Environmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Biological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Anal Chem. 2019 Oct 15;91(20):13119-13127. doi: 10.1021/acs.analchem.9b03349. Epub 2019 Sep 25.
Effective extension of mass spectrometry-based proteomics to single cells remains challenging. Herein we combined microfluidic nanodroplet technology with tandem mass tag (TMT) isobaric labeling to significantly improve analysis throughput and proteome coverage for single mammalian cells. Isobaric labeling facilitated multiplex analysis of single cell-sized protein quantities to a depth of ∼1 600 proteins with a median CV of 10.9% and correlation coefficient of 0.98. To demonstrate in-depth high throughput single cell analysis, the platform was applied to measure protein expression in 72 single cells from three murine cell populations (epithelial, immune, and endothelial cells) in <2 days instrument time with over 2 300 proteins identified. Principal component analysis grouped the single cells into three distinct populations based on protein expression with each population characterized by well-known cell-type specific markers. Our platform enables high throughput and unbiased characterization of single cell heterogeneity at the proteome level.
基于质谱的蛋白质组学向单细胞的有效扩展仍然具有挑战性。在此,我们将微流控纳升液滴技术与串联质量标签(TMT)同量异位标记相结合,显著提高了单个哺乳动物细胞的分析通量和蛋白质组覆盖率。同量异位标记有助于对单细胞大小的蛋白质数量进行多重分析,深度可达约 1600 种蛋白质,中位数 CV 为 10.9%,相关系数为 0.98。为了证明深度高通量单细胞分析,该平台在不到 2 天的仪器时间内应用于测量来自三种鼠类细胞群(上皮细胞、免疫细胞和内皮细胞)的 72 个单细胞中的蛋白质表达,鉴定了超过 2300 种蛋白质。主成分分析根据蛋白质表达将单细胞分为三个不同的群体,每个群体都具有特征性的细胞类型特异性标志物。我们的平台能够在蛋白质组水平上高通量且无偏地对单细胞异质性进行表征。