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Thorsten Erdmann

Publications and source records attributed to Thorsten Erdmann.

4 recordsLinked to original sources

Bistability of cell-matrix adhesions resulting from nonlinear receptor-ligand dynamics.

Bistability is a major mechanism for cellular decision making and usually results from positive feedback in biochemical control systems. Here we show theoretically that bistability between unbound and bound states of adhesion clusters results from positive feedback mediated by structural rather than biochemical processes, namely by receptor-ligand dissociation and association dynamics that depend nonlinearly on mechanical force and receptor-ligand separation. For small cell-matrix adhesions, we find rapid switching between unbound and bound states, which in the initial stages of adhesion allows the cell to explore its environment through many transient adhesions.

Cell-Matrix Junctions↗

Focal adhesions as mechanosensors: the two-spring model.

Adhesion-dependent cells actively sense the mechanical properties of their environment through mechanotransductory processes at focal adhesions, which are integrin-based contacts connecting the extracellular matrix to the cytoskeleton. Here we present first steps towards a quantitative understanding of focal adhesions as mechanosensors. It has been shown experimentally that high levels of force are related to growth of and signaling at focal adhesions. In particular, activation of the small GTPase Rho through focal adhesions leads to the formation of stress fibers. Here we discuss one way in which force might regulate the internal state of focal adhesions, namely by modulating the internal rupture dynamics of focal adhesions. A simple two-spring model shows that the stiffer the environment, the more efficient cellular force is built up at focal adhesions by molecular motors interacting with the actin filaments.

Animals↗

Stochastic dynamics of adhesion clusters under shared constant force and with rebinding.

Single receptor-ligand bonds have finite lifetimes, so that biological systems can dynamically react to changes in their environment. In cell adhesion, adhesion bonds usually act cooperatively in adhesion clusters. Outside the cellular context, adhesion clusters can be probed quantitatively by attaching receptors and ligands to opposing surfaces. Here we present a detailed theoretical analysis of the stochastic dynamics of a cluster of parallel bonds under shared constant loading and with rebinding. Analytical solutions for the appropriate one-step master equation are presented for special cases, while the general case is treated with exact stochastic simulations. If the completely dissociated state is modeled as an absorbing boundary, mean cluster lifetime is finite and can be calculated exactly. We also present a detailed analysis of fluctuation effects and discuss various approximations to the full stochastic description.

Journal Article↗

Phase behavior and structure of Janus fluids.

The equilibrium phase behavior of Janus fluids is examined based on a model potential for the interaction between their constituents. Janus fluids consist of axisymmetric particles possessing two different "faces," e.g., one hydrophobic and one hydrophilic surface, and the interaction depends on the relative orientation. Starting from a short range, isotropic potential we make an ansatz for an anisotropic model interaction potential. Two types of symmetries of the particles are considered. One leads to a polar phase. The Helmholtz free energy and the pressure are calculated by the help of an augmented van der Waals approximation. A qualitative phase diagram is obtained. The appearance of a polar phase and the corresponding transition temperature are examined adapting a Landau-de Gennes expansion of the orientational part of the free energy. Monte Carlo simulations are performed and the results are compared with the ones obtained by the analytical description.

Journal Article↗