4.8 Article

High-Throughput Single Cell Proteomics Enabled by Multiplex Isobaric Labeling in a Nanodroplet Sample Preparation Platform

Journal

ANALYTICAL CHEMISTRY
Volume 91, Issue 20, Pages 13119-13127

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.9b03349

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Funding

  1. Laboratory Directed Research and Development award from Pacific Northwest National Laboratory (PNNL) [UC4 DK108101, U01 HL122703, R21 CA223715, R33 CA225248, DP3 DK110844, U24CA210955, P41 GM103493]
  2. IARPA FunGCAT Program [166156]
  3. Department of Energy (DOE) [DE-AC05-76RL0 1830]

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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 similar to 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.

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