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© The Rockefeller University Press, 0021-9525/2000//635 $5.00
The Journal of Cell Biology, Volume 149, Number 3, , 2000 635-646


Original Article

Isoforms of {alpha}-Actinin from Cardiac, Smooth, and Skeletal Muscle Form Polar Arrays of Actin Filaments



Kenneth A. Taylora, Dianne W. Taylora, and Fred Schachatb

a Institute of Molecular Biophysics, Florida State University, Tallahassee, Florida 32306-3015
b Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710-3011
Institute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306-3015.(850) 561-1406(850) 644-3357

taylor{at}bio.fsu.edu

We have used a positively charged lipid monolayer to form two-dimensional bundles of F-actin cross-linked by {alpha}-actinin to investigate the relative orientation of the actin filaments within them. This method prevents growth of the bundles perpendicular to the monolayer plane, thereby facilitating interpretation of the electron micrographs. Using {alpha}-actinin isoforms isolated from the three types of vertebrate muscle, i.e., cardiac, skeletal, and smooth, we have observed almost exclusively cross-linking between polar arrays of filaments, i.e., actin filaments with their plus ends oriented in the same direction. One type of bundle can be classified as an Archimedian spiral consisting of a single actin filament that spirals inward as the filament grows and the bundle is formed. These spirals have a consistent hand and grow to a limiting internal diameter of 0.4–0.7 µm, where the filaments appear to break and spiral formation ceases. These results, using isoforms usually characterized as cross-linkers of bipolar actin filament bundles, suggest that {alpha}-actinin is capable of cross-linking actin filaments in any orientation. Formation of specifically bipolar or polar filament arrays cross-linked by {alpha}-actinin may require additional factors that either determine the filament orientation or restrict the cross-linking capabilities of {alpha}-actinin.

Key Words: electron microscopy • actinin ultrastructure • actinin metabolism • actins ultrastructure • molecular structure



© 2000 The Rockefeller University Press

Abbreviations used in this paper: 2-D, two-dimensional; 3-D, three-dimensional.



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