Identification of human tear fluid biomarkers in vernal keratoconjunctivitis using iTRAQ quantitative proteomics. Issue 2 (13th December 2013)
- Record Type:
- Journal Article
- Title:
- Identification of human tear fluid biomarkers in vernal keratoconjunctivitis using iTRAQ quantitative proteomics. Issue 2 (13th December 2013)
- Main Title:
- Identification of human tear fluid biomarkers in vernal keratoconjunctivitis using iTRAQ quantitative proteomics
- Authors:
- Leonardi, A.
Palmigiano, A.
Mazzola, E. A.
Messina, A.
Milazzo, E. M. S.
Bortolotti, M.
Garozzo, D. - Abstract:
- <abstract abstract-type="main" id="all12331-abs-0001"> <title>Abstract</title> <sec id="all12331-sec-0001" sec-type="section"> <title>Background</title> <p>Understanding and treating vernal keratoconjunctivitis (VKC) has been a challenge because the pathogenesis is unclear and antiallergic therapy often unsuccessful. The aim of the study was to analyze peptide profiles in human tears using mass spectrometry to elucidate compositional differences between healthy subjects and patients affected by VKC.</p> </sec> <sec id="all12331-sec-0002" sec-type="section"> <title>Methods</title> <p>Tears were collected from healthy subjects and VKC patients. Digested samples were treated with iTRAQ (isobaric tag for relative and absolute quantitation). Separation of tryptic peptides was realized using a MicroHPLC interfaced with a microfraction collector. MS and MS/MS mass spectra were performed using a MALDI TOF/TOF 4800 Applied Biosystem spectrometer. Protein Pilot™ software with Paragon™ algorithm v4.1.46 or GPS™ with Mascot engine was used as search engines with SwissProt or IPI human as the databases.</p> </sec> <sec id="all12331-sec-0003" sec-type="section"> <title>Results</title> <p>A significant number of peptides were examined, and 78 proteins were successfully identified. In all VKC samples, levels of serum albumin, transferrin, and hemopexin were found up to 100 times higher than control tear levels and correlated to the severity of disease. Hemopexin, transferrin, mammaglobin B,<abstract abstract-type="main" id="all12331-abs-0001"> <title>Abstract</title> <sec id="all12331-sec-0001" sec-type="section"> <title>Background</title> <p>Understanding and treating vernal keratoconjunctivitis (VKC) has been a challenge because the pathogenesis is unclear and antiallergic therapy often unsuccessful. The aim of the study was to analyze peptide profiles in human tears using mass spectrometry to elucidate compositional differences between healthy subjects and patients affected by VKC.</p> </sec> <sec id="all12331-sec-0002" sec-type="section"> <title>Methods</title> <p>Tears were collected from healthy subjects and VKC patients. Digested samples were treated with iTRAQ (isobaric tag for relative and absolute quantitation). Separation of tryptic peptides was realized using a MicroHPLC interfaced with a microfraction collector. MS and MS/MS mass spectra were performed using a MALDI TOF/TOF 4800 Applied Biosystem spectrometer. Protein Pilot™ software with Paragon™ algorithm v4.1.46 or GPS™ with Mascot engine was used as search engines with SwissProt or IPI human as the databases.</p> </sec> <sec id="all12331-sec-0003" sec-type="section"> <title>Results</title> <p>A significant number of peptides were examined, and 78 proteins were successfully identified. In all VKC samples, levels of serum albumin, transferrin, and hemopexin were found up to 100 times higher than control tear levels and correlated to the severity of disease. Hemopexin, transferrin, mammaglobin B, and secretoglobin 1D were found significantly over‐expressed in VKC samples compared with the control samples. Tear samples from patients treated with topical cyclosporine or corticosteroids showed a dramatic reduction in these protein levels.</p> </sec> <sec id="all12331-sec-0004" sec-type="section"> <title>Conclusions</title> <p>LC MALDI MS and isobaric tag for relative and absolute quantitation technique may be useful in the quantitative and qualitative characterization of the peptidoma of human tears. These techniques may identify target proteins to be used in the diagnosis and management of VKC and other inflammatory ocular surface conditions.</p> </sec> </abstract> … (more)
- Is Part Of:
- Allergy. Volume 69:Issue 2(2014:Feb.)
- Journal:
- Allergy
- Issue:
- Volume 69:Issue 2(2014:Feb.)
- Issue Display:
- Volume 69, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 69
- Issue:
- 2
- Issue Sort Value:
- 2014-0069-0002-0000
- Page Start:
- 254
- Page End:
- 260
- Publication Date:
- 2013-12-13
- Subjects:
- Allergy -- Periodicals
616.97 - Journal URLs:
- http://estar.bl.uk/cgi-bin/sciserv.pl?collection=journals&journal=01054538 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1398-9995 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/all.12331 ↗
- Languages:
- English
- ISSNs:
- 0105-4538
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0790.945000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3251.xml