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Identification of autoantigens in body fluids by combining pull-downs and organic precipitations of intact immune complexes with quantitative label-free mass spectrometry.
J. Proteome Res. 12, 5656-5665 (2013)
Most autoimmune diseases are multifactorial diseases and are caused by the immunological reaction against a number of autoantigens. Key for understanding autoimmune pathologies is the knowledge of the targeted autoantigens, both initially and during disease progression. We present an approach for autoantigen identification based on isolation of intact autoantibody-antigen complexes from body fluids. After organic precipitation of high molecular weight proteins and free immunoglobulins, released autoantigens were identified by quantitative label-free liquid chromatography mass spectrometry. We confirmed feasibility of target enrichment and identification from highly complex body fluid proteomes by spiking of a pre-defined antigen-antibody complex at low level of abundance. As a proof of principle we studied the blinding disease autoimmune uveitis, which is caused by autoreactive T-cells attacking the inner eye and is accompanied by autoantibodies. We identified three novel autoantigens in the spontaneous animal model equine recurrent uveitis (secreted acidic phosphoprotein osteopontin, extracellular matrix protein 1 and metalloproteinase inhibitor 2) and confirmed presence of the corresponding autoantibodies in 15 - 25% of patient samples by enzyme-linked immunosorbent assay. Thus, this workflow led to the identification of novel autoantigens in autoimmune uveitis and may provide a versatile and useful tool to identify autoantigens in other autoimmune diseases in future.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Altmetric
5.056
1.312
13
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Autoantibody ; Autoantigen ; Autoimmune Uveitis ; Label-free Mass Spectrometry ; Progenesis Lc-ms ; Acetonitrile Precipitation; Equine Recurrent Uveitis ; Multiple-sclerosis ; Cerebrospinal-fluid ; Autoimmune Uveitis ; S-antigen ; Tissue Inhibitor ; Human Serum ; Proteins ; Osteopontin ; Expression
Sprache
englisch
Veröffentlichungsjahr
2013
HGF-Berichtsjahr
2013
ISSN (print) / ISBN
1535-3893
e-ISSN
1535-3907
Zeitschrift
Journal of Proteome Research
Quellenangaben
Band: 12,
Heft: 12,
Seiten: 5656-5665
Verlag
American Chemical Society (ACS)
Verlagsort
Washington
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
PubMed ID
24059262
WOS ID
WOS:000328231300027
Scopus ID
84890017699
Erfassungsdatum
2013-10-01