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A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis

Suitable immobilisation of microorganisms and single cells is key for high-resolution topographical imaging and study of mechanical properties with atomic force microscopy (AFM) under physiologically relevant conditions. Sample preparation techniques must be able to withstand the forces exerted by t...

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Detalles Bibliográficos
Autores principales: Evans, Christopher T., Baldock, Sara J., Hardy, John G., Payton, Oliver, Picco, Loren, Allen, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066395/
https://www.ncbi.nlm.nih.gov/pubmed/33806176
http://dx.doi.org/10.3390/microorganisms9040680
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author Evans, Christopher T.
Baldock, Sara J.
Hardy, John G.
Payton, Oliver
Picco, Loren
Allen, Michael J.
author_facet Evans, Christopher T.
Baldock, Sara J.
Hardy, John G.
Payton, Oliver
Picco, Loren
Allen, Michael J.
author_sort Evans, Christopher T.
collection PubMed
description Suitable immobilisation of microorganisms and single cells is key for high-resolution topographical imaging and study of mechanical properties with atomic force microscopy (AFM) under physiologically relevant conditions. Sample preparation techniques must be able to withstand the forces exerted by the Z range-limited cantilever tip, and not negatively affect the sample surface for data acquisition. Here, we describe an inherently flexible methodology, utilising the high-resolution three-dimensional based printing technique of multiphoton polymerisation to rapidly generate bespoke arrays for cellular AFM analysis. As an example, we present data collected from live Emiliania huxleyi cells, unicellular microalgae, imaged by contact mode High-Speed Atomic Force Microscopy (HS-AFM), including one cell that was imaged continuously for over 90 min.
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spelling pubmed-80663952021-04-25 A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis Evans, Christopher T. Baldock, Sara J. Hardy, John G. Payton, Oliver Picco, Loren Allen, Michael J. Microorganisms Article Suitable immobilisation of microorganisms and single cells is key for high-resolution topographical imaging and study of mechanical properties with atomic force microscopy (AFM) under physiologically relevant conditions. Sample preparation techniques must be able to withstand the forces exerted by the Z range-limited cantilever tip, and not negatively affect the sample surface for data acquisition. Here, we describe an inherently flexible methodology, utilising the high-resolution three-dimensional based printing technique of multiphoton polymerisation to rapidly generate bespoke arrays for cellular AFM analysis. As an example, we present data collected from live Emiliania huxleyi cells, unicellular microalgae, imaged by contact mode High-Speed Atomic Force Microscopy (HS-AFM), including one cell that was imaged continuously for over 90 min. MDPI 2021-03-25 /pmc/articles/PMC8066395/ /pubmed/33806176 http://dx.doi.org/10.3390/microorganisms9040680 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Evans, Christopher T.
Baldock, Sara J.
Hardy, John G.
Payton, Oliver
Picco, Loren
Allen, Michael J.
A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title_full A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title_fullStr A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title_full_unstemmed A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title_short A Non-Destructive, Tuneable Method to Isolate Live Cells for High-Speed AFM Analysis
title_sort non-destructive, tuneable method to isolate live cells for high-speed afm analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066395/
https://www.ncbi.nlm.nih.gov/pubmed/33806176
http://dx.doi.org/10.3390/microorganisms9040680
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