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Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein
The serum protein α(1)-acid glycoprotein (AGP), also known as orosomucoid, is generally described as an archetypical positive acute phase protein. Here, porcine AGP was identified, purified and characterized from pooled pig serum. It was found to circulate as a single chain glycoprotein having an ap...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699587/ https://www.ncbi.nlm.nih.gov/pubmed/23844161 http://dx.doi.org/10.1371/journal.pone.0068110 |
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author | Heegaard, Peter M. H. Miller, Ingrid Sorensen, Nanna Skall Soerensen, Karen Elisabeth Skovgaard, Kerstin |
author_facet | Heegaard, Peter M. H. Miller, Ingrid Sorensen, Nanna Skall Soerensen, Karen Elisabeth Skovgaard, Kerstin |
author_sort | Heegaard, Peter M. H. |
collection | PubMed |
description | The serum protein α(1)-acid glycoprotein (AGP), also known as orosomucoid, is generally described as an archetypical positive acute phase protein. Here, porcine AGP was identified, purified and characterized from pooled pig serum. It was found to circulate as a single chain glycoprotein having an apparent molecular weight of 43 kDa by SDS-PAGE under reducing conditions, of which approximately 17 kDa were accounted for by N-bound oligosaccharides. Those data correspond well with the properties of the protein predicted from the single porcine AGP gene (ORM1, Q29014 (UniProt)), containing 5 putative glycosylation sites. A monoclonal antibody (MAb) was produced and shown to quantitatively and specifically react with all microheterogenous forms of pig AGP as analyzed by 2-D electrophoresis. This MAb was used to develop an immunoassay (ELISA) for quantification of AGP in pig serum samples. The adult serum concentrations of pig AGP were in the range of 1–3 mg/ml in a number of conventional pig breeds while it was lower in Göttingen and Ossabaw minipigs (in the 0.3 to 0.6 mg/ml range) and higher in young (2–5 days old) conventional pigs (mean: 6.6 mg/ml). Surprisingly, pig AGP was found to behave as a negative acute phase protein during a range of experimental infections and aseptic inflammation with significant decreases in serum concentration and in hepatic ORM1 expression during the acute phase response. To our knowledge this is the first description in any species of AGP being a negative acute phase protein. |
format | Online Article Text |
id | pubmed-3699587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36995872013-07-10 Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein Heegaard, Peter M. H. Miller, Ingrid Sorensen, Nanna Skall Soerensen, Karen Elisabeth Skovgaard, Kerstin PLoS One Research Article The serum protein α(1)-acid glycoprotein (AGP), also known as orosomucoid, is generally described as an archetypical positive acute phase protein. Here, porcine AGP was identified, purified and characterized from pooled pig serum. It was found to circulate as a single chain glycoprotein having an apparent molecular weight of 43 kDa by SDS-PAGE under reducing conditions, of which approximately 17 kDa were accounted for by N-bound oligosaccharides. Those data correspond well with the properties of the protein predicted from the single porcine AGP gene (ORM1, Q29014 (UniProt)), containing 5 putative glycosylation sites. A monoclonal antibody (MAb) was produced and shown to quantitatively and specifically react with all microheterogenous forms of pig AGP as analyzed by 2-D electrophoresis. This MAb was used to develop an immunoassay (ELISA) for quantification of AGP in pig serum samples. The adult serum concentrations of pig AGP were in the range of 1–3 mg/ml in a number of conventional pig breeds while it was lower in Göttingen and Ossabaw minipigs (in the 0.3 to 0.6 mg/ml range) and higher in young (2–5 days old) conventional pigs (mean: 6.6 mg/ml). Surprisingly, pig AGP was found to behave as a negative acute phase protein during a range of experimental infections and aseptic inflammation with significant decreases in serum concentration and in hepatic ORM1 expression during the acute phase response. To our knowledge this is the first description in any species of AGP being a negative acute phase protein. Public Library of Science 2013-07-02 /pmc/articles/PMC3699587/ /pubmed/23844161 http://dx.doi.org/10.1371/journal.pone.0068110 Text en © 2013 Heegaard et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Heegaard, Peter M. H. Miller, Ingrid Sorensen, Nanna Skall Soerensen, Karen Elisabeth Skovgaard, Kerstin Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title | Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title_full | Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title_fullStr | Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title_full_unstemmed | Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title_short | Pig α(1)-Acid Glycoprotein: Characterization and First Description in Any Species as a Negative Acute Phase Protein |
title_sort | pig α(1)-acid glycoprotein: characterization and first description in any species as a negative acute phase protein |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699587/ https://www.ncbi.nlm.nih.gov/pubmed/23844161 http://dx.doi.org/10.1371/journal.pone.0068110 |
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