Abstract
The measurement of cell membrane potential (V m) is important for understanding ion channel function. V m plays a role in several routine cellular functions and diseases, particularly in excitable cells such as muscle and nerve. However, measuring V m is difficult, relying either on labour-intensive direct measurement of single cells (intracellular electrodes, patch clamp) or indirect measurement of fluorescence intensity, using V m-sensitive labels. Here we demonstrate a direct measurement technique based on determination of the cell’s ζ-potential, the electrical potential at the hydrodynamic shear plane, approximately 1 nm beyond the cell surface. We demonstrate this principle using excitable H9c2 cardiomyoblasts, measured in both polarised and depolarised states, before and after extracellular intervention to alter cell ion concentration. Given widespread availability of ζ-potential measurement apparatus (most typically in chemistry and materials science settings), this offers a new method of measuring V m without the need for fluorescence measurements or calibration curves.
Original language | British English |
---|---|
Article number | 055701 |
Journal | Measurement Science and Technology |
Volume | 35 |
Issue number | 5 |
DOIs | |
State | Published - May 2024 |
Keywords
- action potential
- excitable cell
- H9c2 cardiomyoblasts
- RMP
- zeta potential
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Chacar, S., Catacutan, M. K., Albakr, S., Al Safar, H., Babiker, S., Ahmed, S., Albizreh, A. A., Alshehhi, A. Z., Lee, S., Nader, M. (2024). Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential. Measurement Science and Technology, 35(5), Article 055701. https://doi.org/10.1088/1361-6501/ad25de
Chacar, Stephanie ; Catacutan, Mary Krystelle ; Albakr, Shamma et al. / Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential. In: Measurement Science and Technology. 2024 ; Vol. 35, No. 5.
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title = "Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential",
abstract = "The measurement of cell membrane potential (V m) is important for understanding ion channel function. V m plays a role in several routine cellular functions and diseases, particularly in excitable cells such as muscle and nerve. However, measuring V m is difficult, relying either on labour-intensive direct measurement of single cells (intracellular electrodes, patch clamp) or indirect measurement of fluorescence intensity, using V m-sensitive labels. Here we demonstrate a direct measurement technique based on determination of the cell{\textquoteright}s ζ-potential, the electrical potential at the hydrodynamic shear plane, approximately 1 nm beyond the cell surface. We demonstrate this principle using excitable H9c2 cardiomyoblasts, measured in both polarised and depolarised states, before and after extracellular intervention to alter cell ion concentration. Given widespread availability of ζ-potential measurement apparatus (most typically in chemistry and materials science settings), this offers a new method of measuring V m without the need for fluorescence measurements or calibration curves.",
keywords = "action potential, excitable cell, H9c2 cardiomyoblasts, RMP, zeta potential",
author = "Stephanie Chacar and Catacutan, {Mary Krystelle} and Shamma Albakr and {Al Safar}, Habiba and Samira Babiker and Samar Ahmed and Albizreh, {Anas A.} and Alshehhi, {Ahmed Z.} and Sungmun Lee and Moni Nader and Hughes, {Michael Pycraft}",
note = "Publisher Copyright: {\textcopyright} 2024 The Author(s). Published by IOP Publishing Ltd.",
year = "2024",
month = may,
doi = "10.1088/1361-6501/ad25de",
language = "British English",
volume = "35",
journal = "Measurement Science and Technology",
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Chacar, S, Catacutan, MK, Albakr, S, Al Safar, H, Babiker, S, Ahmed, S, Albizreh, AA, Alshehhi, AZ, Lee, S, Nader, M 2024, 'Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential', Measurement Science and Technology, vol. 35, no. 5, 055701. https://doi.org/10.1088/1361-6501/ad25de
Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential. / Chacar, Stephanie; Catacutan, Mary Krystelle; Albakr, Shamma et al.
In: Measurement Science and Technology, Vol. 35, No. 5, 055701, 05.2024.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential
AU - Chacar, Stephanie
AU - Catacutan, Mary Krystelle
AU - Albakr, Shamma
AU - Al Safar, Habiba
AU - Babiker, Samira
AU - Ahmed, Samar
AU - Albizreh, Anas A.
AU - Alshehhi, Ahmed Z.
AU - Lee, Sungmun
AU - Nader, Moni
AU - Hughes, Michael Pycraft
N1 - Publisher Copyright:© 2024 The Author(s). Published by IOP Publishing Ltd.
PY - 2024/5
Y1 - 2024/5
N2 - The measurement of cell membrane potential (V m) is important for understanding ion channel function. V m plays a role in several routine cellular functions and diseases, particularly in excitable cells such as muscle and nerve. However, measuring V m is difficult, relying either on labour-intensive direct measurement of single cells (intracellular electrodes, patch clamp) or indirect measurement of fluorescence intensity, using V m-sensitive labels. Here we demonstrate a direct measurement technique based on determination of the cell’s ζ-potential, the electrical potential at the hydrodynamic shear plane, approximately 1 nm beyond the cell surface. We demonstrate this principle using excitable H9c2 cardiomyoblasts, measured in both polarised and depolarised states, before and after extracellular intervention to alter cell ion concentration. Given widespread availability of ζ-potential measurement apparatus (most typically in chemistry and materials science settings), this offers a new method of measuring V m without the need for fluorescence measurements or calibration curves.
AB - The measurement of cell membrane potential (V m) is important for understanding ion channel function. V m plays a role in several routine cellular functions and diseases, particularly in excitable cells such as muscle and nerve. However, measuring V m is difficult, relying either on labour-intensive direct measurement of single cells (intracellular electrodes, patch clamp) or indirect measurement of fluorescence intensity, using V m-sensitive labels. Here we demonstrate a direct measurement technique based on determination of the cell’s ζ-potential, the electrical potential at the hydrodynamic shear plane, approximately 1 nm beyond the cell surface. We demonstrate this principle using excitable H9c2 cardiomyoblasts, measured in both polarised and depolarised states, before and after extracellular intervention to alter cell ion concentration. Given widespread availability of ζ-potential measurement apparatus (most typically in chemistry and materials science settings), this offers a new method of measuring V m without the need for fluorescence measurements or calibration curves.
KW - action potential
KW - excitable cell
KW - H9c2 cardiomyoblasts
KW - RMP
KW - zeta potential
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DO - 10.1088/1361-6501/ad25de
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SN - 0957-0233
VL - 35
JO - Measurement Science and Technology
JF - Measurement Science and Technology
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ER -
Chacar S, Catacutan MK, Albakr S, Al Safar H, Babiker S, Ahmed S et al. Rapid, label-free, contactless measurement of membrane potential in excitable H9c2 cardiomyoblasts using ζ-potential. Measurement Science and Technology. 2024 May;35(5):055701. doi: 10.1088/1361-6501/ad25de