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Cyclic microchip assay for measurement of hundreds of functional proteins in single neurons

  • Liwei Yang
  • , Avery Ball
  • , Jesse Liu
  • , Tanya Jain
  • , Yue Ming Li
  • , Firoz Akhter
  • , Donghui Zhu
  • , Jun Wang
  • Stony Brook University
  • Memorial Sloan-Kettering Cancer Center
  • Cornell University

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Despite the fact that proteins carry out nearly all cellular functions and mark the differences of cells, the existing single-cell tools can only analyze dozens of proteins, a scale far from full characterization of cells and tissue yet. Herein, we present a single-cell cyclic multiplex in situ tagging (CycMIST) technology that affords the comprehensive functional proteome profiling of single cells. We demonstrate the technology by detecting 182 proteins that include surface markers, neuron function proteins, neurodegeneration markers, signaling pathway proteins, and transcription factors. Further studies on cells derived from the 5XFAD mice, an Alzheimer’s Disease (AD) model, validate the utility of our technology and reveal the deep heterogeneity of brain cells. Through comparison with control mouse cells, we have identified differentially expressed proteins in AD pathology. Our technology could offer new insights into cell machinery and thus may advance many fields including drug discovery, molecular diagnostics, and clinical studies.

Original languageEnglish
Article number3548
JournalNature Communications
Volume13
Issue number1
DOIs
StatePublished - Dec 2022

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