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首页> 外文期刊>Journal of biomolecular screening: The official journal of the Society for Biomolecular Screening >High-Throughput Microfluidic Mixing and Multiparametric Cell Sorting for Bioactive Compound Screening
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High-Throughput Microfluidic Mixing and Multiparametric Cell Sorting for Bioactive Compound Screening

机译:高通量微流控混合和多参数细胞分选,用于生物活性化合物的筛选

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摘要

HyperCyt, an automated sample handling system for flow cytometry that uses air bubbles to separate samples sequentially introduced from multiwell plates by an autosampler. In a previously documented HyperCyt configuration, air bubble separated compounds in one sample line and a continuous stream of cells in another are mixed in-line for serial flow cytometric cell response analysis. To expand capabilities for high-throughput bioactive compound screening, the authors investigated using this system configuration in combination with automated cell sorting. Peptide ligands were sampled from a 96-well plate, mixed in-line with fluo-4-loaded, formyl peptide receptor-transfected U937 cells, and screened at a rate of 3 peptide reactions per minute with ~10,000 cells analyzed per reaction. Cell Ca~(2+) responses were detected to as little as 10~(-11) M peptide with no detectable carryover between samples at up to 10~(-7) M peptide. After expansion in culture, cells sort-purified from the 10% highest responders exhibited enhanced sensitivity and more sustained responses to peptide. Thus, a highly responsive cell subset was isolated under high-throughput mixing and sorting conditions in which response detection capability spanned a 1000-fold range of peptide concentration. With single-cell readout systems for protein expression libraries, this technology offers the promise of screening millions of discrete compound interactions per day.
机译:HyperCyt,一种用于流式细胞术的自动化样品处理系统,该系统使用气泡来分离由自动进样器从多孔板依次引入的样品。在先前记录的HyperCyt配置中,将一个样品管线中的气泡分离化合物与另一个样品管线中的连续细胞流进行管线内混合,以进行串行流式细胞术细胞反应分析。为了扩展高通量生物活性化合物筛选的功能,作者研究了将此系统配置与自动细胞分选结合使用的情况。从96孔板中取样肽配体​​,与经fluo-4-加载的甲酰肽受体转染的U937细胞在线混合,并以每分钟3个肽反应的速率进行筛选,每个反应分析约10,000个细胞。检测到细胞Ca〜(2+)响应低至10〜(-11)M肽,样品之间高达10〜(-7)M的肽没有可检测的残留。培养扩增后,从10%最高响应者中分选纯化的细胞表现出增强的敏感性和对肽的更持久响应。因此,在高通量混合和分选条件下分离了高响应性细胞亚群,其中响应检测能力跨越了肽浓度的1000倍范围。借助用于蛋白质表达文库的单细胞读出系统,该技术有望每天筛选数百万个离散的化合物相互作用。

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