Simulation-based Reconstructed Diffusion unveils the effect of aging on protein diffusion in Escherichia coli

PLoS Comput Biol. 2023 Sep 11;19(9):e1011093. doi: 10.1371/journal.pcbi.1011093. eCollection 2023 Sep.

Abstract

We have developed Simulation-based Reconstructed Diffusion (SbRD) to determine diffusion coefficients corrected for confinement effects and for the bias introduced by two-dimensional models describing a three-dimensional motion. We validate the method on simulated diffusion data in three-dimensional cell-shaped compartments. We use SbRD, combined with a new cell detection method, to determine the diffusion coefficients of a set of native proteins in Escherichia coli. We observe slower diffusion at the cell poles than in the nucleoid region of exponentially growing cells, which is independent of the presence of polysomes. Furthermore, we show that the newly formed pole of dividing cells exhibits a faster diffusion than the old one. We hypothesize that the observed slowdown at the cell poles is caused by the accumulation of aggregated or damaged proteins, and that the effect is asymmetric due to cell aging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Shape
  • Cellular Senescence*
  • Computer Simulation
  • Escherichia coli*

Grants and funding

The research was funded by the EU Marie-Curie ITN project SynCrop (project number 764591; salary of LM), ERC Advanced grant “ABCVolume” (grant number 670578; salary of WMS) and the NWO National Science Program “The limits to growth” (grant number NWA.1292.19.170; salary of DSL), all grants awarded to BP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.