IceR improves proteome coverage and data completeness in global and single-cell proteomics

Mathias Kalxdorf (), Torsten Müller, Oliver Stegle and Jeroen Krijgsveld ()
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Mathias Kalxdorf: German Cancer Research Center
Torsten Müller: German Cancer Research Center
Oliver Stegle: German Cancer Research Center
Jeroen Krijgsveld: German Cancer Research Center

Nature Communications, 2021, vol. 12, issue 1, 1-15

Abstract: Abstract Label-free proteomics by data-dependent acquisition enables the unbiased quantification of thousands of proteins, however it notoriously suffers from high rates of missing values, thus prohibiting consistent protein quantification across large sample cohorts. To solve this, we here present IceR (Ion current extraction Re-quantification), an efficient and user-friendly quantification workflow that combines high identification rates of data-dependent acquisition with low missing value rates similar to data-independent acquisition. Specifically, IceR uses ion current information for a hybrid peptide identification propagation approach with superior quantification precision, accuracy, reliability and data completeness compared to other quantitative workflows. Applied to plasma and single-cell proteomics data, IceR enhanced the number of reliably quantified proteins, improved discriminability between single-cell populations, and allowed reconstruction of a developmental trajectory. IceR will be useful to improve performance of large scale global as well as low-input proteomics applications, facilitated by its availability as an easy-to-use R-package.

Date: 2021
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DOI: 10.1038/s41467-021-25077-6

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