Related Experiment Video
Updated: Sep 18, 2025

Quantitative Analysis of Viscoelastic Properties of Red Blood Cells Using Optical Tweezers and Defocusing Microscopy
Published on: March 25, 2022
A Computationally Efficient Viscoelastic Eukaryotic Cell Model
Pietro Miotti1,2, Matteo Scarpone1, Chwee Teck Lim3,4,5
1Institute of Computing, Faculty of Informatics, Università della Svizzera italiana, Lugano, Switzerland.
Purpose:
Modeling eukaryotic cell flow in microfluidic devices and capillary networks can be instrumental in assessing how cell mechanics influence its behavior. Due to the viscoelastic characteristics of cells and their capacity for substantial deformation, models that are both detailed and computationally efficient are necessary to explore cell rheology. We present a coarse-grained model for simulating the mechanics of eukaryotic cells in flow, with a focus on the modeling of cell membrane, nucleus, and cytoskeleton.
Methods:
The cell and nucleus membranes are represented using surface triangulation, capturing both viscous and elastic properties of the membranes. To maintain computational efficiency while retaining the ability to reproduce the viscoelastic behavior of the entire cell, the complexity of the cytoskeleton model is reduced through the use of the viscoelastic bonds. Dissipative Particle Dynamics is employed to facilitate flow simulations; however, the model is suitable for use in many existing continuum and particle-based methods.
Results:
The cell model is calibrated and validated using experimental data from micropipette aspiration and microfluidic experiments involving breast epithelial cells (MCF-10A).
Conclusion:
We believe the balance between simplicity and accuracy makes the proposed model a valuable tool for simulating eukaryotic cell mechanics in flow, enabling faster simulations, while also simplifying the parameterization procedure.
More Related Videos
Related Concept Videos
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Non-equilibrium in the Cell
Adaptability of Cytoskeletal Filaments
Cell-matrix's Response to Mechanical Forces
Anchoring junctions mechanically attach a cell to the...
Elastic Strain Energy for Shearing Stresses
Mechanical Protein Functions

