Literature DB >> 3700474

Subaxolemmal cytoskeleton in squid giant axon. I. Biochemical analysis of microtubules, microfilaments, and their associated high-molecular-weight proteins.

T Kobayashi, S Tsukita, S Tsukita, Y Yamamoto, G Matsumoto.   

Abstract

Using the squid giant axon, we analyzed biochemically the molecular organization of the axonal cytoskeleton underlying the axolemma (subaxolemmal cytoskeleton). The preparation enriched in the subaxolemmal cytoskeleton was obtained by squeezing out the central part of the axoplasm using a roller. The electrophoretic banding pattern of the subaxolemmal cytoskeleton was characterized by large amounts of two high-molecular-weight (HMW) proteins (260 and 255 kD). The alpha, beta-tubulin, actin, and some other proteins were also its major constituents. The 260-kD protein is known to play an important role in maintaining the excitability of the axolemma (Matsumoto, G., M. Ichikawa, A. Tasaki, H. Murofushi, and H. Sakai, 1983, J. Membr. Biol., 77:77-91) and was recently designated "axolinin" (Sakai, H., G. Matsumoto, and H. Murofushi, 1985, Adv. Biophys., 19:43-89). We purified axolinin and the 255-kD protein in their native forms and further characterized their biochemical properties. The purified axolinin was soluble in 0.6 M NaCl solution but insoluble in 0.1 M NaCl solution. It co-sedimented with microtubules but not with actin filaments. In low-angle rotary-shadowing electron microscopy, the axolinin molecule in 0.6 M NaCl solution looked like a straight rod approximately 105 nm in length with a globular head at one end. On the other hand, the purified 255-kD protein was soluble in both 0.1 and 0.6 M NaCl solution and co-sedimented with actin filaments but not with microtubules. The 255-kD protein molecule appeared as a characteristic horseshoe-shaped structure approximately 35 nm in diameter. Furthermore, the 255-kD protein showed no cross-reactivity to the anti-axolinin antibody. Taken together, these characteristics lead us to conclude that the subaxolemmal cytoskeleton in the squid giant axon is highly specialized, and is mainly composed of microtubules and a microtubule-associated HMW protein (axolinin), and actin filaments and an actin filament-associated HMW protein (255-kD protein).

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Year:  1986        PMID: 3700474      PMCID: PMC2114230          DOI: 10.1083/jcb.102.5.1699

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  32 in total

1.  Transportation and maintenance of adult squid (Doryteuthis bleekeri) for physiological studies.

Authors:  G Matsumoto
Journal:  Biol Bull       Date:  1976-04       Impact factor: 1.818

2.  Chromatography of myosin on diethylaminoethyl-Sephadex A-50.

Authors:  E G Richards; C S Chung; D B Menzel; H S Olcott
Journal:  Biochemistry       Date:  1967-02       Impact factor: 3.162

3.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

4.  The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin.

Authors:  J A Spudich; S Watt
Journal:  J Biol Chem       Date:  1971-08-10       Impact factor: 5.157

5.  Microtubule assembly in the absence of added nucleotides.

Authors:  M L Shelanski; F Gaskin; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  1973-03       Impact factor: 11.205

6.  Bundling of microtubules in vitro by a high molecular weight protein prepared from the squid axon.

Authors:  H Murofushi; Y Minami; G Matsumoto; H Sakai
Journal:  J Biochem       Date:  1983-02       Impact factor: 3.387

7.  Actin is the naturally occurring inhibitor of deoxyribonuclease I.

Authors:  E Lazarides; U Lindberg
Journal:  Proc Natl Acad Sci U S A       Date:  1974-12       Impact factor: 11.205

8.  Binding sites of calmodulin and actin on the brain spectrin, calspectin.

Authors:  S Tsukita; S Tsukita; H Ishikawa; M Kurokawa; K Morimoto; K Sobue; S Kakiuchi
Journal:  J Cell Biol       Date:  1983-08       Impact factor: 10.539

9.  Monomer-polymer equilibria in the axon: direct measurement of tubulin and actin as polymer and monomer in axoplasm.

Authors:  J R Morris; R J Lasek
Journal:  J Cell Biol       Date:  1984-06       Impact factor: 10.539

10.  Release of proteins from the inner surface of squid axon membrane labeled with tritiated N-ethylmaleimide.

Authors:  I Inoue; H C Pant; I Tasaki; H Gainer
Journal:  J Gen Physiol       Date:  1976-10       Impact factor: 4.086

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  4 in total

1.  Interfacial models of nerve fiber cytoskeleton.

Authors:  V V Malev; D B Gromov; M S Brudnaya
Journal:  Biophys J       Date:  1992-10       Impact factor: 4.033

2.  Anticalmodulin drugs block the sodium gating current of squid giant axons.

Authors:  M Ichikawa; M Urayama; G Matsumoto
Journal:  J Membr Biol       Date:  1991-03       Impact factor: 1.843

3.  Subaxolemmal cytoskeleton in squid giant axon. II. Morphological identification of microtubule- and microfilament-associated domains of axolemma.

Authors:  S Tsukita; S Tsukita; T Kobayashi; G Matsumoto
Journal:  J Cell Biol       Date:  1986-05       Impact factor: 10.539

4.  Myosin Va binding to neurofilaments is essential for correct myosin Va distribution and transport and neurofilament density.

Authors:  Mala V Rao; Linda J Engle; Panaiyur S Mohan; Aidong Yuan; Dike Qiu; Anne Cataldo; Linda Hassinger; Stephen Jacobsen; Virginia M-Y Lee; Athena Andreadis; Jean-Pierre Julien; Paul C Bridgman; Ralph A Nixon
Journal:  J Cell Biol       Date:  2002-10-28       Impact factor: 10.539

  4 in total

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