Skip to content
DraconiticResearch
Search Sources API
197,787 studies31 sourcesUpdated 52 min ago
PreprintCC BYbioRxiv

Robust High-Throughput Flickering Spectroscopy for Measurements of Red Blood Cell Membrane Mechanics

  1. 1Unversity of Cambridge

Abstract

The mechanical properties of red blood cell (RBC) membranes are critical to their function in oxygen delivery, and changes to these properties as RBCs age affect their journey around the circulatory system, including clearance by the spleen. Such changes can also have significant health effects,including in cardiovascular disease and on the interactions between RBCs and malaria parasites. The function of RBCs requires them to be very soft, which together with the small size of the cells brings the energy required for measurable deformation of the membrane into the range of typical thermal energies. Red Blood Cells can be observed to flicker under optical microscopy, and these shape fluctuations can be quantified and used to obtain key biophysical parameters such as the tension and bending modulus of the membrane. Typically the shape of the cell's equator is extracted, and the mean power spectrum is obtained by time-averaging the power present in the normal modes of the thermal fluctuations. Flickering spectroscopy has been used extensively on RBCs, but has so far been very low throughput and with some technical limitations. Here we address issues related to active versus passive fluctuations, focusing and optics, camera exposure and sampling, and fast contour detection. In combination with an automated imaging system it is possible to measure thousands of cells in one day, with no user input. We validate this new pipeline by chemical modification of RBC mechanics, and by comparison with simulated fluctuations including each confounding effect. The methods and codes for this robust flickering analysis will allow consistent measurements across labs.

Related

  1. Neuronal lipid composition regulates distinct states of full-length tau assembly, mechanics and membrane interactions
    A. K. Mahakud, A. S. Modak, S. Singh +5
    bioRxivPreprintAll rights reservedFull textBiophysicsbioRxiv
  2. High-throughput affinity profiling of antibodies against soluble and native membrane targets by digital flow cytometry
    Y. Cheng, S. Barcy, B. Fujimoto +3
    bioRxivPreprintCC BY-NC-NDFull textBiophysicsbioRxiv
  3. Optical control of membrane mechanics via global and red-light-catalyzed, leaflet-selective photolipid switching
    R. Yadav, J. Pfeffermann, P. Pohl
    bioRxivPreprintCC BY-NDFull textBiophysicsbioRxiv
  4. Ether linkages in phospholipids provide modular control of membrane mechanics
    J. R. Winnikoff, S. J. Vargas-Urbano, D. Milshteyn +8
    bioRxivPreprintCC BY-NCFull text1 citedBiophysicsbioRxiv
  5. Recursive feedback between Piezo1 conformation and membrane mechanics drives self-organization into finite clusters
    Z. Guo, A. Bagchi, M. Dhankhar +2
    bioRxivPreprintCC BYFull textBiophysicsbioRxiv
BibTeX
@misc{ayazi2026robust,
  title = {{Robust High-Throughput Flickering Spectroscopy for Measurements of Red Blood Cell Membrane Mechanics}},
  author = {F. Ayazi and J. Kotar and J. C. Rayner and P. Cicuta},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.16.751779},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.16.751779v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Robust High-Throughput Flickering Spectroscopy for Measurements of Red Blood Cell Membrane Mechanics
AU  - F. Ayazi
AU  - J. Kotar
AU  - J. C. Rayner
AU  - P. Cicuta
PY  - 2026
DA  - 2026/09/16
PB  - bioRxiv
DO  - 10.64898/2026.09.16.751779
UR  - https://www.biorxiv.org/content/10.64898/2026.09.16.751779v1
AB  - The mechanical properties of red blood cell (RBC) membranes are critical to their function in oxygen delivery, and changes to these properties as RBCs age affect their journey around the circulatory system, including clearance by the spleen. Such changes can also have significant health effects,including in cardiovascular disease and on the interactions between RBCs and malaria parasites. The function of RBCs requires them to be very soft, which together with the small size of the cells brings the energy required for measurable deformation of the membrane into the range of typical thermal energies. Red Blood Cells can be observed to flicker under optical microscopy, and these shape fluctuations can be quantified and used to obtain key biophysical parameters such as the tension and bending modulus of the membrane. Typically the shape of the cell's equator is extracted, and the mean power spectrum is obtained by time-averaging the power present in the normal modes of the thermal fluctuations. Flickering spectroscopy has been used extensively on RBCs, but has so far been very low throughput and with some technical limitations. Here we address issues related to active versus passive fluctuations, focusing and optics, camera exposure and sampling, and fast contour detection. In combination with an automated imaging system it is possible to measure thousands of cells in one day, with no user input. We validate this new pipeline by chemical modification of RBC mechanics, and by comparison with simulated fluctuations including each confounding effect. The methods and codes for this robust flickering analysis will allow consistent measurements across labs.
ER  -