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Universal intracellular biomolecule delivery with precise dosage control
Intracellular delivery of mRNA, DNA, and other large macromolecules into cells plays an essential role in an array of biological research and clinical therapies. However, current methods yield a wide variation in the amount of material delivered, as well as limitations on the cell types and cargoes...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209385/ https://www.ncbi.nlm.nih.gov/pubmed/30402539 http://dx.doi.org/10.1126/sciadv.aat8131 |
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author | Cao, Y. Chen, H. Qiu, R. Hanna, M. Ma, E. Hjort, M. Zhang, A. Lewis, R. S. Wu, J. C. Melosh, N. A. |
author_facet | Cao, Y. Chen, H. Qiu, R. Hanna, M. Ma, E. Hjort, M. Zhang, A. Lewis, R. S. Wu, J. C. Melosh, N. A. |
author_sort | Cao, Y. |
collection | PubMed |
description | Intracellular delivery of mRNA, DNA, and other large macromolecules into cells plays an essential role in an array of biological research and clinical therapies. However, current methods yield a wide variation in the amount of material delivered, as well as limitations on the cell types and cargoes possible. Here, we demonstrate quantitatively controlled delivery into a range of primary cells and cell lines with a tight dosage distribution using a nanostraw-electroporation system (NES). In NES, cells are cultured onto track-etched membranes with protruding nanostraws that connect to the fluidic environment beneath the membrane. The tight cell-nanostraw interface focuses applied electric fields to the cell membrane, enabling low-voltage and nondamaging local poration of the cell membrane. Concurrently, the field electrophoretically injects biomolecular cargoes through the nanostraws and into the cell at the same location. We show that the amount of material delivered is precisely controlled by the applied voltage, delivery duration, and reagent concentration. NES is highly effective even for primary cell types or different cell densities, is largely cargo agnostic, and can simultaneously deliver specific ratios of different molecules. Using a simple cell culture well format, the NES delivers into >100,000 cells within 20 s with >95% cell viability, enabling facile, dosage-controlled intracellular delivery for a wide variety of biological applications. |
format | Online Article Text |
id | pubmed-6209385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62093852018-11-06 Universal intracellular biomolecule delivery with precise dosage control Cao, Y. Chen, H. Qiu, R. Hanna, M. Ma, E. Hjort, M. Zhang, A. Lewis, R. S. Wu, J. C. Melosh, N. A. Sci Adv Research Articles Intracellular delivery of mRNA, DNA, and other large macromolecules into cells plays an essential role in an array of biological research and clinical therapies. However, current methods yield a wide variation in the amount of material delivered, as well as limitations on the cell types and cargoes possible. Here, we demonstrate quantitatively controlled delivery into a range of primary cells and cell lines with a tight dosage distribution using a nanostraw-electroporation system (NES). In NES, cells are cultured onto track-etched membranes with protruding nanostraws that connect to the fluidic environment beneath the membrane. The tight cell-nanostraw interface focuses applied electric fields to the cell membrane, enabling low-voltage and nondamaging local poration of the cell membrane. Concurrently, the field electrophoretically injects biomolecular cargoes through the nanostraws and into the cell at the same location. We show that the amount of material delivered is precisely controlled by the applied voltage, delivery duration, and reagent concentration. NES is highly effective even for primary cell types or different cell densities, is largely cargo agnostic, and can simultaneously deliver specific ratios of different molecules. Using a simple cell culture well format, the NES delivers into >100,000 cells within 20 s with >95% cell viability, enabling facile, dosage-controlled intracellular delivery for a wide variety of biological applications. American Association for the Advancement of Science 2018-10-31 /pmc/articles/PMC6209385/ /pubmed/30402539 http://dx.doi.org/10.1126/sciadv.aat8131 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Cao, Y. Chen, H. Qiu, R. Hanna, M. Ma, E. Hjort, M. Zhang, A. Lewis, R. S. Wu, J. C. Melosh, N. A. Universal intracellular biomolecule delivery with precise dosage control |
title | Universal intracellular biomolecule delivery with precise dosage control |
title_full | Universal intracellular biomolecule delivery with precise dosage control |
title_fullStr | Universal intracellular biomolecule delivery with precise dosage control |
title_full_unstemmed | Universal intracellular biomolecule delivery with precise dosage control |
title_short | Universal intracellular biomolecule delivery with precise dosage control |
title_sort | universal intracellular biomolecule delivery with precise dosage control |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209385/ https://www.ncbi.nlm.nih.gov/pubmed/30402539 http://dx.doi.org/10.1126/sciadv.aat8131 |
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