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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...

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Autores principales: Kimura, Mitsuhiro, Endo, Akira, Nagira, Yozo, Yoshizumi, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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.
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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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