Abstract
Modern proteomics requires reagents for exact quantification of peptides in complex mixtures. Peptide labelling is most typically achieved with isobaric tags that consist of a balancer and a reporter part that separate in the gas phase. An ingenious distribution of stable isotopes provides multiple reagents with identical molecular weight but a different mass of the reporter groups, allowing relative quantification of multiple samples in one measurement. Current generation reagents require a high fragmentation energy for cleavage, leading to incomplete fragmentation and hence loss of signal intensity. Here we report a new isobaric labelling reagent, where the balancer and the reporter are linked by a sulfoxide group, which, based on the sulfoxide pyrolysis, leads to easy and asymmetric cleavage at low fragmentation energy. The fragmentation of our new design is significantly improved, yielding more intense complementary ion signals, allowing complementary ion cluster analysis as well.
Dokumententyp: | Zeitschriftenartikel |
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EU Funded Grant Agreement Number: | 642023 |
EU-Projekte: | Horizon 2020 > Marie Skłodowska Curie Actions > Marie Skłodowska-Curie Innovative Training Networks > 642023: ClickGene - Click Chemistry for Future Gene Therapies to Benefit Citizens, Researchers and Industry |
Publikationsform: | Postprint |
Keywords: | Peptide derivatization reagent; sulfoxide pyrolysis; isobaric labelling; quantitative mass spectrometry; complementary ion clusters; proteomics |
Fakultät: | Chemie und Pharmazie > Department Chemie |
Fakultätsübergreifende Einrichtungen: | Center for Integrated Protein Science Munich (CIPSM) |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 540 Chemie
500 Naturwissenschaften und Mathematik > 570 Biowissenschaften; Biologie |
URN: | urn:nbn:de:bvb:19-epub-60591-5 |
ISSN: | 1433-7851 |
Sprache: | Englisch |
Dokumenten ID: | 60591 |
Datum der Veröffentlichung auf Open Access LMU: | 14. Feb. 2019, 09:29 |
Letzte Änderungen: | 04. Nov. 2020, 13:38 |