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Nat Commun ; 13(1): 37, 2022 01 10.
Article in English | MEDLINE | ID: mdl-35013269

ABSTRACT

Single-cell proteomics can reveal cellular phenotypic heterogeneity and cell-specific functional networks underlying biological processes. Here, we present a streamlined workflow combining microfluidic chips for all-in-one proteomic sample preparation and data-independent acquisition (DIA) mass spectrometry (MS) for proteomic analysis down to the single-cell level. The proteomics chips enable multiplexed and automated cell isolation/counting/imaging and sample processing in a single device. Combining chip-based sample handling with DIA-MS using project-specific mass spectral libraries, we profile on average ~1,500 protein groups across 20 single mammalian cells. Applying the chip-DIA workflow to profile the proteomes of adherent and non-adherent malignant cells, we cover a dynamic range of 5 orders of magnitude with good reproducibility and <16% missing values between runs. Taken together, the chip-DIA workflow offers all-in-one cell characterization, analytical sensitivity and robustness, and the option to add additional functionalities in the future, thus providing a basis for advanced single-cell proteomics applications.


Subject(s)
Lab-On-A-Chip Devices , Mass Spectrometry/methods , Microfluidics/methods , Proteomics/methods , Animals , Cell Line, Tumor , Cell Separation , Humans , Lung Neoplasms , Proteome , Reproducibility of Results , Workflow
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