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Friday February 22, 4pm, Phillips 332
(refreshments served in Phillips 330 starting at 3:30)
Abstract:
The mechanics of the in vivo cytoskeleton is controlled in part by the
details of its non-equilibrium steady-state. In this ``active'' material,
molecular motors (e.g. myosin) exert transient contractile stresses on the
F-actin filament network. Since microrheology traditionally relies of the
linear response properties of the soft materials in thermal equilibrium,
this departure from equilibrium has profound implications for the
interpretation of microrheological data from the interior of living cells
and in vitro active networks. In active networks, such as the in vitro
systems of Mizuno et al. [Science 315 (5810) pp. 370-373 (2007).] and in
living cells, the underlying theoretical foundation of the interpretation of
microrheology -- the Fluctuation-Dissipation theorem -- does not apply. New
ideas are needed.
In this talk, I review microrheology, and then discuss a new theoretical
interpretation of microrheology in active (i.e. molecular motor driven)
networks. I also explore how molecular motor activity can reversibly control
the elastic properties of these active gels. The cytoskeleton points towards
the development of new biomimetic materials whose elastic properties can be
tuned by controlling the material's non-equilibrium steady-state.
Department of Mathematics | CB 3250 Phillips Hall | University of North Carolina at Chapel Hill | Chapel Hill, NC 27599