PuSH - Publikationsserver des Helmholtz Zentrums München

Apoe, Mbl2 and Psp plasma protein levels correlate with diabetic phenotype in NZO mice - an optimized rapid workflow for SRM-based quantification.

J. Proteome Res. 12, 1331-1343 (2013)
Verlagsversion Volltext DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Male New Zealand Obese (NZO) mice progress through pathophysiological stages similar to humans developing obesity-associated type 2 diabetes (T2D). The current challenge is to establish quantitative proteomics from small plasma sample amounts. We established an analytical workflow that facilitates a reproducible depletion of high-abundance proteins, has high throughput applicability, and allows absolute quantification of proteins from mouse plasma samples by LC-SRM-MS. The ProteoMiner equalizing technology was adjusted to the small sample amount and reproducibility of the identifications was monitored by spike proteins. Based on the label-free relative quantification of proteins in depleted plasma of a test set of NZO mice, assays for potential candidates were designed for the setup of a targeted selected reaction monitoring (SRM) approach and absolute quantification. We could demonstrate that apolipoprotein E (Apoe), mannose-binding lectin 2 (Mbl2) and parotid secretory protein (Psp) are present at significantly different quantities in depleted plasma of diabetic NZO mice compared to non-diabetic controls using AQUA peptides. Quantification was validated for Mbl2 using the ELISA technology on non-depleted plasma. We conclude that the depletion technique is applicable to restricted sample amounts and suitable for the identification of T2D signatures in plasma.
Altmetric
Weitere Metriken?
Tags
PROT-CF
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Type 2 Diabetes ; New Zealand Obese Mouse ; Proteominer ; Depletion ; Label-free Quantification ; Selected Reaction Monitoring ; Absolute Quantification ; Aqua Peptides ; Protein Signatures; New-zealand Obese ; Mannose-binding Lectin ; Parotid Secretory Protein ; Peptide Ligand Libraries ; Apolipoprotein-e ; Metabolic Syndrome ; Cell Destruction ; Innate Immunity ; Dietary-fat ; Mouse Model
ISSN (print) / ISBN 1535-3893
e-ISSN 1535-3907
Quellenangaben Band: 12, Heft: 3, Seiten: 1331-1343 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Begutachtungsstatus Peer reviewed