Simple Targeted Assays for Metabolic Pathways and Signaling: A Powerful Tool for Targeted Proteomics
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Simple Targeted Assays for Metabolic Pathways and Signaling: A Powerful Tool for Targeted Proteomics. / Kopczynski, Dominik; Hentschel, Andreas; Coman, Cristina; Schebb, Nils Helge; Hornemann, Thorsten; Mashek, Douglas G; Hartung, Nicole M; Shevchuk, Olga; Schött, Hans-Frieder; Lorenz, Kristina; Torta, Federico; Burla, Bo; Zahedi, René P; Sickmann, Albert; Kreutz, Michael R; Ejsing, Christer S; Medenbach, Jan; Ahrends, Robert.
in: ANAL CHEM, Jahrgang 92, Nr. 20, 20.10.2020, S. 13672-13676.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Simple Targeted Assays for Metabolic Pathways and Signaling: A Powerful Tool for Targeted Proteomics
AU - Kopczynski, Dominik
AU - Hentschel, Andreas
AU - Coman, Cristina
AU - Schebb, Nils Helge
AU - Hornemann, Thorsten
AU - Mashek, Douglas G
AU - Hartung, Nicole M
AU - Shevchuk, Olga
AU - Schött, Hans-Frieder
AU - Lorenz, Kristina
AU - Torta, Federico
AU - Burla, Bo
AU - Zahedi, René P
AU - Sickmann, Albert
AU - Kreutz, Michael R
AU - Ejsing, Christer S
AU - Medenbach, Jan
AU - Ahrends, Robert
PY - 2020/10/20
Y1 - 2020/10/20
N2 - We introduce STAMPS, a pathway-centric web service for the development of targeted proteomics assays. STAMPS guides the user by providing several intuitive interfaces for a rapid and simplified method design. Applying our curated framework to signaling and metabolic pathways, we reduced the average assay development time by a factor of ∼150 and revealed that the insulin signaling is actively controlled by protein abundance changes in insulin-sensitive and -resistance states. Although at the current state STAMPS primarily contains mouse data, it was designed for easy extension with additional organisms.
AB - We introduce STAMPS, a pathway-centric web service for the development of targeted proteomics assays. STAMPS guides the user by providing several intuitive interfaces for a rapid and simplified method design. Applying our curated framework to signaling and metabolic pathways, we reduced the average assay development time by a factor of ∼150 and revealed that the insulin signaling is actively controlled by protein abundance changes in insulin-sensitive and -resistance states. Although at the current state STAMPS primarily contains mouse data, it was designed for easy extension with additional organisms.
U2 - 10.1021/acs.analchem.0c02793
DO - 10.1021/acs.analchem.0c02793
M3 - SCORING: Journal article
C2 - 32865986
VL - 92
SP - 13672
EP - 13676
JO - ANAL CHEM
JF - ANAL CHEM
SN - 0003-2700
IS - 20
ER -