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Selection and characterisation of Affimers specific for CEA recognition
Carcinoembryonic antigen (CEA) is the only blood based protein biomarker at present, used for preoperative screening of advanced colorectal cancer (CRC) patients to determine the appropriate curative treatments and post-surveillance screening for tumour recurrence. Current diagnostics for CRC detect...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804248/ https://www.ncbi.nlm.nih.gov/pubmed/33436840 http://dx.doi.org/10.1038/s41598-020-80354-6 |
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author | Shamsuddin, Shazana Hilda Jayne, David G. Tomlinson, Darren C. McPherson, Michael J. Millner, Paul A. |
author_facet | Shamsuddin, Shazana Hilda Jayne, David G. Tomlinson, Darren C. McPherson, Michael J. Millner, Paul A. |
author_sort | Shamsuddin, Shazana Hilda |
collection | PubMed |
description | Carcinoembryonic antigen (CEA) is the only blood based protein biomarker at present, used for preoperative screening of advanced colorectal cancer (CRC) patients to determine the appropriate curative treatments and post-surveillance screening for tumour recurrence. Current diagnostics for CRC detection have several limitations and development of a highly sensitive, specific and rapid diagnostic device is required. The majority of such devices developed to date are antibody-based and suffer from shortcomings including multimeric binding, cost and difficulties in mass production. To circumvent antibody-derived limitations, the present study focused on the development of Affimer proteins as a novel alternative binding reagent for CEA detection. Here, we describe the selection, from a phage display library, of Affimers specific to CEA protein. Characterization of three anti-CEA Affimers reveal that these bind specifically and selectively to protein epitopes of CEA from cell culture lysate and on fixed cells. Kinetic binding analysis by SPR show that the Affimers bind to CEA with high affinity and within the nM range. Therefore, they have substantial potential for used as novel affinity reagents in diagnostic imaging, targeted CRC therapy, affinity purification and biosensor applications. |
format | Online Article Text |
id | pubmed-7804248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78042482021-01-13 Selection and characterisation of Affimers specific for CEA recognition Shamsuddin, Shazana Hilda Jayne, David G. Tomlinson, Darren C. McPherson, Michael J. Millner, Paul A. Sci Rep Article Carcinoembryonic antigen (CEA) is the only blood based protein biomarker at present, used for preoperative screening of advanced colorectal cancer (CRC) patients to determine the appropriate curative treatments and post-surveillance screening for tumour recurrence. Current diagnostics for CRC detection have several limitations and development of a highly sensitive, specific and rapid diagnostic device is required. The majority of such devices developed to date are antibody-based and suffer from shortcomings including multimeric binding, cost and difficulties in mass production. To circumvent antibody-derived limitations, the present study focused on the development of Affimer proteins as a novel alternative binding reagent for CEA detection. Here, we describe the selection, from a phage display library, of Affimers specific to CEA protein. Characterization of three anti-CEA Affimers reveal that these bind specifically and selectively to protein epitopes of CEA from cell culture lysate and on fixed cells. Kinetic binding analysis by SPR show that the Affimers bind to CEA with high affinity and within the nM range. Therefore, they have substantial potential for used as novel affinity reagents in diagnostic imaging, targeted CRC therapy, affinity purification and biosensor applications. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804248/ /pubmed/33436840 http://dx.doi.org/10.1038/s41598-020-80354-6 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 Shamsuddin, Shazana Hilda Jayne, David G. Tomlinson, Darren C. McPherson, Michael J. Millner, Paul A. Selection and characterisation of Affimers specific for CEA recognition |
title | Selection and characterisation of Affimers specific for CEA recognition |
title_full | Selection and characterisation of Affimers specific for CEA recognition |
title_fullStr | Selection and characterisation of Affimers specific for CEA recognition |
title_full_unstemmed | Selection and characterisation of Affimers specific for CEA recognition |
title_short | Selection and characterisation of Affimers specific for CEA recognition |
title_sort | selection and characterisation of affimers specific for cea recognition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804248/ https://www.ncbi.nlm.nih.gov/pubmed/33436840 http://dx.doi.org/10.1038/s41598-020-80354-6 |
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