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Polyglutamylation of atlantic cod tubulin: immunochemical localization and possible role in pigment granule transport.

Klotz, A (författare)
Gothenburg University,Göteborgs universitet,Zoologiska institutionen,Department of Zoology
Rutberg, M (författare)
Gothenburg University,Göteborgs universitet,Zoologiska institutionen,Department of Zoology
Denoulet, P (författare)
visa fler...
Wallin, Margareta, 1952 (författare)
Gothenburg University,Göteborgs universitet,Zoologiska institutionen,Department of Zoology
visa färre...
 (creator_code:org_t)
1999
1999
Engelska.
Ingår i: Cell motility and the cytoskeleton. - 0886-1544. ; 44:4, s. 263-73
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In higher organisms, there is a large variety of tubulin isoforms, due to multiple tubulin genes and extensive post-translational modification. The properties of microtubules may be modulated by their tubulin isoform composition. Polyglutamylation is a post-translational modification that is thought to influence binding of both structural microtubule associated proteins (MAPs) and mechano-chemical motors to tubulin. The present study investigates the role of tubulin polyglutamylation in a vesicle transporting system, cod (Gadus morhua) melanophores. We did this by microinjecting an antibody against polyglutamylated tubulin into these cells. To put our results into perspective, and to be able to judge their universal application, we characterized cod tubulin polyglutamylation by Western blotting technique, and compared it to what is known from mammals. We found high levels of polyglutamylation in tissues and cell types whose functions are highly dependent on interactions between microtubules and motor proteins. Microinjection of the anti-polyglutamylation antibody GT335 into cultured melanophores interfered with pigment granule dispersion, while dynein-dependent aggregation was unaffected. Additional experiments showed that GT335-injected cells were able to aggregate pigment even when actin filaments were depolymerized, indicating that the maintained ability of pigment aggregation in these cells was indeed microtubule-based and did not depend upon actin filaments. The results indicate that dynein and the kinesin-like dispersing motor protein in cod melanophores bind to tubulin on slightly different sites, and perhaps depend differentially on polyglutamylation for their interaction with microtubules. The binding site of the dispersing motor may bind directly to the polyglutamate chain, or more closely than dynein.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Animals
Antibodies
pharmacology
Bicyclo Compounds
Heterocyclic
pharmacology
Biological Transport
drug effects
Blotting
Western
Brain
metabolism
Cells
Cultured
Chromatophores
metabolism
Dyneins
metabolism
Fishes
metabolism
Immunohistochemistry
Kinesin
metabolism
Microtubules
metabolism
Pigments
Biological
metabolism
Polyglutamic Acid
immunology
metabolism
Thiazoles
pharmacology
Thiazolidines
Tissue Distribution
Tubulin
immunology
metabolism

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Av författaren/redakt...
Klotz, A
Rutberg, M
Denoulet, P
Wallin, Margaret ...
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Biologi
och Biokemi och mole ...
Artiklar i publikationen
Cell motility an ...
Av lärosätet
Göteborgs universitet

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