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Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors

Flagella and cilia are cellular appendages that inherit essential functions of microbial life including sensing and navigating the environment. In order to propel a swimming microorganism they displace the surrounding fluid by means of periodic motions, while precisely timed modulations of their bea...

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Autores principales: Böddeker, Thomas J., Karpitschka, Stefan, Kreis, Christian T., Magdelaine, Quentin, Bäumchen, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014799/
https://www.ncbi.nlm.nih.gov/pubmed/31937233
http://dx.doi.org/10.1098/rsif.2019.0580
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author Böddeker, Thomas J.
Karpitschka, Stefan
Kreis, Christian T.
Magdelaine, Quentin
Bäumchen, Oliver
author_facet Böddeker, Thomas J.
Karpitschka, Stefan
Kreis, Christian T.
Magdelaine, Quentin
Bäumchen, Oliver
author_sort Böddeker, Thomas J.
collection PubMed
description Flagella and cilia are cellular appendages that inherit essential functions of microbial life including sensing and navigating the environment. In order to propel a swimming microorganism they displace the surrounding fluid by means of periodic motions, while precisely timed modulations of their beating patterns enable the cell to steer towards or away from specific locations. Characterizing the dynamic forces, however, is challenging and typically relies on indirect experimental approaches. Here, we present direct in vivo measurements of the dynamic forces of motile Chlamydomonas reinhardtii cells in controlled environments. The experiments are based on partially aspirating a living microorganism at the tip of a micropipette force sensor and optically recording the micropipette’s position fluctuations with high temporal and sub-pixel spatial resolution. Spectral signal analysis allows for isolating the cell-generated dynamic forces caused by the periodic motion of the flagella from background noise. We provide an analytic, elasto-hydrodynamic model for the micropipette force sensor and describe how to obtain the micropipette’s full frequency response function from a dynamic force calibration. Using this approach, we measure the amplitude of the oscillatory forces during the swimming activity of individual Chlamydomonas reinhardtii cells of 26 ± 5 pN, resulting from the coordinated flagellar beating with a frequency of 49 ± 5 Hz. This dynamic micropipette force sensor technique generalizes the applicability of micropipettes as force sensors from static to dynamic force measurements, yielding a force sensitivity in the piconewton range. In addition to measurements in bulk liquid environment, we study the dynamic forces of the biflagellated microswimmer in the vicinity of a solid/liquid interface. As we gradually decrease the distance of the swimming microbe to the interface, we measure a significantly enhanced force transduction at distances larger than the maximum extent of the beating flagella, highlighting the importance of hydrodynamic interactions for scenarios in which flagellated microorganisms encounter surfaces.
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spelling pubmed-70147992020-02-15 Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors Böddeker, Thomas J. Karpitschka, Stefan Kreis, Christian T. Magdelaine, Quentin Bäumchen, Oliver J R Soc Interface Life Sciences–Physics interface Flagella and cilia are cellular appendages that inherit essential functions of microbial life including sensing and navigating the environment. In order to propel a swimming microorganism they displace the surrounding fluid by means of periodic motions, while precisely timed modulations of their beating patterns enable the cell to steer towards or away from specific locations. Characterizing the dynamic forces, however, is challenging and typically relies on indirect experimental approaches. Here, we present direct in vivo measurements of the dynamic forces of motile Chlamydomonas reinhardtii cells in controlled environments. The experiments are based on partially aspirating a living microorganism at the tip of a micropipette force sensor and optically recording the micropipette’s position fluctuations with high temporal and sub-pixel spatial resolution. Spectral signal analysis allows for isolating the cell-generated dynamic forces caused by the periodic motion of the flagella from background noise. We provide an analytic, elasto-hydrodynamic model for the micropipette force sensor and describe how to obtain the micropipette’s full frequency response function from a dynamic force calibration. Using this approach, we measure the amplitude of the oscillatory forces during the swimming activity of individual Chlamydomonas reinhardtii cells of 26 ± 5 pN, resulting from the coordinated flagellar beating with a frequency of 49 ± 5 Hz. This dynamic micropipette force sensor technique generalizes the applicability of micropipettes as force sensors from static to dynamic force measurements, yielding a force sensitivity in the piconewton range. In addition to measurements in bulk liquid environment, we study the dynamic forces of the biflagellated microswimmer in the vicinity of a solid/liquid interface. As we gradually decrease the distance of the swimming microbe to the interface, we measure a significantly enhanced force transduction at distances larger than the maximum extent of the beating flagella, highlighting the importance of hydrodynamic interactions for scenarios in which flagellated microorganisms encounter surfaces. The Royal Society 2020-01 2020-01-15 /pmc/articles/PMC7014799/ /pubmed/31937233 http://dx.doi.org/10.1098/rsif.2019.0580 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Physics interface
Böddeker, Thomas J.
Karpitschka, Stefan
Kreis, Christian T.
Magdelaine, Quentin
Bäumchen, Oliver
Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title_full Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title_fullStr Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title_full_unstemmed Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title_short Dynamic force measurements on swimming Chlamydomonas cells using micropipette force sensors
title_sort dynamic force measurements on swimming chlamydomonas cells using micropipette force sensors
topic Life Sciences–Physics interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014799/
https://www.ncbi.nlm.nih.gov/pubmed/31937233
http://dx.doi.org/10.1098/rsif.2019.0580
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