Abstract
The thermally driven dynamics of a polymer network are studied by direct
view observation of the motion of a single point within a single
polymer. Taking advantage of rather rigid biological microtubules as a
case study, we expand the space and time scales of the system to those
accessible by optical microscopy and standard video tools. Tracking is
achieved by chemically attaching an optically resolved micro-sphere to a
single point on the filament. We measure a sequence of instantaneous
positions, from which we compute the mean squared displacement vs time.
Typical behavior in a network shows two distinct regimes. At short
times, we observe anomalous diffusion with power law 3/4. At long times
(seconds) the undulation amplitude saturates as a consequence of the
finite length of the polymer. In the network, entanglements effectively
divide the filament into segments shorter than the physical length. In a
pre-stressed network we find a short time sub-diffusive regime with
power law 0.4-0.5, interpreted as a signature of tension along the
individual filament.
Original language | English |
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Title of host publication | American Physical Society, Annual March Meeting, March 16-20, 1998 Los Angeles, CA |
State | Published - 1 Mar 1998 |
Externally published | Yes |