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Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy

Gene therapy offers potentially transformative strategies for major human diseases. However, one of the key challenges in gene therapy is developing an effective strategy that could deliver genes into the specific tissue. Here, we report a novel virus-like nanoparticle, the bioorthgonal engineered v...

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Autores principales: Bao, Chun-Jie, Duan, Jia-Lun, Xie, Ying, Feng, Xin-Ping, Cui, Wei, Chen, Song-Yue, Li, Pei-Shan, Liu, Yi-Xuan, Wang, Jin-Ling, Wang, Gui-Ling, Lu, Wan-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423197/
https://www.ncbi.nlm.nih.gov/pubmed/37572220
http://dx.doi.org/10.1007/s40820-023-01153-y
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author Bao, Chun-Jie
Duan, Jia-Lun
Xie, Ying
Feng, Xin-Ping
Cui, Wei
Chen, Song-Yue
Li, Pei-Shan
Liu, Yi-Xuan
Wang, Jin-Ling
Wang, Gui-Ling
Lu, Wan-Liang
author_facet Bao, Chun-Jie
Duan, Jia-Lun
Xie, Ying
Feng, Xin-Ping
Cui, Wei
Chen, Song-Yue
Li, Pei-Shan
Liu, Yi-Xuan
Wang, Jin-Ling
Wang, Gui-Ling
Lu, Wan-Liang
author_sort Bao, Chun-Jie
collection PubMed
description Gene therapy offers potentially transformative strategies for major human diseases. However, one of the key challenges in gene therapy is developing an effective strategy that could deliver genes into the specific tissue. Here, we report a novel virus-like nanoparticle, the bioorthgonal engineered virus-like recombinant biosome (reBiosome), for efficient gene therapies of cancer and inflammatory diseases. The mutant virus-like biosome (mBiosome) is first prepared by site-specific codon mutation for displaying 4-azido-L-phenylalanine on vesicular stomatitis virus glycoprotein of eBiosome at a rational site, and the reBiosome is then prepared by clicking weak acid-responsive hydrophilic polymer onto the mBiosome via bioorthogonal chemistry. The results show that the reBiosome exhibits reduced virus-like immunogenicity, prolonged blood circulation time and enhanced gene delivery efficiency to weakly acidic foci (like tumor and arthritic tissue). Furthermore, reBiosome demonstrates robust therapeutic efficacy in breast cancer and arthritis by delivering gene editing and silencing systems, respectively. In conclusion, this study develops a universal, safe and efficient platform for gene therapies for cancer and inflammatory diseases. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-023-01153-y.
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spelling pubmed-104231972023-08-14 Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy Bao, Chun-Jie Duan, Jia-Lun Xie, Ying Feng, Xin-Ping Cui, Wei Chen, Song-Yue Li, Pei-Shan Liu, Yi-Xuan Wang, Jin-Ling Wang, Gui-Ling Lu, Wan-Liang Nanomicro Lett Article Gene therapy offers potentially transformative strategies for major human diseases. However, one of the key challenges in gene therapy is developing an effective strategy that could deliver genes into the specific tissue. Here, we report a novel virus-like nanoparticle, the bioorthgonal engineered virus-like recombinant biosome (reBiosome), for efficient gene therapies of cancer and inflammatory diseases. The mutant virus-like biosome (mBiosome) is first prepared by site-specific codon mutation for displaying 4-azido-L-phenylalanine on vesicular stomatitis virus glycoprotein of eBiosome at a rational site, and the reBiosome is then prepared by clicking weak acid-responsive hydrophilic polymer onto the mBiosome via bioorthogonal chemistry. The results show that the reBiosome exhibits reduced virus-like immunogenicity, prolonged blood circulation time and enhanced gene delivery efficiency to weakly acidic foci (like tumor and arthritic tissue). Furthermore, reBiosome demonstrates robust therapeutic efficacy in breast cancer and arthritis by delivering gene editing and silencing systems, respectively. In conclusion, this study develops a universal, safe and efficient platform for gene therapies for cancer and inflammatory diseases. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-023-01153-y. Springer Nature Singapore 2023-08-12 /pmc/articles/PMC10423197/ /pubmed/37572220 http://dx.doi.org/10.1007/s40820-023-01153-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Bao, Chun-Jie
Duan, Jia-Lun
Xie, Ying
Feng, Xin-Ping
Cui, Wei
Chen, Song-Yue
Li, Pei-Shan
Liu, Yi-Xuan
Wang, Jin-Ling
Wang, Gui-Ling
Lu, Wan-Liang
Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title_full Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title_fullStr Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title_full_unstemmed Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title_short Bioorthogonal Engineered Virus-Like Nanoparticles for Efficient Gene Therapy
title_sort bioorthogonal engineered virus-like nanoparticles for efficient gene therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423197/
https://www.ncbi.nlm.nih.gov/pubmed/37572220
http://dx.doi.org/10.1007/s40820-023-01153-y
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