Profiling the Proteome of Exhaled Breath Condensate in Healthy Smokers and COPD Patients by LC-MS/MS
Authors:
- Marco FumagalliMFMarco Fumagalli
- Fabio FerrariFFFabio Ferrari
- Maurizio LuisettiMLMaurizio Luisetti
- Jan StolkJSJan Stolk
- Pieter S. HiemstraPHPieter S. Hiemstra
- Daniela CapuanoDCDaniela Capuano
- Simona ViglioSVSimona Viglio
- Laura FregoneseLFLaura Fregonese
- Isa CerveriICIsa Cerveri
- Federica CoranaFCFederica Corana
- Carmine TinelliCTCarmine Tinelli
- Paolo IadarolaPaolo Iadarola
Open Access
- 29 October 2012
- journal article
- research article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 13 (11) , 13894-13910
Abstract
Three pools of exhaled breath condensate (EBC) from non-smokers plus healthy smokers (NS + HS, n = 45); chronic obstructive pulmonary disease (COPD) without emphysema (COPD, n = 15) and subjects with pulmonary emphysema associated with α1-antitrypsin deficiency (AATD, n = 23) were used for an exploratory proteomic study aimed at generating fingerprints of these groups that can be used in future pathophysiological and perhaps even clinical research. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was the platform applied for this hypothesis-free investigation. Analysis of pooled specimens resulted in the production of a “fingerprint” made of 44 proteins for NS/HS; 17 for COPD and 15 for the group of AATD subjects. Several inflammatory cytokines (IL-1α, IL-1β, IL-2; IL-12, α and β subunits, IL-15, interferon α and γ, tumor necrosis factor α); Type I and II cytokeratins; two SP-A isoforms; Calgranulin A and B and α1-antitrypsin were detected and validated through the use of surface enhanced laser-desorption ionization mass spectrometry (SELDI-MS) and/or by Western blot (WB) analysis. These results are the prelude of quantitative studies aimed at identifying which of these proteins hold promise as identifiers of differences that could distinguish healthy subjects from patients.Keywords
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