Abstract
Spatially resolved mass spectrometry-based proteomics at single-cell resolution promises to provide insights into biological heterogeneity. We describe a protocol based on multiplexed data-independent acquisition (mDIA) with dimethyl labeling to enhance proteome depth, accuracy, and throughput while minimizing costs. It enables high-quality proteome analysis of single isolated hepatocytes and utilizes liver zonation for single-cell proteomics benchmarking. This adaptable, modular protocol will promote the use of single-cell proteomics in spatial biology.
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Thielert, M., Weiss, C. A. M., Mann, M., & Rosenberger, F. A. (2024). Spatial Proteomics of Single Hepatocytes with Multiplexed Data-Independent Acquisition (mDIA). Methods in Molecular Biology (Clifton, N.J.), 2817, 97–113. https://doi.org/10.1007/978-1-0716-3934-4_9
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