Huang Lu, Michael Sean A, Chen Yangfan, Wu Hongkai
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.
Chem Asian J. 2017 Jul 18;12(14):1680-1691. doi: 10.1002/asia.201700404. Epub 2017 Jun 13.
Single-cell measurements have played a critical role in revealing the complex signaling dynamics and heterogeneity present in cells, but there is still much to learn. Measuring samples from bulk populations of cells often masks the information and dynamics present in subsets of cells. Common single-cell protein studies rely on fluorescent microscopy and flow cytometry but are limited in multiplexing ability owing to spectral overlap. Recently, technology advancements in single-cell proteomics have allowed highly multiplexed measurement of multiple parameters simultaneously by using barcoded microfluidic enzyme-linked immunosorbent assays and mass cytometry techniques. In this review, we will describe recent work around multiparameter single-cell protein measurements and critically analyze the techniques.
单细胞测量在揭示细胞中存在的复杂信号动态和异质性方面发挥了关键作用,但仍有许多有待了解的地方。对大量细胞群体的样本进行测量往往会掩盖细胞亚群中存在的信息和动态。常见的单细胞蛋白质研究依赖于荧光显微镜和流式细胞术,但由于光谱重叠,其多重检测能力有限。最近,单细胞蛋白质组学的技术进步使得通过使用条形码微流控酶联免疫吸附测定和质谱细胞术技术能够同时对多个参数进行高度多重检测。在这篇综述中,我们将描述围绕多参数单细胞蛋白质测量的近期工作,并对这些技术进行批判性分析。