Sollid Ludvig M LM

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Proteomics (4)

Organisms

Alphavirus (2)
Anemia (2)
Archaea (2)
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Betaherpesvirinae (2)
Borrelia (2)
Clostridium perfringens (2)
Cowpox virus (2)
Cytomegalovirus (2)
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EFO:0001352 (2)
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Miscanthus x giganteus (2)
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Severe acute respiratory syndrome coronavirus 2 (2)
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MassIVE (2)
pride (2)

Tissue

Blood serum (1)
Small intestine (1)

Disease

Celiac disease (2)

Technology Type

Mass Spectrometry (2)
Shotgun proteomics (2)

Instrument Platform

Q Exactive (2)

Publication Date

2017 (2)
2019 (1)
2018 (1)

Lab affiliation

KG Jebsen Coeliac Disease Research Centre, University of Oslo, 0372 Oslo, Norway (1)
KG Jebsen Coeliac Disease Research Centre, University of Oslo, NO-0372 Oslo, Norway (1)

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Characterization of the small intestinal lesion in celiac disease by label-free quantitative mass spectrometry

This study describes a comparison of global proteome expression in small intestinal tissue collected from celiac disease patients at different stages of disease. We have analyzed sections from FFPE biopsy blocks and identified more than 4500 protein without sample pre-fractionation. We have compared...

ORGANISM(S): Homo sapiens (Human)

2018-11-21 | PXD008992 | Pride

Immunoglobulin V-gene usage among human serum IgA with or without specificity to the autoantigen transglutaminase 2

To study V-gene usage among antigen-specific and non-antigen-specific serum IgA antibodies in celiac disease patients, purified antibody fractions were subjected to proteomic analysis. Patients either had eastablished, untreated disease with severe intestinal inflammation or "potential" celiac disea...

ORGANISM(S): Homo sapiens (Human)

2019-07-09 | PXD013777 | Pride

Human Serum Autoantibodies Iga Celiac disease

Gluten-specific antibodies of celiac disease gut plasma cells recognize long proteolytic fragments that typically harbor T-cell epitopes

This study aimed to identify proteolytic fragments of gluten proteins recognized by recombinant IgG1 monoclonal antibodies generated from single IgA plasma cells of celiac disease lesions. Peptides bound by monoclonal antibodies in complex gut-enzyme digests of gluten treated with the deamidating en...

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

2017-03-29 | MSV000080779 | MassIVE

Different Binding Motifs of the Celiac Disease Associated HLA Molecules DQ2.5, DQ2.2 and DQ7.5 Revealed by Relative Quantitative Proteomics of Endogenous Peptide Repertoires

In this study relative quantitative analysis of endogenous peptides by mass spectrometry combined with neural network analysis have been used to address why the alpha- or beta-chain sharing human leukocyte antigen (HLA)-DQ molecules DQ2.5, DQ2.2 and DQ7.5 display different risks for celiac disease. ...