Revealing new biology from multiplexed, metal-isotope-tagged, single-cell readouts

Mass cytometry (MC) is a recent technology that pairs plasma-based ionization of cells in suspension with time-of-flight (TOF) mass spectrometry to sensitively quantify the single-cell abundance of metal-isotope-tagged affinity reagents to key proteins, RNA, and peptides. Given the ability to multiplex readouts (~50 per cell) and capture millions of cells per experiment, MC offers a robust way to assay rare, transitional cell states that are pertinent to human development and disease. Here, we review MC approaches that let us probe the dynamics of cellular regulation across multiple conditions and sample types in a single experiment. Additionally, we discuss current limitations and future extensions of MC as well as computational tools commonly used to extract biological insight from single-cell proteomic datasets.

Automated summary

Mass cytometry is a recent technology that allows sensitive quantification of the single-cell abundance of metal-isotope-tagged affinity reagents to key proteins, RNA, and peptides. It offers a robust way to analyze the dynamics of cellular regulation across multiple conditions and sample types in a single experiment.