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Kardell, O. ; von Toerne, C. ; Merl-Pham, J. ; König, A.-C. ; Blindert, M. ; Barth, T.K.* ; Mergner, J.* ; Ludwig, C.* ; Tüshaus, J.* ; Eckert, S.* ; Müller, S.A.* ; Breimann, S.* ; Giesbertz, P.* ; Bernhardt, A.M.J.* ; Schweizer, L.* ; Albrecht, V.* ; Teupser, D.* ; Imhof, A.* ; Kuster, B.* ; Lichtenthaler, S.F.* ; Mann, M.* ; Cox, J.* ; Hauck, S.M.

Multicenter collaborative study to optimize mass spectrometry workflows of clinical specimens.

J. Proteome Res. 23, 117-129 (2023)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
The foundation for integrating mass spectrometry (MS)-based proteomics into systems medicine is the development of standardized start-to-finish and fit-for-purpose workflows for clinical specimens. An essential step in this pursuit is to highlight the common ground in a diverse landscape of different sample preparation techniques and liquid chromatography-mass spectrometry (LC-MS) setups. With the aim to benchmark and improve the current best practices among the proteomics MS laboratories of the CLINSPECT-M consortium, we performed two consecutive round-robin studies with full freedom to operate in terms of sample preparation and MS measurements. The six study partners were provided with two clinically relevant sample matrices: plasma and cerebrospinal fluid (CSF). In the first round, each laboratory applied their current best practice protocol for the respective matrix. Based on the achieved results and following a transparent exchange of all lab-specific protocols within the consortium, each laboratory could advance their methods before measuring the same samples in the second acquisition round. Both time points are compared with respect to identifications (IDs), data completeness, and precision, as well as reproducibility. As a result, the individual performances of participating study centers were improved in the second measurement, emphasizing the effect and importance of the expert-driven exchange of best practices for direct practical improvements.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Csf ; Lc–ms ; R Package Mpwr ; Clinical Specimen ; Data-dependent Acquisition ; Data-independent Acquisition ; Interlaboratory ; Intralaboratory ; Mass Spectrometry ; Plasma ; Round-robin Study; Data-independent Acquisition; Proteomics; Quality
Sprache englisch
Veröffentlichungsjahr 2023
HGF-Berichtsjahr 2023
ISSN (print) / ISBN 1535-3893
e-ISSN 1535-3907
Zeitschrift Journal of Proteome Research
Quellenangaben Band: 23, Heft: 1, Seiten: 117-129 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Verlagsort 1155 16th St, Nw, Washington, Dc 20036 Usa
Begutachtungsstatus Peer reviewed
Institut(e) CF Metabolomics & Proteomics (CF-MPC)
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-505700-001
A-630700-001
Förderungen Deutsche Forschungsgemeinschaft(DFG, German Research Foundation)
German Ministry for Science and Education
DOI 10.1021/acs.jproteome.3c00473
WOS ID 001137609000001
Scopus ID 85179612212
PubMed ID 38015820
Erfassungsdatum 2023-12-18
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