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Micropipette-based biomechanical nanotools on living cells
Mechanobiology is an emerging field at the interface of biology and mechanics, investigating the roles of mechanical forces within biomolecules, organelles, cells, and tissues. As a highlight, the recent advances of micropipette-based aspiration assays and dynamic force spectroscopies such as biomem...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964576/ https://www.ncbi.nlm.nih.gov/pubmed/35171346 http://dx.doi.org/10.1007/s00249-021-01587-5 |
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author | Wang, Haoqing Zhou, Fang Guo, Yuze Ju, Lining Arnold |
author_facet | Wang, Haoqing Zhou, Fang Guo, Yuze Ju, Lining Arnold |
author_sort | Wang, Haoqing |
collection | PubMed |
description | Mechanobiology is an emerging field at the interface of biology and mechanics, investigating the roles of mechanical forces within biomolecules, organelles, cells, and tissues. As a highlight, the recent advances of micropipette-based aspiration assays and dynamic force spectroscopies such as biomembrane force probe (BFP) provide unprecedented mechanobiological insights with excellent live-cell compatibility. In their classic applications, these assays measure force-dependent ligand–receptor-binding kinetics, protein conformational changes, and cellular mechanical properties such as cortical tension and stiffness. In recent years, when combined with advanced microscopies in high spatial and temporal resolutions, these biomechanical nanotools enable characterization of receptor-mediated cell mechanosensing and subsequent organelle behaviors at single-cellular and molecular level. In this review, we summarize the latest developments of these assays for live-cell mechanobiology studies. We also provide perspectives on their future upgrades with multimodal integration and high-throughput capability. |
format | Online Article Text |
id | pubmed-8964576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-89645762022-04-07 Micropipette-based biomechanical nanotools on living cells Wang, Haoqing Zhou, Fang Guo, Yuze Ju, Lining Arnold Eur Biophys J Review Mechanobiology is an emerging field at the interface of biology and mechanics, investigating the roles of mechanical forces within biomolecules, organelles, cells, and tissues. As a highlight, the recent advances of micropipette-based aspiration assays and dynamic force spectroscopies such as biomembrane force probe (BFP) provide unprecedented mechanobiological insights with excellent live-cell compatibility. In their classic applications, these assays measure force-dependent ligand–receptor-binding kinetics, protein conformational changes, and cellular mechanical properties such as cortical tension and stiffness. In recent years, when combined with advanced microscopies in high spatial and temporal resolutions, these biomechanical nanotools enable characterization of receptor-mediated cell mechanosensing and subsequent organelle behaviors at single-cellular and molecular level. In this review, we summarize the latest developments of these assays for live-cell mechanobiology studies. We also provide perspectives on their future upgrades with multimodal integration and high-throughput capability. Springer International Publishing 2022-02-16 2022 /pmc/articles/PMC8964576/ /pubmed/35171346 http://dx.doi.org/10.1007/s00249-021-01587-5 Text en © The Author(s) 2022 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/) . |
spellingShingle | Review Wang, Haoqing Zhou, Fang Guo, Yuze Ju, Lining Arnold Micropipette-based biomechanical nanotools on living cells |
title | Micropipette-based biomechanical nanotools on living cells |
title_full | Micropipette-based biomechanical nanotools on living cells |
title_fullStr | Micropipette-based biomechanical nanotools on living cells |
title_full_unstemmed | Micropipette-based biomechanical nanotools on living cells |
title_short | Micropipette-based biomechanical nanotools on living cells |
title_sort | micropipette-based biomechanical nanotools on living cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964576/ https://www.ncbi.nlm.nih.gov/pubmed/35171346 http://dx.doi.org/10.1007/s00249-021-01587-5 |
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