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YCharOS open antibody characterisation data: Lessons learned and progress made

YCharOS is a collaborative initiative aimed at characterising antibodies against the entire human proteome. As of August 2023, they have presented comprehensive knockout characterisation data for 812 antibodies and 78 proteins using techniques such as Western blot, immunoprecipitation, and immunoflu...

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Autores principales: Biddle, Michael S., Virk, Harvinder S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579855/
https://www.ncbi.nlm.nih.gov/pubmed/37854875
http://dx.doi.org/10.12688/f1000research.141719.1
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author Biddle, Michael S.
Virk, Harvinder S.
author_facet Biddle, Michael S.
Virk, Harvinder S.
author_sort Biddle, Michael S.
collection PubMed
description YCharOS is a collaborative initiative aimed at characterising antibodies against the entire human proteome. As of August 2023, they have presented comprehensive knockout characterisation data for 812 antibodies and 78 proteins using techniques such as Western blot, immunoprecipitation, and immunofluorescence. YCharOS consolidates its data into reports (one protein per report) available on Zenodo, a public repository controlled by CERN, to ensure open access. To enhance the visibility of their work, the group is progressively converting their Zenodo reports into F1000 articles, collected on the YCharOS Gateway, and indexed via PubMed. Their data is also accessible through searches on the Antibody Registry. The provided data is a valuable resource for researchers when selecting antibodies for specific applications, although certain limitations should be considered. The data accumulated thus far has illuminated the extent of the problem when poorly performing antibodies are employed in research. While the scientific community was already aware that this was likely a widespread issue, the establishment of a collaborative open science project with industry partners introduces an innovative solution that holds the potential to yield significant returns on investment in the public interest. This potential is substantiated by the number of antibodies that have either been withdrawn or had their recommended usage altered by the vendor. However, despite the discovery of high-performing renewable antibodies for most of the studied proteins, this accounts for a tiny fraction of the human proteome and the commercial antibody market. To realise the full potential of this work, end-users must adjust their antibody procurement and usage practises in line with the provided data. This editorial offers a guide on how individual scientists can utilise the YCharOS data, in addition to sharing the insights gained from the data thus far with the wider scientific community.
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spelling pubmed-105798552023-10-18 YCharOS open antibody characterisation data: Lessons learned and progress made Biddle, Michael S. Virk, Harvinder S. F1000Res Editorial YCharOS is a collaborative initiative aimed at characterising antibodies against the entire human proteome. As of August 2023, they have presented comprehensive knockout characterisation data for 812 antibodies and 78 proteins using techniques such as Western blot, immunoprecipitation, and immunofluorescence. YCharOS consolidates its data into reports (one protein per report) available on Zenodo, a public repository controlled by CERN, to ensure open access. To enhance the visibility of their work, the group is progressively converting their Zenodo reports into F1000 articles, collected on the YCharOS Gateway, and indexed via PubMed. Their data is also accessible through searches on the Antibody Registry. The provided data is a valuable resource for researchers when selecting antibodies for specific applications, although certain limitations should be considered. The data accumulated thus far has illuminated the extent of the problem when poorly performing antibodies are employed in research. While the scientific community was already aware that this was likely a widespread issue, the establishment of a collaborative open science project with industry partners introduces an innovative solution that holds the potential to yield significant returns on investment in the public interest. This potential is substantiated by the number of antibodies that have either been withdrawn or had their recommended usage altered by the vendor. However, despite the discovery of high-performing renewable antibodies for most of the studied proteins, this accounts for a tiny fraction of the human proteome and the commercial antibody market. To realise the full potential of this work, end-users must adjust their antibody procurement and usage practises in line with the provided data. This editorial offers a guide on how individual scientists can utilise the YCharOS data, in addition to sharing the insights gained from the data thus far with the wider scientific community. F1000 Research Limited 2023-10-16 /pmc/articles/PMC10579855/ /pubmed/37854875 http://dx.doi.org/10.12688/f1000research.141719.1 Text en Copyright: © 2023 Biddle MS and Virk HS https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editorial
Biddle, Michael S.
Virk, Harvinder S.
YCharOS open antibody characterisation data: Lessons learned and progress made
title YCharOS open antibody characterisation data: Lessons learned and progress made
title_full YCharOS open antibody characterisation data: Lessons learned and progress made
title_fullStr YCharOS open antibody characterisation data: Lessons learned and progress made
title_full_unstemmed YCharOS open antibody characterisation data: Lessons learned and progress made
title_short YCharOS open antibody characterisation data: Lessons learned and progress made
title_sort ycharos open antibody characterisation data: lessons learned and progress made
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579855/
https://www.ncbi.nlm.nih.gov/pubmed/37854875
http://dx.doi.org/10.12688/f1000research.141719.1
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