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Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay
OBJECTIVE: A centrifugation-assisted peptide-mediated gene transfer (CAPT) method was recently developed as an efficient system for gene delivery into plant cells. However, the gene transfer efficiency of CAPT into plant cells was not entirely satisfactory for detecting transient expression of a tra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080836/ https://www.ncbi.nlm.nih.gov/pubmed/37024962 http://dx.doi.org/10.1186/s13104-023-06320-3 |
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author | Kimura, Mitsuhiro Endo, Akira Nagira, Yozo Yoshizumi, Takeshi |
author_facet | Kimura, Mitsuhiro Endo, Akira Nagira, Yozo Yoshizumi, Takeshi |
author_sort | Kimura, Mitsuhiro |
collection | PubMed |
description | OBJECTIVE: A centrifugation-assisted peptide-mediated gene transfer (CAPT) method was recently developed as an efficient system for gene delivery into plant cells. However, the gene transfer efficiency of CAPT into plant cells was not entirely satisfactory for detecting transient expression of a transgene driven into mitochondria. Here, we report a new gene delivery system using a method called particle bombardment-assisted peptide-mediated gene transfer (PBPT). RESULTS: We investigated various parameters of the PBPT method to increase transient gene expression efficiency in Brassica campestris. The optimal conditions for PBPT were a single bombardment with gold particles coated with a DNA‒peptide complex (6 µg of DNA and 2 µg of peptide) at an acceleration pressure of 5 kg/cm(2) and a target distance of 12.5 cm. Moreover, bombardment under the optimal conditions successfully transferred the transgene into the cells of other plant species, namely B. juncea and tomato. Thus, we developed a PBPT method for highly efficient delivery of a DNA‒peptide complex into plant mitochondria. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06320-3. |
format | Online Article Text |
id | pubmed-10080836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100808362023-04-08 Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay Kimura, Mitsuhiro Endo, Akira Nagira, Yozo Yoshizumi, Takeshi BMC Res Notes Research Note OBJECTIVE: A centrifugation-assisted peptide-mediated gene transfer (CAPT) method was recently developed as an efficient system for gene delivery into plant cells. However, the gene transfer efficiency of CAPT into plant cells was not entirely satisfactory for detecting transient expression of a transgene driven into mitochondria. Here, we report a new gene delivery system using a method called particle bombardment-assisted peptide-mediated gene transfer (PBPT). RESULTS: We investigated various parameters of the PBPT method to increase transient gene expression efficiency in Brassica campestris. The optimal conditions for PBPT were a single bombardment with gold particles coated with a DNA‒peptide complex (6 µg of DNA and 2 µg of peptide) at an acceleration pressure of 5 kg/cm(2) and a target distance of 12.5 cm. Moreover, bombardment under the optimal conditions successfully transferred the transgene into the cells of other plant species, namely B. juncea and tomato. Thus, we developed a PBPT method for highly efficient delivery of a DNA‒peptide complex into plant mitochondria. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06320-3. BioMed Central 2023-04-06 /pmc/articles/PMC10080836/ /pubmed/37024962 http://dx.doi.org/10.1186/s13104-023-06320-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Kimura, Mitsuhiro Endo, Akira Nagira, Yozo Yoshizumi, Takeshi Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title | Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title_full | Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title_fullStr | Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title_full_unstemmed | Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title_short | Particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
title_sort | particle bombardment-assisted peptide-mediated gene transfer for highly efficient transient assay |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080836/ https://www.ncbi.nlm.nih.gov/pubmed/37024962 http://dx.doi.org/10.1186/s13104-023-06320-3 |
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