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PMID: 2349234 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Liquid crystal domains and thixotropy of filamentous actin suspensions.

Kerst A, Chmielewski C, Livesay C, Buxbaum RE, Heidemann SR

Abstract

The thixotropic properties of filamentous actin suspensions were examined by a step-function shearing protocol. Samples of purified filamentous actin were sheared at 0.2 sec-1 in a cone and plate rheometer. We noted a sharp stress overshoot upon the initiation of shear, indicative of a gel state, and a nearly instantaneous drop to zero stress upon cessation of shear. Stress-overshoot recovery was almost complete after 5 min of "rest" before samples were again sheared at 0.2 sec-1. Overshoot recovery increased linearly with the square root of rest time, suggesting that gel-state recovery is diffusion limited. Actin suspensions subjected to oscillatory shearing at frequencies from 0.003 to 30 radians/sec confirmed the existence of a 5-min time scale in the gel, similar to that for stress-overshoot recovery. Flow of filamentous actin was visualized by polarized light observations. Actin from 6 mg/ml to 20 mg/ml showed the "polycrystalline" texture of birefringence typical for liquid crystal structure. At shear rates less than 1 sec-1, flow occurred by the relative movement of irregular, roughly ellipsoidal actin domains 40-140 microns long; the appearance was similar to moving ice floes. At shear rates greater than 1 sec-1, domains decreased in size, possibly by frictional interactions among domains. Eventually domains flow in a "river" of actin aligned by the flow. Our observations confirm our previous domain-friction model for actin rheology. The similarities between the unusual flow properties of actin and cytoplasm argue that cytoplasm also may flow as domains.

MeSH Terms
Actins Animals Chemical Phenomena Chemistry, Physical Crystallography Elasticity In Vitro Techniques Rabbits Rheology Viscosity
Chemicals
Actins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kerst A
Department of Physiology, Michigan State University, East Lansing 48824.
Chmielewski C
Livesay C
Buxbaum R E
Heidemann S R
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1990-06-00
Pages
4241-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC54084
Subset
IM
Grants
NIGMS NIH HHS · GM 36894 · United States
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