By John H. Hartwig, Richard Niederman, Stuart E. Lind (auth.), Donald B. Roodyn (eds.)
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And Thomas, G. , 1982. Coexistence of vinculin and a vinculin-like protein of higher molecular weight in smooth muse1e, J. Biol. Chem. 257:11024-11031. Fine, R. , and Blitz, A. , 1975, A chemical comparison of tropomyosins from museie and non-muscle tissues, J. Mol. Biol. 95:447-454. Flanagan, M. , 1980, Cytochalasins block actin filament elongation by binding to high affinity sites associated with F-actin, J. Biol. Chem. 255:835-838. , 1953, Prineiples 0/ Polymer Chemistry, Comell University Press, Ithaca, New York.
256:11999-12004. , Lewis, W. , and Smillie, L. , 1978, Non-polymerizability of platelet tropomyosin and its NH 2- and COOH- terminal sequences, FEBS Letters 91:237-241. Cöte, G. , Lewis, W. , Pato, M. , and Smillie, L. , 1978, Platelet tropomyosin: lack of binding to skeletal museIe troponin and correlation with sequence, FEBS Letters 94:131135. Craig, S. , and Powell, L. , 1980, Regulation of actin polymerization by villin, a 95,000dalton cytoskeleton component of intestinal brush borders, Cel/ 22:739-746.
Two proteins, actin-binding protein and a-actinin, participate in the formation of the cortical network seen in leukocytes. The most important crosslinker of leukocytes extracts is actin-binding protein, which accounts for 75% of the cross-linking activity in such extracts. The network is characterized by a striking perpendicularity of branching; the majority of filaments intersect at c10se to a right angle. The network's boundaries can be defined in the light microscope as the c1ear, organelle-free region of hyaline cytoplasm between the plasma membrane and the lysosomes.