Data-driven analysis for the evaluation of cortical mechanics of non-adherent cells

Atomic Force Microscopy (AFM) analysis of single cells, especially nonadherent, is inherently slow and analysis-heavy. To address the inherent difficulty of measuring individual cells, and to scale up toward a large number of cells, we take a two-fold approach; first, we introduce an easy-to-fabricate reusable poly(dimethylsiloxane)-based array that consists of micron-sized traps for single-cell trapping, second, we apply a deep-learning method directly on the extracted curves to facilitate and automate the analysis. Our approach is validated using suspended cells, and by applying a small compression with a tipless cantilever AFM probe, we investigate the effect of various cytoskeletal drugs on their deformability. We then apply deep learning models to extract the elasticity of the cell directly from the raw data (with a Coefficient of Determination of 0.47) as well as for binary (with an Area Under the Curve score of 0.91) and multi-class classification (with accuracy scores exceeding 0.9 for each drug). Overall, the versatility to fabricate the microwells in conjunction with the automated analysis and classification streamline the analysis process and demonstrate their ability to generalize to other tasks, such as drug detection.

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Publication Details

Journal
Scientific Reports
Published
2025-03-20
DOI
https://doi.org/10.1038/s41598-025-94315-4
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Data-driven analysis for the evaluation of cortical mechanics of non-adherent cells

Vincent Chan, Cyril Aubry, Shaohong Luo, Jeremy C. M. Teo et al.
Scientific Reports
Cellular Mechanics and Interactions
article

Data-driven analysis for the evaluation of cortical mechanics of non-adherent cells

Vincent Chan, Cyril Aubry, Shaohong Luo, Jeremy C. M. Teo, Sarah Alkhatib, Nicholas Hallfors, Jiranuwat Sapudom, Anna‐Maria Pappa, Cesare Stefanini, Leontios J. Hadjileontiadis, Charalampos Lamprou, Jawaher Alhammadi
article en

Abstract

Atomic Force Microscopy (AFM) analysis of single cells, especially nonadherent, is inherently slow and analysis-heavy. To address the inherent difficulty of measuring individual cells, and to scale up toward a large number of cells, we take a two-fold approach; first, we introduce an easy-to-fabricate reusable poly(dimethylsiloxane)-based array that consists of micron-sized traps for single-cell trapping, second, we apply a deep-learning method directly on the extracted curves to facilitate and automate the analysis. Our approach is validated using suspended cells, and by applying a small compression with a tipless cantilever AFM probe, we investigate the effect of various cytoskeletal drugs on their deformability. We then apply deep learning models to extract the elasticity of the cell directly from the raw data (with a Coefficient of Determination of 0.47) as well as for binary (with an Area Under the Curve score of 0.91) and multi-class classification (with accuracy scores exceeding 0.9 for each drug). Overall, the versatility to fabricate the microwells in conjunction with the automated analysis and classification streamline the analysis process and demonstrate their ability to generalize to other tasks, such as drug detection.

Scientific ReportsVol. 15(1)
Scuola Superiore Sant'Anna (IT), Khalifa University of Science and Technology (AE), Aristotle University of Thessaloniki (GR), Technology Innovation Institute (AE), Biotechnology Research Center (IR)
Al Jalila Foundation, New York University Abu Dhabi, Khalifa University of Science, Technology and Research
Good health and well-being
Openalex Percentile: Top 94%
Cellular Mechanics and Interactions
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