| Literature DB >> 31509397 |
Maowei Dou1, Geremy Clair2, Chia-Feng Tsai2, Kerui Xu1, William B Chrisler2, Ryan L Sontag2, Rui Zhao1, Ronald J Moore2, Tao Liu2, Ljiljana Pasa-Tolic1, Richard D Smith2, Tujin Shi2, Joshua N Adkins2, Wei-Jun Qian2, Ryan T Kelly1,3, Charles Ansong2, Ying Zhu1.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31509397 PMCID: PMC7192326 DOI: 10.1021/acs.analchem.9b03349
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986