| Title | Analysis of Tandem Mass Spectra by FTMS for Improved Large-Scale Proteomics with Superior Protein Quantification |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | McAlister, GC, Phanstiel, D, Wenger, CD, Lee, VM, Coon, JJ |
| Journal | Analytical Chemistry |
| Volume | 82 |
| Pagination | 316-322 |
| Date Published | Jan |
| Accession Number | ISI:000273265700050 |
| Keywords | accurate mass, amino-acid sequences, Chemistry, Analytical, electron-transfer dissociation, high-resolution, identification, Linear ion-trap, peptide mixtures, quantitative-analysis, search algorithm, spectrometry |
| Abstract | Using a newly developed dual-cell quadrupole linear ion trap-orbitrap hybrid mass spectrometer (dcQLT-orbitrap), we demonstrate the utility of collecting high-resolution tandem mass spectral data for large-scale shotgun proteomics. Multiple nanoLC-MS/MS experiments on both an older generation quadrupole linear ion trap-orbitrap hybrid (QLT-orbitrap) and the dcQLT-orbitrap, using both resonant-excitation CAD and beam-type CAD (HCD), were performed. Resulting from various technological advances (e.g., a stacked ring ion guide AP inlet, a dual cell QLT), the dcQLT-orbitrap exhibited increased duty cycle (similar to 1.5-2 times) and sensitivity for both CAD (ion trap detection) and HCD (orbitrap detection) methods. As compared to the older system, the dcQLT-orbitrap produced significantly more unique peptide identifications for both methods (similar to 30% improvement for CAD and similar to 115% improvement for HCD). The sizable improvement of the HCD method on the dcQLT-orbitrap system outperforms the current standard method of CAD with ion trap detection for large-scale analysis. Finally, we demonstrate that the increased HCD performance translates to a direct and substantial improvement in protein quantitation precision using isobaric tags. |
| Short Title | Anal. Chem |