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Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1
Specific and selective anti-CB(1) antibodies are among the most powerful research tools to unravel the complex biological processes mediated by the CB(1) receptor in both physiological and pathological conditions. However, low performance of antibodies remains a major source of inconsistency between...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604870/ https://www.ncbi.nlm.nih.gov/pubmed/34453219 http://dx.doi.org/10.1007/s00418-021-02025-5 |
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author | Echeazarra, Leyre García del Caño, Gontzal Barrondo, Sergio González-Burguera, Imanol Saumell-Esnaola, Miquel Aretxabala, Xabier López de Jesús, Maider Borrega-Román, Leire Mato, Susana Ledent, Catherine Matute, Carlos Goicolea, María Aranzazu Sallés, Joan |
author_facet | Echeazarra, Leyre García del Caño, Gontzal Barrondo, Sergio González-Burguera, Imanol Saumell-Esnaola, Miquel Aretxabala, Xabier López de Jesús, Maider Borrega-Román, Leire Mato, Susana Ledent, Catherine Matute, Carlos Goicolea, María Aranzazu Sallés, Joan |
author_sort | Echeazarra, Leyre |
collection | PubMed |
description | Specific and selective anti-CB(1) antibodies are among the most powerful research tools to unravel the complex biological processes mediated by the CB(1) receptor in both physiological and pathological conditions. However, low performance of antibodies remains a major source of inconsistency between results from different laboratories. Using a variety of techniques, including some of the most commonly accepted ones for antibody specificity testing, we identified three of five commercial antibodies against different regions of CB(1) receptor as the best choice for specific end-use purposes. Specifically, an antibody against a long fragment of the extracellular amino tail of CB(1) receptor (but not one against a short sequence of the extreme amino-terminus) detected strong surface staining when applied to live cells, whereas two different antibodies against an identical fragment of the extreme carboxy-terminus of CB(1) receptor (but not one against an upstream peptide) showed acceptable performance on all platforms, although they behaved differently in immunohistochemical assays depending on the tissue fixation procedure used and showed different specificity in Western blot assays, which made each of them particularly suitable for one of those techniques. Our results provide a framework to interpret past and future results derived from the use of different anti-CB(1) antibodies in the context of current knowledge about the CB(1) receptor at the molecular level, and highlight the need for an adequate validation for specific purposes, not only before antibodies are placed on the market, but also before the decision to discontinue them is made. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00418-021-02025-5. |
format | Online Article Text |
id | pubmed-8604870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-86048702021-12-03 Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 Echeazarra, Leyre García del Caño, Gontzal Barrondo, Sergio González-Burguera, Imanol Saumell-Esnaola, Miquel Aretxabala, Xabier López de Jesús, Maider Borrega-Román, Leire Mato, Susana Ledent, Catherine Matute, Carlos Goicolea, María Aranzazu Sallés, Joan Histochem Cell Biol Original Paper Specific and selective anti-CB(1) antibodies are among the most powerful research tools to unravel the complex biological processes mediated by the CB(1) receptor in both physiological and pathological conditions. However, low performance of antibodies remains a major source of inconsistency between results from different laboratories. Using a variety of techniques, including some of the most commonly accepted ones for antibody specificity testing, we identified three of five commercial antibodies against different regions of CB(1) receptor as the best choice for specific end-use purposes. Specifically, an antibody against a long fragment of the extracellular amino tail of CB(1) receptor (but not one against a short sequence of the extreme amino-terminus) detected strong surface staining when applied to live cells, whereas two different antibodies against an identical fragment of the extreme carboxy-terminus of CB(1) receptor (but not one against an upstream peptide) showed acceptable performance on all platforms, although they behaved differently in immunohistochemical assays depending on the tissue fixation procedure used and showed different specificity in Western blot assays, which made each of them particularly suitable for one of those techniques. Our results provide a framework to interpret past and future results derived from the use of different anti-CB(1) antibodies in the context of current knowledge about the CB(1) receptor at the molecular level, and highlight the need for an adequate validation for specific purposes, not only before antibodies are placed on the market, but also before the decision to discontinue them is made. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00418-021-02025-5. Springer Berlin Heidelberg 2021-08-27 2021 /pmc/articles/PMC8604870/ /pubmed/34453219 http://dx.doi.org/10.1007/s00418-021-02025-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Echeazarra, Leyre García del Caño, Gontzal Barrondo, Sergio González-Burguera, Imanol Saumell-Esnaola, Miquel Aretxabala, Xabier López de Jesús, Maider Borrega-Román, Leire Mato, Susana Ledent, Catherine Matute, Carlos Goicolea, María Aranzazu Sallés, Joan Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title | Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title_full | Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title_fullStr | Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title_full_unstemmed | Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title_short | Fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
title_sort | fit-for-purpose based testing and validation of antibodies to amino- and carboxy-terminal domains of cannabinoid receptor 1 |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604870/ https://www.ncbi.nlm.nih.gov/pubmed/34453219 http://dx.doi.org/10.1007/s00418-021-02025-5 |
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