Communications Biology (Apr 2023)

Morphological profiling by high-throughput single-cell biophysical fractometry

  • Ziqi Zhang,
  • Kelvin C. M. Lee,
  • Dickson M. D. Siu,
  • Michelle C. K. Lo,
  • Queenie T. K. Lai,
  • Edmund Y. Lam,
  • Kevin K. Tsia

DOI
https://doi.org/10.1038/s42003-023-04839-6
Journal volume & issue
Vol. 6, no. 1
pp. 1 – 13

Abstract

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Abstract Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cell-based assays, fractal analysis with single-cell precision remains largely unexplored. To close this gap, here we develop an image-based approach that quantifies a multitude of single-cell biophysical fractal-related properties at subcellular resolution. Taking together with its high-throughput single-cell imaging performance (~10,000 cells/sec), this technique, termed single-cell biophysical fractometry, offers sufficient statistical power for delineating the cellular heterogeneity, in the context of lung-cancer cell subtype classification, drug response assays and cell-cycle progression tracking. Further correlative fractal analysis shows that single-cell biophysical fractometry can enrich the standard morphological profiling depth and spearhead systematic fractal analysis of how cell morphology encodes cellular health and pathological conditions.