Robust, reproducible and quantitative analysis of thousands of proteomes by micro-flow LC–MS/MS

Author:

Bian Yangyang,Zheng Runsheng,Bayer Florian P.,Wong Cassandra,Chang Yun-Chien,Meng Chen,Zolg Daniel P.,Reinecke Maria,Zecha JanaORCID,Wiechmann SvenjaORCID,Heinzlmeir Stephanie,Scherr Johannes,Hemmer BernhardORCID,Baynham Mike,Gingras Anne-ClaudeORCID,Boychenko Oleksandr,Kuster BernhardORCID

Abstract

AbstractNano-flow liquid chromatography tandem mass spectrometry (nano-flow LC–MS/MS) is the mainstay in proteome research because of its excellent sensitivity but often comes at the expense of robustness. Here we show that micro-flow LC–MS/MS using a 1 × 150 mm column shows excellent reproducibility of chromatographic retention time (<0.3% coefficient of variation, CV) and protein quantification (<7.5% CV) using data from >2000 samples of human cell lines, tissues and body fluids. Deep proteome analysis identifies >9000 proteins and >120,000 peptides in 16 h and sample multiplexing using tandem mass tags increases throughput to 11 proteomes in 16 h. The system identifies >30,000 phosphopeptides in 12 h and protein-protein or protein-drug interaction experiments can be analyzed in 20 min per sample. We show that the same column can be used to analyze >7500 samples without apparent loss of performance. This study demonstrates that micro-flow LC–MS/MS is suitable for a broad range of proteomic applications.

Funder

National Natural Science Foundation of China

Alexander von Humboldt-Stiftung

Deutsche Forschungsgemeinschaft

Bundesministerium für Bildung und Forschung

Gouvernement du Canada | Canadian Institutes of Health Research

Ontario Genomics Institute

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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