Molecular & Cellular Proteomics· 2018Q1
Online Parallel Accumulation–Serial Fragmentation (PASEF) with a Novel Trapped Ion Mobility Mass Spectrometer
- 1,046citations
- Q1SCImago
- 2018year
Short summary
The timsTOF Pro instrument, featuring an orthogonal ion path, enables online Parallel Accumulation–Serial Fragmentation (PASEF) for shotgun proteomics, achieving over 6,000 protein identifications in 120 min LC runs and over 2,500 in 30 min runs with only 10 ng of digest.
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Key points
- The timsTOF Pro instrument implements online PASEF with an orthogonal ion path for robustness.
- Over 100 fragmentation events per second are achievable, leading to >6,000 protein IDs in 120 min LC runs.
- High sensitivity is demonstrated with >2,500 protein IDs in 30 min runs using 10 ng HeLa digest.
- Highly reproducible collisional cross-section data (R > 0.99) can be acquired on a large scale.
AI-generated from the title and abstract; the full text is not read.
Abstract
, PMID: 26538118). Here we introduce the timsTOF Pro instrument, which optimally implements online PASEF. It features an orthogonal ion path into the ion mobility device, limiting the amount of debris entering the instrument and making it very robust in daily operation. We investigate different precursor selection schemes for shotgun proteomics to optimally allocate in excess of 100 fragmentation events per second. More than 600,000 fragmentation spectra in standard 120 min LC runs are achievable, which can be used for near exhaustive precursor selection in complex mixtures or accumulating the signal of weak precursors. In 120 min single runs of HeLa digest, MaxQuant identified more than 6,000 proteins without matching to a library and with high quantitative reproducibility (R > 0.97). Online PASEF achieves a remarkable sensitivity with more than 2,500 proteins identified in 30 min runs of only 10 ng HeLa digest. We also show that highly reproducible collisional cross sections can be acquired on a large scale (R > 0.99). PASEF on the timsTOF Pro is a valuable addition to the technological toolbox in proteomics, with a number of unique operating modes that are only beginning to be explored.
The authors' abstract, as published at the source. Molecular & Cellular Proteomics, 2018 · DOI ↗
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Field: Spectroscopy
SpectroscopyChemistry