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PMID: 22159718 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ultra high resolution linear ion trap Orbitrap mass spectrometer (Orbitrap Elite) facilitates top down LC MS/MS and versatile peptide fragmentation modes.

Molecular & cellular proteomics : MCP ·Vol. 11 ·No. 3 ·2012-03-00 ·Pages O111.013698

Michalski A, Damoc E, Lange O, Denisov E, Nolting D, Müller M, Viner R, Schwartz J, Remes P, Belford M, Dunyach JJ, Cox J, Horning S, Mann M, Makarov A

Abstract

Although only a few years old, the combination of a linear ion trap with an Orbitrap analyzer has become one of the standard mass spectrometers to characterize proteins and proteomes. Here we describe a novel version of this instrument family, the Orbitrap Elite, which is improved in three main areas. The ion transfer optics has an ion path that blocks the line of sight to achieve more robust operation. The tandem MS acquisition speed of the dual cell linear ion trap now exceeds 12 Hz. Most importantly, the resolving power of the Orbitrap analyzer has been increased twofold for the same transient length by employing a compact, high-field Orbitrap analyzer that almost doubles the observed frequencies. An enhanced Fourier Transform algorithm-incorporating phase information-further doubles the resolving power to 240,000 at m/z 400 for a 768 ms transient. For top-down experiments, we combine a survey scan with a selected ion monitoring scan of the charge state of the protein to be fragmented and with several HCD microscans. Despite the 120,000 resolving power for SIM and HCD scans, the total cycle time is within several seconds and therefore suitable for liquid chromatography tandem MS. For bottom-up proteomics, we combined survey scans at 240,000 resolving power with data-dependent collision-induced dissociation of the 20 most abundant precursors in a total cycle time of 2.5 s-increasing protein identifications in complex mixtures by about 30%. The speed of the Orbitrap Elite furthermore allows scan modes in which complementary dissociation mechanisms are routinely obtained of all fragmented peptides.

MeSH Terms
Chromatography, Liquid HeLa Cells Humans Peptide Fragments/analysis,metabolism Proteome/analysis,metabolism Proteomics/instrumentation,methods Tandem Mass Spectrometry/instrumentation,methods
Chemicals
Peptide Fragments Proteome
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Michalski Annette
Department of Proteomics and Signal Transduction, Max-Planck Institute for Biochemistry, Am Klopferspitz 18, D-82152 Martinsried, Germany.
Damoc Eugen
Lange Oliver
Denisov Eduard
Nolting Dirk
Müller Mathias
Viner Rosa
Schwartz Jae
Remes Philip
Belford Michael
Dunyach Jean-Jacques
Cox Juergen
Horning Stevan
Mann Matthias
Makarov Alexander
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Article Info
Journal
Molecular & cellular proteomics : MCP
Abbr.
Mol Cell Proteomics
ISSN
1535-9484
Published
2012-03-00
Epub
2011-00-09
Pages
O111.013698
Language
English
Region
United States
NLM ID
101125647
PMCID
PMC3316736
Subset
IM
Analysis Services
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