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Updated: Mar 14, 2026

Counting Proteins in Single Cells with Addressable Droplet Microarrays
Published on: July 6, 2018
SPIN: Inkjet-Driven Nanowell Workflow for Scalable and Sensitive Single-Cell Proteomics
Eric Cheng1, Shuxin Chi2, Huan Zhong2
1Department of Electrical and Computer Engineering, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
None:
Single-cell proteomics is emerging as a powerful approach to resolve cellular heterogeneity, yet sample processing remains challenging due to limited input material and the absence of protein amplification. We present a protocol centered on an image-guided, machine-learning-driven inkjet single-cell printer integrated with a dew-point-controlled nanowell chip to reduce loss, increase throughput, and improve reproducibility. The system dispenses single cells at >1 Hz into sealable nanoliter wells with minimal surface contact, virtually eliminating evaporation; a high-thermal-conductivity aluminum substrate and precise environmental control further ensure exceptional reproducibility. Relative to a commercial dispenser, the workflow yields significantly higher protein and peptide recovery without bias toward high-abundance species, delivering uniformly deep coverage. Biological pathway analysis emphasizes the robustness of this workflow, as there is nearly 100% protein completeness detected among the enzymes in the Krebs cycle in both A549 and astrocytes, suggesting consistency across all samples evaluated. This platform addresses core processing bottlenecks and enables reliable, scalable single-cell proteomics.

