Robust, reproducible and quantitative analysis of thousands of proteomes by micro-flow LC-MS/MS.
Yangyang BianRunsheng ZhengFlorian P BayerCassandra WongYun-Chien ChangChen MengDaniel P ZolgMaria ReineckeJana ZechaSvenja WiechmannStephanie HeinzlmeirJohannes ScherrBernhard HemmerMike BaynhamAnne-Claude GingrasOleksandr BoychenkoBernhard KusterPublished in: Nature communications (2020)
Nano-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.
Keyphrases
- protein protein
- liquid chromatography tandem mass spectrometry
- small molecule
- simultaneous determination
- solid phase extraction
- endothelial cells
- genome wide
- gene expression
- magnetic resonance imaging
- magnetic resonance
- ms ms
- emergency department
- binding protein
- high resolution
- mass spectrometry
- electronic health record
- artificial intelligence
- deep learning
- drug induced
- label free
- pluripotent stem cells