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Biologische Systeme und Medizin Poster: Mi., 14:00–16:30 M-P188<br />

Protein Diffusion in Biological Cells<br />

Wolfgang Doster 1 , Sebastian Busch 1 , Stephane Longeville 2<br />

1 Technical University Munich, Physics department E 13, D-85748 Garching – 2 LLB<br />

CEA CRNS Saclay 91191, Gif-sur Yvette, France<br />

A characteristic of the interior of cells is the high total concentration of macromolecules.<br />

Such media are termed crowded rather than concentrated since no single<br />

macromolecular species occurs at high concentration. But taken together they occupy<br />

a signifcant fraction (20-30 %) of the total volume. This affects protein diffusion and<br />

protein association equilibria through excluded volume effects (highly non-ideal solutions).<br />

The goal of our project is to understand the effect of protein-protein interactions<br />

on molecular diffusion at high concentration. Our model of crowding in biological cells<br />

is hemoglobin diffusion inside erythrocytes. Using a combination of neutron spin echo<br />

and backscattering spectroscopy with low angle scattering, we analyse the effects of<br />

direct interactions and hydrodynamic interactions. Neutrons scattering allows probing<br />

molecular diffusion on a microscopic scale at high Q. The protein diffusion coefficients<br />

increase with decreasing Q indicating a cross-over from short-time self-diffusion to<br />

collective diffusion. Myoglobin solutions were investigated at various protein concentrations<br />

as well as hemoglobin diffusion in blood cells.

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