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Lipid-Coated Microdroplet Array for in Vitro Protein Synthesis

机译:脂质包裹的微滴阵列用于体外蛋白质合成

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Monitoring complex biological assays such as in vitro protein synthesis over long periods in micrometer-sized cavities of poly(dimethyl siloxane) (PDMS) microfluidic devices requires a strategy that solves the adsorption and absorption problems on PDMS surfaces. In this study, we developed a technique that instantaneously arrays aqueous microdroplets coated with a phospholipid membrane within a single microfluidic device. The simple lipid bilayer coating effectively inhibits the adsorption of proteins and DNA, whereas the encapsulation of the droplet reduces the area in contact with the PDMS surface, resulting in decreased absorption in part. Although the size becomes smaller during the first few hours, a lipid-coated microdroplet array demonstrated a temporal stability of more than 20 h and a size uniformity of CV 3percent in the device. Furthermore, we succeeded in expressing a green fluorescent protein by confining an in vitro translation system in the microdroplets, which was confirmed by scanning the fluorescence spectrum of the droplets, demonstrating that the lipid coat secured the synthetic reaction from the adsorption problem.
机译:监测复杂的生物学检测方法,例如在微米大小的聚二甲基硅氧烷(PDMS)微流控设备的腔体中长时间进行体外蛋白质合成,需要一种解决PDMS表面吸附和吸收问题的策略。在这项研究中,我们开发了一种技术,可在单个微流控设备中即时排列涂有磷脂膜的水性微滴。简单的脂质双层涂层有效地抑制了蛋白质和DNA的吸附,而液滴的包裹减少了与PDMS表面接触的面积,从而导致部分吸收降低。尽管在开始的几个小时内尺寸变小,但脂质包裹的微滴阵列在装置中显示出超过20小时的时间稳定性和3%的CV尺寸均匀性。此外,我们通过限制微滴中的体外翻译系统成功表达了绿色荧光蛋白,这通过扫描微滴的荧光光谱得到了证实,表明脂质涂层可确保合成反应免受吸附问题的影响。

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