Literature DB >> 583496

Specific interaction of cytochalasins with muscle and platelet actin filaments in vitro.

T H Howard, S Lin.   

Abstract

The cytochalasins (CE, CD, CB and H2CB) inhibit numerous cellular processes which require the interaction of actin with other structural and contractile proteins. In this report we describe the effects of the cytochalasins on the viscosity and morphology of muscle and platelet actin. The cytochalasins decreased the viscosity of F-actin solutions. The effect of H2CB, CB and CD ON F-actin viscosity was maximal at concentrations of 20-50 micro M and did not increase with time. In contrast, CE caused a progressive decrease in the viscosity of F-actin solutions which was dependent upon the concentration of CE and the duration of incubation of the CE-actin mixture. After two hours of incubation of drug-actin mixtures, the relative effectiveness of the cytochalasins in reducing the viscosity of F-actin was CE greater than CD greater than CB=H2CB. The effects of CD and CE were paralleled by morphologic changes in negatively stained actin filaments. The effects of the cytochalasins on the viscosity and morphology of muscle and platelet actin were the same whether the drugs were added before or after the polymerization of the protein. These studies show that the interaction of the cytochalasins with actin is highly specific. Because the relative potencies of these drugs for affecting motile processes and the relative affinities of the drugs for binding sites within a variety of cells are CE greater than CD greater than CB=H2CB, the effects of cytochalasins on actin described here may contribute to some of the biological effects of the drugs on motile processes.

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Year:  1979        PMID: 583496     DOI: 10.1002/jss.400110303

Source DB:  PubMed          Journal:  J Supramol Struct        ISSN: 0091-7419


  6 in total

1.  Possible involvement of calmodulin and the cytoskeleton in electrofusion of plant protoplasts.

Authors:  S Abe; J Takeda
Journal:  Plant Physiol       Date:  1986-08       Impact factor: 8.340

2.  The interaction of 6-propionyl-2-(NN-dimethyl)aminonaphthalene (PRODAN)-labelled actin with actin-binding proteins and drugs.

Authors:  K Zechel
Journal:  Biochem J       Date:  1993-03-01       Impact factor: 3.857

3.  Structural and dynamic states of actin in the erythrocyte.

Authors:  J C Pinder; W B Gratzer
Journal:  J Cell Biol       Date:  1983-03       Impact factor: 10.539

4.  Inhibition of actin polymerization by marine toxin pectenotoxin-2.

Authors:  Masatoshi Hori; Futoshi Yazama; Yasuhiro Matsuura; Ryo Yoshimoto; Takeharu Kaneda; Takeshi Yasumoto; Hiroshi Ozaki; Hideaki Karaki
Journal:  J Vet Med Sci       Date:  2017-12-26       Impact factor: 1.267

5.  Cytochalasins inhibit nuclei-induced actin polymerization by blocking filament elongation.

Authors:  D C Lin; K D Tobin; M Grumet; S Lin
Journal:  J Cell Biol       Date:  1980-02       Impact factor: 10.539

6.  Correlation between effects of 24 different cytochalasins on cellular structures and cellular events and those on actin in vitro.

Authors:  I Yahara; F Harada; S Sekita; K Yoshihira; S Natori
Journal:  J Cell Biol       Date:  1982-01       Impact factor: 10.539

  6 in total

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