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Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood
Theoretical distribution of isoelectric points (pI values) of human blood proteins exhibits multi-modality with a deep minimum in the range between pI 7.30 and 7.50. Considering that the pH of human blood is 7.4±0.1, normal forms of human proteins tend to eschew this specific pI region, thus avoidin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Applied Systems srl
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159840/ https://www.ncbi.nlm.nih.gov/pubmed/32309586 http://dx.doi.org/10.15190/d.2016.14 |
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author | Pirmoradian, Mohammad Aarsland, Dag Zubarev, Roman A. |
author_facet | Pirmoradian, Mohammad Aarsland, Dag Zubarev, Roman A. |
author_sort | Pirmoradian, Mohammad |
collection | PubMed |
description | Theoretical distribution of isoelectric points (pI values) of human blood proteins exhibits multi-modality with a deep minimum in the range between pI 7.30 and 7.50. Considering that the pH of human blood is 7.4±0.1, normal forms of human proteins tend to eschew this specific pI region, thus avoiding charge neutrality that can result in enhanced precipitation. However, abnormal protein isoforms (proteoforms), which are the hallmarks and potential biomarkers of certain diseases, are likely to be found everywhere in the pI distribution, including this “forbidden” region. Therefore, we hypothesized that damaging proteoforms characteristic for neurodegenerative diseases are best detected around pI≈7.4. Blood serum samples from 14 Alzheimer's disease patients were isolated by capillary isoelectric focusing and analyzed by liquid chromatography hyphenated with tandem mass spectrometry. Consistent with the pI≈7.4 hypothesis, the 8 patients with fast memory decline had a significantly (p<0.003) higher concentration of proteoforms in the pI=7.4±0.1 region than the 6 patients with a slow memory decline. Moreover, protein compositions differed more from each other than for any other investigated pI region, providing absolute separation of the fast and slow decliner samples. The discovery of the “treasure island” of abnormal proteoforms in form of the pI≈7.4 region promises to boost biomarker development for a range of diseases. |
format | Online Article Text |
id | pubmed-7159840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Applied Systems srl |
record_format | MEDLINE/PubMed |
spelling | pubmed-71598402020-04-17 Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood Pirmoradian, Mohammad Aarsland, Dag Zubarev, Roman A. Discoveries (Craiova) Original Article Theoretical distribution of isoelectric points (pI values) of human blood proteins exhibits multi-modality with a deep minimum in the range between pI 7.30 and 7.50. Considering that the pH of human blood is 7.4±0.1, normal forms of human proteins tend to eschew this specific pI region, thus avoiding charge neutrality that can result in enhanced precipitation. However, abnormal protein isoforms (proteoforms), which are the hallmarks and potential biomarkers of certain diseases, are likely to be found everywhere in the pI distribution, including this “forbidden” region. Therefore, we hypothesized that damaging proteoforms characteristic for neurodegenerative diseases are best detected around pI≈7.4. Blood serum samples from 14 Alzheimer's disease patients were isolated by capillary isoelectric focusing and analyzed by liquid chromatography hyphenated with tandem mass spectrometry. Consistent with the pI≈7.4 hypothesis, the 8 patients with fast memory decline had a significantly (p<0.003) higher concentration of proteoforms in the pI=7.4±0.1 region than the 6 patients with a slow memory decline. Moreover, protein compositions differed more from each other than for any other investigated pI region, providing absolute separation of the fast and slow decliner samples. The discovery of the “treasure island” of abnormal proteoforms in form of the pI≈7.4 region promises to boost biomarker development for a range of diseases. Applied Systems srl 2016-12-01 /pmc/articles/PMC7159840/ /pubmed/32309586 http://dx.doi.org/10.15190/d.2016.14 Text en Copyright: © 2016, Pirmoradian et al. and Applied Systems http://creativecommons.org/licenses/by/4.0/ This article 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 work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Article Pirmoradian, Mohammad Aarsland, Dag Zubarev, Roman A. Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title | Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title_full | Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title_fullStr | Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title_full_unstemmed | Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title_short | Isoelectric point region pI≈7.4 as a treasure island of abnormal proteoforms in blood |
title_sort | isoelectric point region pi≈7.4 as a treasure island of abnormal proteoforms in blood |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159840/ https://www.ncbi.nlm.nih.gov/pubmed/32309586 http://dx.doi.org/10.15190/d.2016.14 |
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