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Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells
Mesoscale molecular assemblies on the cell surface, such as cilia and filopodia, integrate information, control transport and amplify signals. Designer cell-surface assemblies could control these cellular functions. Such assemblies could be constructed from synthetic components ex vivo, making it po...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484582/ https://www.ncbi.nlm.nih.gov/pubmed/34593818 http://dx.doi.org/10.1038/s41467-021-25890-z |
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author | Jia, Sisi Phua, Siew Cheng Nihongaki, Yuta Li, Yizeng Pacella, Michael Li, Yi Mohammed, Abdul M. Sun, Sean Inoue, Takanari Schulman, Rebecca |
author_facet | Jia, Sisi Phua, Siew Cheng Nihongaki, Yuta Li, Yizeng Pacella, Michael Li, Yi Mohammed, Abdul M. Sun, Sean Inoue, Takanari Schulman, Rebecca |
author_sort | Jia, Sisi |
collection | PubMed |
description | Mesoscale molecular assemblies on the cell surface, such as cilia and filopodia, integrate information, control transport and amplify signals. Designer cell-surface assemblies could control these cellular functions. Such assemblies could be constructed from synthetic components ex vivo, making it possible to form such structures using modern nanoscale self-assembly and fabrication techniques, and then oriented on the cell surface. Here we integrate synthetic devices, micron-scale DNA nanotubes, with mammalian cells by anchoring them by their ends to specific cell surface receptors. These filaments can measure shear stresses between 0-2 dyn/cm(2), a regime important for cell signaling. Nanotubes can also grow while anchored to cells, thus acting as dynamic cell components. This approach to cell surface engineering, in which synthetic biomolecular assemblies are organized with existing cellular architecture, could make it possible to build new types of sensors, machines and scaffolds that can interface with, control and measure properties of cells. |
format | Online Article Text |
id | pubmed-8484582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84845822021-10-22 Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells Jia, Sisi Phua, Siew Cheng Nihongaki, Yuta Li, Yizeng Pacella, Michael Li, Yi Mohammed, Abdul M. Sun, Sean Inoue, Takanari Schulman, Rebecca Nat Commun Article Mesoscale molecular assemblies on the cell surface, such as cilia and filopodia, integrate information, control transport and amplify signals. Designer cell-surface assemblies could control these cellular functions. Such assemblies could be constructed from synthetic components ex vivo, making it possible to form such structures using modern nanoscale self-assembly and fabrication techniques, and then oriented on the cell surface. Here we integrate synthetic devices, micron-scale DNA nanotubes, with mammalian cells by anchoring them by their ends to specific cell surface receptors. These filaments can measure shear stresses between 0-2 dyn/cm(2), a regime important for cell signaling. Nanotubes can also grow while anchored to cells, thus acting as dynamic cell components. This approach to cell surface engineering, in which synthetic biomolecular assemblies are organized with existing cellular architecture, could make it possible to build new types of sensors, machines and scaffolds that can interface with, control and measure properties of cells. Nature Publishing Group UK 2021-09-30 /pmc/articles/PMC8484582/ /pubmed/34593818 http://dx.doi.org/10.1038/s41467-021-25890-z Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jia, Sisi Phua, Siew Cheng Nihongaki, Yuta Li, Yizeng Pacella, Michael Li, Yi Mohammed, Abdul M. Sun, Sean Inoue, Takanari Schulman, Rebecca Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title | Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title_full | Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title_fullStr | Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title_full_unstemmed | Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title_short | Growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
title_sort | growth and site-specific organization of micron-scale biomolecular devices on living mammalian cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484582/ https://www.ncbi.nlm.nih.gov/pubmed/34593818 http://dx.doi.org/10.1038/s41467-021-25890-z |
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