ArticleJournal of the American Society for Mass Spectrometry2006
High amplitude short time excitation: a method to form and detect low mass product ions in a quadrupole ion trap mass spectrometer.
Article in Journal of the American Society for Mass Spectrometry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
22 citing papers in PubMed.
- Quantitative Assessment of Six Different Reagent Gases for Charge Transfer Dissociation (CTD) of Biological Ions.International journal of mass spectrometry · 2021Article
- Identification of small molecules using accurate mass MS/MS search.Mass spectrometry reviews · 2018Review
- Multigenerational Broadband Collision-Induced Dissociation of Precursor Ions in a Linear Quadrupole Ion Trap.Journal of the American Society for Mass Spectrometry · 2016Article
- Theoretical Study of Dual-Direction Dipolar Excitation of Ions in Linear Ion Traps.Journal of the American Society for Mass Spectrometry · 2016Article
- Ion sponge: a 3-dimentional array of quadrupole ion traps for trapping and mass-selectively processing ions in gas phase.Analytical chemistry · 2014Article
- Implementation of dipolar resonant excitation for collision induced dissociation with ion mobility/time-of-flight MS.Journal of the American Society for Mass Spectrometry · 2014Article
- Covalent labeling with isotopically encoded reagents for faster structural analysis of proteins by mass spectrometry.Analytical chemistry · 2013Article
- Protein analysis by shotgun/bottom-up proteomics.Chemical reviews · 2013Review
- iTRAQ labeling is superior to mTRAQ for quantitative global proteomics and phosphoproteomics.Molecular & cellular proteomics : MCP · 2012Article
- Infrared multiphoton dissociation for quantitative shotgun proteomics.Analytical chemistry · 2012Article
- Tandem mass spectrometry identifies many mouse brain O-GlcNAcylated proteins including EGF domain-specific O-GlcNAc transferase targets.Proceedings of the National Academy of Sciences of the United States of America · 2012Article
- Identification of proteins and phosphoproteins using pulsed Q collision induced dissociation (PQD).Journal of the American Society for Mass Spectrometry · 2011Article
- Quantification of tryptic peptides in quadrupole ion trap using high-mass signals derived from isotope-coded N-acetyl dipeptide tags.Journal of the American Society for Mass Spectrometry · 2011Article
- Adaptation of a 3-D quadrupole ion trap for dipolar DC collisional activation.Journal of the American Society for Mass Spectrometry · 2011Article
- A novel two-stage tandem mass spectrometry approach and scoring scheme for the identification of O-GlcNAc modified peptides.Journal of the American Society for Mass Spectrometry · 2011Article
- Proteomic analysis of a noninvasive human model of acute inflammation and its resolution: the twenty-one day gingivitis model.Journal of proteome research · 2010Article
- Infrared multiphoton dissociation of peptide cations in a dual pressure linear ion trap mass spectrometer.Analytical chemistry · 2009Article
- Combined pulsed-Q dissociation and electron transfer dissociation for identification and quantification of iTRAQ-labeled phosphopeptides.Analytical chemistry · 2009Article
- Off-resonance excitation in a linear ion trap.Journal of the American Society for Mass Spectrometry · 2009Article
- Robust and sensitive iTRAQ quantification on an LTQ Orbitrap mass spectrometer.Molecular & cellular proteomics : MCP · 2008Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Collision induced dissociation (CID) in a quadrupole ion trap mass spectrometer using the conventional 30 ms activation time is compared with high amplitude short time excitation (HASTE) CID using 2 ms and 1 ms activation times. As a result of the shorter activation times, dissociation of the parent ions using the HASTE CID technique requires resonance excitation voltages greater than conventional CID. After activation, the rf trapping voltage is lowered to allow product ions below the low mass cut-off to be trapped. The HASTE CID spectra are notably different from those obtained using conventional CID and can include product ions below the low mass cut-off for the parent ions of interest. The MS/MS efficiencies of HASTE CID are not significantly different when compared with the conventional 30 ms CID. Similar results were obtained with a two-dimensional (linear) ion trap and a three-dimensional ion trap.
Identifiers
16352436What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.