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A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX
General cancer-targeted ligands that can deliver drugs to cells have been given considerable attention. In this paper, a high-affinity DNA aptamer (HG1) generally binding to human tumor cells was evolved by cell-SELEX, and was further optimized to have 35 deoxynucleotides (HG1-9). Aptamer HG1-9 coul...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396340/ https://www.ncbi.nlm.nih.gov/pubmed/34445629 http://dx.doi.org/10.3390/ijms22168923 |
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author | Zhang, Nan Bing, Tao Shen, Luyao Feng, Le Liu, Xiangjun Shangguan, Dihua |
author_facet | Zhang, Nan Bing, Tao Shen, Luyao Feng, Le Liu, Xiangjun Shangguan, Dihua |
author_sort | Zhang, Nan |
collection | PubMed |
description | General cancer-targeted ligands that can deliver drugs to cells have been given considerable attention. In this paper, a high-affinity DNA aptamer (HG1) generally binding to human tumor cells was evolved by cell-SELEX, and was further optimized to have 35 deoxynucleotides (HG1-9). Aptamer HG1-9 could be taken up by live cells, and its target protein on a cell was identified to be human transferrin receptor (TfR). As a man-made ligand of TfR, aptamer HG1-9 was demonstrated to bind at the same site of human TfR as transferrin with comparable binding affinity, and was proved to cross the epithelium barrier through transferrin receptor-mediated transcytosis. These results suggest that aptamer HG1-9 holds potential as a promising ligand to develop general cancer-targeted diagnostics and therapeutics. |
format | Online Article Text |
id | pubmed-8396340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83963402021-08-28 A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX Zhang, Nan Bing, Tao Shen, Luyao Feng, Le Liu, Xiangjun Shangguan, Dihua Int J Mol Sci Article General cancer-targeted ligands that can deliver drugs to cells have been given considerable attention. In this paper, a high-affinity DNA aptamer (HG1) generally binding to human tumor cells was evolved by cell-SELEX, and was further optimized to have 35 deoxynucleotides (HG1-9). Aptamer HG1-9 could be taken up by live cells, and its target protein on a cell was identified to be human transferrin receptor (TfR). As a man-made ligand of TfR, aptamer HG1-9 was demonstrated to bind at the same site of human TfR as transferrin with comparable binding affinity, and was proved to cross the epithelium barrier through transferrin receptor-mediated transcytosis. These results suggest that aptamer HG1-9 holds potential as a promising ligand to develop general cancer-targeted diagnostics and therapeutics. MDPI 2021-08-19 /pmc/articles/PMC8396340/ /pubmed/34445629 http://dx.doi.org/10.3390/ijms22168923 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Nan Bing, Tao Shen, Luyao Feng, Le Liu, Xiangjun Shangguan, Dihua A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title | A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title_full | A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title_fullStr | A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title_full_unstemmed | A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title_short | A DNA Aptameric Ligand of Human Transferrin Receptor Generated by Cell-SELEX |
title_sort | dna aptameric ligand of human transferrin receptor generated by cell-selex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396340/ https://www.ncbi.nlm.nih.gov/pubmed/34445629 http://dx.doi.org/10.3390/ijms22168923 |
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