of a heat-inducible promoter across a population of transgenic protoplasts to demonstrate its potential for assessing gene expression activity in response to environmental conditions. We further demonstrate on-chip sorting of droplets containing YFP-expressing protoplasts from wild type cells using dielectrophoresis force. This work opens the door to droplet-based microfluidic analysis of plant cells for applications ranging from high-throughput characterisation of DNA parts to single-cell genomics to selection of rare plant phenotypes.
机译:基于液滴的微流体技术已被用于促进单个原核生物和哺乳动物细胞的高通量分析。但是,缺乏适用于植物系统快速表型分析的相似工作流程,其中表型分析通常是耗时且低通量的。我们报告了芯片封装和原生质体分析从新兴的植物模型马钱氏菌多形体中以每小时> 100,000个细胞的处理速度分离。我们使用我们的微流控系统来量化整个基因组原生质体中热诱导型启动子的随机特性,以证明其潜在的潜力来评估响应环境条件的基因表达活性。我们进一步证明了使用介电泳力从野生型细胞中包含表达YFP原生质体的液滴的片上分选。这项工作为基于液滴的植物细胞微流体分析打开了大门,其应用范围从DNA部件的高通量表征到单细胞基因组学到稀有植物表型的选择。

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