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Steckhahn, D.

Publications and source records attributed to Steckhahn, D..

2 recordsLinked to original sources

Feedback between filament spacing, crosslinker binding, and self-organization in cytoskeletal bundles

The lateral spacing between filaments in crosslinked cytoskeletal bundles is a critical yet poorly understood physical parameter that affects force generation, transport, and bundle architecture. We develop a biophysical model of crosslinkers and crosslinking motors on filament pairs. Motor/crosslinker binding sets the filament spacing, which in turn biases which motors/crosslinkers can bind. Crosslinking motors generate pulling forces that bring antiparallel filaments closer together, while non-motor crosslinkers with a preferred binding angle exert repulsive torques that maintain larger spacing. We demonstrate these principles in a model of the fission yeast anaphase mitotic spindle midzone, where microtubules form a square array with nearest-neighbor spacing 2-5 times smaller than the length of crosslinking proteins. Our model shows that motor-crosslinker interactions alone are sufficient to drive self-organization into this experimentally observed geometry. Furthermore, the feedback between geometry and binding creates strong indirect cooperativity, because crosslinkers establish spacing that favors binding of similar-length proteins, leading to history-dependent states that persist long after individual protein binding equilibration. This feedback mechanism in which crosslinkers control geometry and geometry controls crosslinker binding should operate in any multi-crosslinker-filament system and represents a general self-organizing principle for cytoskeletal networks.

biophysics↗

PRC1 resists microtubule sliding in two distinct resistive modes due to variations in the separation between overlapping microtubules

Crosslinked cytoskeletal filament networks provide cells with a mechanism to regulate cellular mechanics and force transmission. An example in the microtubule cytoskeleton is mitotic spindle elongation. The three-dimensional geometry of these networks, including the overlap length and lateral microtubule spacing, likely controls how forces can be regulated, but how these parameters evolve during filament sliding is unknown. Recent evidence suggests that the crosslinker PRC1 can resist microtubule sliding by two distinct modes: a braking mode and a less resistive coasting mode. To explore how molecular-scale mechanisms influence network geometry in this system, we developed a computational model of sliding microtubule pairs crosslinked by PRC1 that reproduces the experimentally observed braking and coasting modes. Surprisingly, we found that the braking mode was associated with a substantially smaller lateral separation between the crosslinked microtubules than the coasting mode. This closer separation aligns the PRC1-mediated forces against sliding, increasing the resistive PRC1 force and dramatically reducing sliding speed. The model also finds an emergent similar average sliding speed due to PRC1 resistance, because higher initial sliding speed favors the transition to braking. Together, our results highlight the importance of the three-dimensional geometric relationships between crosslinkers and microtubules.

biophysics↗