Journal article
Isolation of NELL 1 aptamers for rhabdomyosarcoma targeting
- Abstract:
- NELL1 (Neural epidermal growth factor-like (EGFL)-like protein) is an important biomarker associated with tissue and bone development and regeneration. NELL1 upregulation has been linked with metastasis and negative prognosis in rhabdomyosarcoma (RMS). Furthermore, multiple recent studies have also shown the importance of NELL1 in inflammatory bowel disease and membranous nephropathy, amongst other diseases. In this study, several anti-NELL1 DNA aptamers were selected from a randomized ssDNA pool using a fluorescence-guided method and evaluated for their binding affinity and selectivity. Several other methods such as a metabolic assay and confocal microscopy were also applied for the evaluation of the selected aptamers. The top three candidates were evaluated further, and AptNCan3 was shown to have a binding affinity up to 959.2 nM. Selectivity was examined in the RH30 RMS cells that overexpressed NELL1. Both AptNCan2 and AptNCan3 could significantly suppress metabolic activity in RMS cells. AptNCan3 was found to locate on the cell membrane and also on intracellular vesicles, which matched the location of NELL1 shown by antibodies in previous research. These results indicate that the selected anti-NELL1 aptamer showed strong and highly specific binding to NELL1 and therefore has potential to be used for in vitro or in vivo studies and treatments.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, 2.9MB, Terms of use)
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- Publisher copy:
- 10.3390/bioengineering9040174
Authors
- Publisher:
- MDPI
- Journal:
- Bioengineering More from this journal
- Volume:
- 9
- Issue:
- 4
- Article number:
- 174
- Publication date:
- 2022-04-15
- Acceptance date:
- 2022-04-13
- DOI:
- EISSN:
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2306-5354
- Pmid:
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35447734
- Language:
-
English
- Keywords:
- Pubs id:
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1257102
- Local pid:
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pubs:1257102
- Deposit date:
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2022-06-09
Terms of use
- Copyright holder:
- Duan and Townley
- Copyright date:
- 2022
- Rights statement:
- Copyright © 2022 by the authors. 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/).
- Licence:
- CC Attribution (CC BY)
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