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Single-Cell Chemical Lysis Method for Analyses of Intracellular Molecules Using an Array of Picoliter-Scale Microwells

机译:单细胞化学裂解法分析使用微升级微孔阵列的细胞内分子

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摘要

Analyzing the intracellular contents and enzymatic activities of single cells is important for studying the physiological and pathological activities at the cellular level. For this purpose, we developed a simple single-cell lysis method by using a dense array of microwells of 10-30-pL volume fabricated by poly(dimethylsiloxane) (PDMS) and a commercially available cell lysis reagent. To demonstrate the performance of this single-cell lysis method, we carried out two different assays at the single-cell level: detection of proteins by antibody conjugated microbeads and measurement of protease activity by fluorescent substrates. The results indicated that this method readily enabled us to monitor protein levels and enzymatic activities in a single cell. Because this method required only an array of PDMS microwells and a fluorescence microscope, the simplicity of this platform opens a way to explore the biochemical characteristics of single cells even by those who are not familiar with microfluidic technology.
机译:分析单细胞的细胞内含量和酶活性对于研究细胞水平上的生理和病理活性很重要。为此,我们开发了一种简单的单细胞裂解方法,方法是使用由聚二甲基硅氧烷(PDMS)和市售细胞裂解试剂制成的10-30 pL体积的微孔密集阵列。为了证明这种单细胞裂解方法的性能,我们在单细胞水平上进行了两种不同的测定:通过抗体结合的微珠检测蛋白质,并通过荧光底物测量蛋白酶活性。结果表明,该方法使我们能够轻松监测单个细胞中的蛋白质水平和酶活性。由于此方法仅需要一组PDMS微孔和荧光显微镜,因此该平台的简单性为了解单个细胞的生化特征提供了一种途径,即使是不熟悉微流体技术的人也可以使用。

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