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The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation
An anticancer bioactive peptide (ACBP), goat peroxiredoxin-5 (gPRDX5), was identified from goat-spleen extract after immunizing the goat with gastric cancer-cell lysate. Its amino acid sequence was determined by employing 2D nano-LC-ESI-LTQ-Orbitrap MS/MS combined with Mascot database search in the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830999/ https://www.ncbi.nlm.nih.gov/pubmed/27074889 http://dx.doi.org/10.1038/srep24467 |
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author | Feng, Xiaozhou Liu, Juanjuan Fan, Shuai Liu, Fan Li, Yadong Jin, Yuanyuan Bai, Liping Yang, Zhaoyong |
author_facet | Feng, Xiaozhou Liu, Juanjuan Fan, Shuai Liu, Fan Li, Yadong Jin, Yuanyuan Bai, Liping Yang, Zhaoyong |
author_sort | Feng, Xiaozhou |
collection | PubMed |
description | An anticancer bioactive peptide (ACBP), goat peroxiredoxin-5 (gPRDX5), was identified from goat-spleen extract after immunizing the goat with gastric cancer-cell lysate. Its amino acid sequence was determined by employing 2D nano-LC-ESI-LTQ-Orbitrap MS/MS combined with Mascot database search in the goat subset of the Uniprot database. The recombinant gPRDX5 protein was acquired by heterogeneous expression in Escherichia coli. Subsequently, the anti-cancer bioactivity of the peptide was measured by several kinds of tumor cells. The results indicated that the gPRDX5 was a good anti-cancer candidate, especially for killing B16 cells. However, the peptide was found to be unstable without modification with pharmaceutical excipients, which would be a hurdle for future medicinal application. In order to overcome this problem and find an effective way to evaluate the gPRDX5, nanoparticle formation, which has been widely used in drug delivery because of its steadiness in application, less side-effects and enhancement of drug accumulation in target issues, was used here to address the issues. In this work, the gPRDX5 was dispersed into nanoparticles before delivered to B16 cells. By the nanotechnological method, the gPRDX5 was stabilized by a fast and accurate procedure, which suggests a promising way for screening the peptide for further possible medicinal applications. |
format | Online Article Text |
id | pubmed-4830999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48309992016-04-19 The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation Feng, Xiaozhou Liu, Juanjuan Fan, Shuai Liu, Fan Li, Yadong Jin, Yuanyuan Bai, Liping Yang, Zhaoyong Sci Rep Article An anticancer bioactive peptide (ACBP), goat peroxiredoxin-5 (gPRDX5), was identified from goat-spleen extract after immunizing the goat with gastric cancer-cell lysate. Its amino acid sequence was determined by employing 2D nano-LC-ESI-LTQ-Orbitrap MS/MS combined with Mascot database search in the goat subset of the Uniprot database. The recombinant gPRDX5 protein was acquired by heterogeneous expression in Escherichia coli. Subsequently, the anti-cancer bioactivity of the peptide was measured by several kinds of tumor cells. The results indicated that the gPRDX5 was a good anti-cancer candidate, especially for killing B16 cells. However, the peptide was found to be unstable without modification with pharmaceutical excipients, which would be a hurdle for future medicinal application. In order to overcome this problem and find an effective way to evaluate the gPRDX5, nanoparticle formation, which has been widely used in drug delivery because of its steadiness in application, less side-effects and enhancement of drug accumulation in target issues, was used here to address the issues. In this work, the gPRDX5 was dispersed into nanoparticles before delivered to B16 cells. By the nanotechnological method, the gPRDX5 was stabilized by a fast and accurate procedure, which suggests a promising way for screening the peptide for further possible medicinal applications. Nature Publishing Group 2016-04-14 /pmc/articles/PMC4830999/ /pubmed/27074889 http://dx.doi.org/10.1038/srep24467 Text en Copyright © 2016, 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 Feng, Xiaozhou Liu, Juanjuan Fan, Shuai Liu, Fan Li, Yadong Jin, Yuanyuan Bai, Liping Yang, Zhaoyong The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title | The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title_full | The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title_fullStr | The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title_full_unstemmed | The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title_short | The identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
title_sort | identification of goat peroxiredoxin-5 and the evaluation and enhancement of its stability by nanoparticle formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830999/ https://www.ncbi.nlm.nih.gov/pubmed/27074889 http://dx.doi.org/10.1038/srep24467 |
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