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bioRxiv · 10.1101/2025.10.27.684859

SPIN: Inkjet-Driven Nanowell Workflow for Scalable and Sensitive Single-Cell Proteomics

Cheng, E.·Chi, S.·Zhong, H.·Coope, R.·Foster, L. J.·Cheung, K. C.
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Abstract

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 sealed 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 a near 100% protein completeness detected among the enzymes in the Kreb cycle in both A549 and astrocytes, suggesting the consistency across all samples evaluated. This platform addresses core processing bottlenecks and enables reliable, scalable single-cell proteomics.

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Cheng, E., Chi, S., Zhong, H., Coope, R., Foster, L. J., Cheung, K. C.. 2025-10-28. SPIN: Inkjet-Driven Nanowell Workflow for Scalable and Sensitive Single-Cell Proteomics. https://doi.org/10.1101/2025.10.27.684859

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