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Probing short-range protein Brownian motion in the cytoplasm of living cells
Probing short-range protein Brownian motion in the cytoplasm of living cells
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Probing short-range protein Brownian motion in the cytoplasm of living cells
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Probing short-range protein Brownian motion in the cytoplasm of living cells
Probing short-range protein Brownian motion in the cytoplasm of living cells
Journal Article

Probing short-range protein Brownian motion in the cytoplasm of living cells

2014
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Overview
The translational motion of molecules in cells deviates from what is observed in dilute solutions. Theoretical models provide explanations for this effect but with predictions that drastically depend on the nanoscale organization assumed for macromolecular crowding agents. A conclusive test of the nature of the translational motion in cells is missing owing to the lack of techniques capable of probing crowding with the required temporal and spatial resolution. Here we show that fluorescence-fluctuation analysis of raster scans at variable timescales can provide this information. By using green fluorescent proteins in cells, we measure protein motion at the unprecedented timescale of 1 μs, unveiling unobstructed Brownian motion from 25 to 100 nm, and partially suppressed diffusion above 100 nm. Furthermore, experiments on model systems attribute this effect to the presence of relatively immobile structures rather than to diffusing crowding agents. We discuss the implications of these results for intracellular processes. Models for protein diffusion in cells assume a large macromolecular crowding effect. Here Di Rienzo et al. visualize GFP diffusion at the millisecond timescale to observe unobstructed Brownian motion in mammalian cells for distances up to 100 nm, revealing minimal influence of macromolecular crowding.