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Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX
Alpha-fetoprotein (AFP) is a liver cancer associated protein and has long been utilized as a serum tumor biomarker of disease progression. AFP is usually detected in HCC patients by an antibody based system. Recently, however, aptamers generated from systematic evolution of ligands by exponential en...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620443/ https://www.ncbi.nlm.nih.gov/pubmed/26497223 http://dx.doi.org/10.1038/srep15552 |
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author | Dong, Lili Tan, Qiwen Ye, Wei Liu, Dongli Chen, Haifeng Hu, Hongwei Wen, Duo Liu, Yang Cao, Ya Kang, Jingwu Fan, Jia Guo, Wei Wu, Weizhong |
author_facet | Dong, Lili Tan, Qiwen Ye, Wei Liu, Dongli Chen, Haifeng Hu, Hongwei Wen, Duo Liu, Yang Cao, Ya Kang, Jingwu Fan, Jia Guo, Wei Wu, Weizhong |
author_sort | Dong, Lili |
collection | PubMed |
description | Alpha-fetoprotein (AFP) is a liver cancer associated protein and has long been utilized as a serum tumor biomarker of disease progression. AFP is usually detected in HCC patients by an antibody based system. Recently, however, aptamers generated from systematic evolution of ligands by exponential enrichment (SELEX) were reported to have an alternative potential in targeted imaging, diagnosis and therapy. In this study, AFP-bound ssDNA aptamers were screened and identified using capillary electrophoresis (CE) SELEX technology. After cloning, sequencing and motif analysis, we successfully confirmed an aptamer, named AP273, specifically targeting AFP. The aptamer could be used as a probe in AFP immunofluorescence imaging in HepG2, one AFP positive cancer cell line, but not in A549, an AFP negative cancer cell line. More interesting, the aptamer efficiently inhibited the migration and invasion of HCC cells after in vivo transfection. Motif analysis revealed that AP273 had several stable secondary motifs in its structure. Our results indicate that CE-SELEX technology is an efficient method to screen specific protein-bound ssDNA, and AP273 could be used as an agent in AFP-based staining, diagnosis and therapy, although more works are still needed. |
format | Online Article Text |
id | pubmed-4620443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46204432015-10-29 Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX Dong, Lili Tan, Qiwen Ye, Wei Liu, Dongli Chen, Haifeng Hu, Hongwei Wen, Duo Liu, Yang Cao, Ya Kang, Jingwu Fan, Jia Guo, Wei Wu, Weizhong Sci Rep Article Alpha-fetoprotein (AFP) is a liver cancer associated protein and has long been utilized as a serum tumor biomarker of disease progression. AFP is usually detected in HCC patients by an antibody based system. Recently, however, aptamers generated from systematic evolution of ligands by exponential enrichment (SELEX) were reported to have an alternative potential in targeted imaging, diagnosis and therapy. In this study, AFP-bound ssDNA aptamers were screened and identified using capillary electrophoresis (CE) SELEX technology. After cloning, sequencing and motif analysis, we successfully confirmed an aptamer, named AP273, specifically targeting AFP. The aptamer could be used as a probe in AFP immunofluorescence imaging in HepG2, one AFP positive cancer cell line, but not in A549, an AFP negative cancer cell line. More interesting, the aptamer efficiently inhibited the migration and invasion of HCC cells after in vivo transfection. Motif analysis revealed that AP273 had several stable secondary motifs in its structure. Our results indicate that CE-SELEX technology is an efficient method to screen specific protein-bound ssDNA, and AP273 could be used as an agent in AFP-based staining, diagnosis and therapy, although more works are still needed. Nature Publishing Group 2015-10-26 /pmc/articles/PMC4620443/ /pubmed/26497223 http://dx.doi.org/10.1038/srep15552 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Dong, Lili Tan, Qiwen Ye, Wei Liu, Dongli Chen, Haifeng Hu, Hongwei Wen, Duo Liu, Yang Cao, Ya Kang, Jingwu Fan, Jia Guo, Wei Wu, Weizhong Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title | Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title_full | Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title_fullStr | Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title_full_unstemmed | Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title_short | Screening and Identifying a Novel ssDNA Aptamer against Alpha-fetoprotein Using CE-SELEX |
title_sort | screening and identifying a novel ssdna aptamer against alpha-fetoprotein using ce-selex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620443/ https://www.ncbi.nlm.nih.gov/pubmed/26497223 http://dx.doi.org/10.1038/srep15552 |
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