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Alpha-Synuclein Antibody Characterization: Why Semantics Matters
In protein aggregation disorders, we assume that, during the process of protein aggregation, different types of aggregated species (oligomers, protofibrils, fibrils, etc.) are formed, some of which can be toxic to cells/tissues/organs. Recent evidence from numerous studies in cell and animal models...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018929/ https://www.ncbi.nlm.nih.gov/pubmed/33411246 http://dx.doi.org/10.1007/s12035-020-02269-7 |
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author | Outeiro, Tiago Fleming |
author_facet | Outeiro, Tiago Fleming |
author_sort | Outeiro, Tiago Fleming |
collection | PubMed |
description | In protein aggregation disorders, we assume that, during the process of protein aggregation, different types of aggregated species (oligomers, protofibrils, fibrils, etc.) are formed, some of which can be toxic to cells/tissues/organs. Recent evidence from numerous studies in cell and animal models of disease suggest that oligomeric species of different proteins might be more toxic that the larger, fibrillar forms. However, we still lack definitive data on the nature of the toxic species, mostly due to our inability to detect and define the various protein species that form as protein aggregate. The terms used are often broad and do not capture inter-laboratory variation in protocols and methods used for the characterization of aggregates. Even antibody-based methods can be ambiguous, as antibodies are delicate tools. Therefore, systematic and interdisciplinary studies are essential in order to guide future developments in the field. |
format | Online Article Text |
id | pubmed-8018929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-80189292021-04-16 Alpha-Synuclein Antibody Characterization: Why Semantics Matters Outeiro, Tiago Fleming Mol Neurobiol Article In protein aggregation disorders, we assume that, during the process of protein aggregation, different types of aggregated species (oligomers, protofibrils, fibrils, etc.) are formed, some of which can be toxic to cells/tissues/organs. Recent evidence from numerous studies in cell and animal models of disease suggest that oligomeric species of different proteins might be more toxic that the larger, fibrillar forms. However, we still lack definitive data on the nature of the toxic species, mostly due to our inability to detect and define the various protein species that form as protein aggregate. The terms used are often broad and do not capture inter-laboratory variation in protocols and methods used for the characterization of aggregates. Even antibody-based methods can be ambiguous, as antibodies are delicate tools. Therefore, systematic and interdisciplinary studies are essential in order to guide future developments in the field. Springer US 2021-01-07 2021 /pmc/articles/PMC8018929/ /pubmed/33411246 http://dx.doi.org/10.1007/s12035-020-02269-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Outeiro, Tiago Fleming Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title | Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title_full | Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title_fullStr | Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title_full_unstemmed | Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title_short | Alpha-Synuclein Antibody Characterization: Why Semantics Matters |
title_sort | alpha-synuclein antibody characterization: why semantics matters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018929/ https://www.ncbi.nlm.nih.gov/pubmed/33411246 http://dx.doi.org/10.1007/s12035-020-02269-7 |
work_keys_str_mv | AT outeirotiagofleming alphasynucleinantibodycharacterizationwhysemanticsmatters |