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Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound

Efficient intracellular delivery of biologically active macromolecules has been a challenging but important process for manipulating live cells for research and therapeutic purposes. There have been limited transfection techniques that can deliver multiple types of active molecules simultaneously in...

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Autores principales: Yoon, Sangpil, Wang, Pengzhi, Peng, Qin, Wang, Yingxiao, Shung, K. Kirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509725/
https://www.ncbi.nlm.nih.gov/pubmed/28706248
http://dx.doi.org/10.1038/s41598-017-05722-1
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author Yoon, Sangpil
Wang, Pengzhi
Peng, Qin
Wang, Yingxiao
Shung, K. Kirk
author_facet Yoon, Sangpil
Wang, Pengzhi
Peng, Qin
Wang, Yingxiao
Shung, K. Kirk
author_sort Yoon, Sangpil
collection PubMed
description Efficient intracellular delivery of biologically active macromolecules has been a challenging but important process for manipulating live cells for research and therapeutic purposes. There have been limited transfection techniques that can deliver multiple types of active molecules simultaneously into single-cells as well as different types of molecules into physically connected individual neighboring cells separately with high precision and low cytotoxicity. Here, a high frequency ultrasound-based remote intracellular delivery technique capable of delivery of multiple DNA plasmids, messenger RNAs, and recombinant proteins is developed to allow high spatiotemporal visualization and analysis of gene and protein expressions as well as single-cell gene editing using clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein-9 nuclease (Cas9), a method called acoustic-transfection. Acoustic-transfection has advantages over typical sonoporation because acoustic-transfection utilizing ultra-high frequency ultrasound over 150 MHz can directly deliver gene and proteins into cytoplasm without microbubbles, which enables controlled and local intracellular delivery to acoustic-transfection technique. Acoustic-transfection was further demonstrated to deliver CRISPR-Cas9 systems to successfully modify and reprogram the genome of single live cells, providing the evidence of the acoustic-transfection technique for precise genome editing using CRISPR-Cas9.
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spelling pubmed-55097252017-07-17 Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound Yoon, Sangpil Wang, Pengzhi Peng, Qin Wang, Yingxiao Shung, K. Kirk Sci Rep Article Efficient intracellular delivery of biologically active macromolecules has been a challenging but important process for manipulating live cells for research and therapeutic purposes. There have been limited transfection techniques that can deliver multiple types of active molecules simultaneously into single-cells as well as different types of molecules into physically connected individual neighboring cells separately with high precision and low cytotoxicity. Here, a high frequency ultrasound-based remote intracellular delivery technique capable of delivery of multiple DNA plasmids, messenger RNAs, and recombinant proteins is developed to allow high spatiotemporal visualization and analysis of gene and protein expressions as well as single-cell gene editing using clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein-9 nuclease (Cas9), a method called acoustic-transfection. Acoustic-transfection has advantages over typical sonoporation because acoustic-transfection utilizing ultra-high frequency ultrasound over 150 MHz can directly deliver gene and proteins into cytoplasm without microbubbles, which enables controlled and local intracellular delivery to acoustic-transfection technique. Acoustic-transfection was further demonstrated to deliver CRISPR-Cas9 systems to successfully modify and reprogram the genome of single live cells, providing the evidence of the acoustic-transfection technique for precise genome editing using CRISPR-Cas9. Nature Publishing Group UK 2017-07-13 /pmc/articles/PMC5509725/ /pubmed/28706248 http://dx.doi.org/10.1038/s41598-017-05722-1 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoon, Sangpil
Wang, Pengzhi
Peng, Qin
Wang, Yingxiao
Shung, K. Kirk
Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title_full Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title_fullStr Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title_full_unstemmed Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title_short Acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
title_sort acoustic-transfection for genomic manipulation of single-cells using high frequency ultrasound
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509725/
https://www.ncbi.nlm.nih.gov/pubmed/28706248
http://dx.doi.org/10.1038/s41598-017-05722-1
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