4.5 Review

Deep Profiling of Cellular Heterogeneity by Emerging Single-Cell Proteomic Technologies

Journal

PROTEOMICS
Volume 20, Issue 13, Pages -

Publisher

WILEY
DOI: 10.1002/pmic.201900226

Keywords

cellular heterogeneity; DNA barcoded antibodies; mass cytometry; microchips; single cell proteomics

Funding

  1. State University of New York at Stony Brook
  2. National Institute of Health [R01GM12898401]

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The ability to comprehensively profile cellular heterogeneity in functional proteome is crucial in advancing the understanding of cell behavior, organism development, and disease mechanisms. Conventional bulk measurement by averaging the biological responses across a population often loses the information of cellular variations. Single-cell proteomic technologies are becoming increasingly important to understand and discern cellular heterogeneity. The well-established methods for single-cell protein analysis based on flow cytometry and fluorescence microscopy are limited by the low multiplexing ability owing to the spectra overlap of fluorophores for labeling antibodies. Recent advances in mass spectrometry (MS), microchip, and reiterative staining-based techniques for single-cell proteomics have enabled the evaluation of cellular heterogeneity with high throughput, increased multiplexity, and improved sensitivity. In this review, the principles, developments, advantages, and limitations of these advanced technologies in analysis of single-cell proteins, along with their biological applications to study cellular heterogeneity, are described. At last, the remaining challenges, possible strategies, and future opportunities that will facilitate the improvement and broad applications of single-cell proteomic technologies in cell biology and medical research are discussed.

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