Literature DB >> 337490

Immunofluorescence localization of proteins of high molecular weight along intracellular microtubules.

P Sherline, K Schiavone.   

Abstract

To help clarify the role, in cytoplasmic microtubule function, of the proteins of high molecular weight that coassemble with tubulin in vitro, a monospecific antibody against the proteins of high molecular weight was prepared from the serum of immunized rabbits by affinity chromatography. With indirect immunofluorescence we found that the protein in both cultured neuroblastoma cells and 3T3 cells in distributed in an extensive filamentous array that originates at sites near the nucleus and extends to the cell periphery or, in neuroblastoma cells, gathers into bundles which enter neurites. No filaments were seen with nonspecific antibodies from serum taken before immunization, and prior incubation of the specific antibody with purified protein of high molecular weight (but not tubulin) prevented filament visualization. The filamentous pattern in 3T3 cells was disrupted by colchicine. This evidence indicates that the proteins of high molecular weight are found in cells in association with cytoplasmic microtubules.

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Year:  1977        PMID: 337490     DOI: 10.1126/science.337490

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  29 in total

1.  Reply: A MAP by Any Other Name Would Still Bind to Microtubules.

Authors:  N. A. Durso; R. J. Cyr
Journal:  Plant Cell       Date:  1994-12       Impact factor: 11.277

2.  Microtubule Binding Proteins Are Not Necessarily Microtubule-Associated Proteins.

Authors:  L. C. Morejohn
Journal:  Plant Cell       Date:  1994-12       Impact factor: 11.277

3.  Self-assembly of microtubules in extracts of cultured HeLa cells and the identification of HeLa microtubule-associated proteins.

Authors:  J C Bulinski; G G Borisy
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

4.  Microtubule-associated proteins (MAPs): a monoclonal antibody to MAP 1 decorates microtubules in vitro but stains stress fibers and not microtubules in vivo.

Authors:  D J Asai; W C Thompson; L Wilson; C F Dresden; H Schulman; D L Purich
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

5.  High molecular weight polypeptides (270,000-340,000) from cultured cells are related to hog brain microtubule-associated proteins but copurify with intermediate filaments.

Authors:  R Pytela; G Wiche
Journal:  Proc Natl Acad Sci U S A       Date:  1980-08       Impact factor: 11.205

6.  Widespread occurrence of polypeptides related to neurotubule-associated proteins (MAP-1 and MAP-2) in non-neuronal cells and tissues.

Authors:  G Wiche; E Briones; C Koszka; U Artlieb; R Krepler
Journal:  EMBO J       Date:  1984-05       Impact factor: 11.598

7.  Differential distribution of microtubule-associated proteins MAP-1 and MAP-2 in neurons of rat brain and association of MAP-1 with microtubules of neuroblastoma cells (clone N2A).

Authors:  G Wiche; E Briones; H Hirt; R Krepler; U Artlieb; H Denk
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

Review 8.  Microtubule-associated proteins: subunits of the cytomatrix.

Authors:  R B Vallee; G S Bloom; W E Theurkauf
Journal:  J Cell Biol       Date:  1984-07       Impact factor: 10.539

9.  Nerve growth factor regulates both the phosphorylation and steady-state levels of microtubule-associated protein 1.2 (MAP1.2).

Authors:  J M Aletta; S A Lewis; N J Cowan; L A Greene
Journal:  J Cell Biol       Date:  1988-05       Impact factor: 10.539

10.  Association of microtubule-associated protein 2 (MAP 2) with microtubules and intermediate filaments in cultured brain cells.

Authors:  G S Bloom; R B Vallee
Journal:  J Cell Biol       Date:  1983-06       Impact factor: 10.539

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