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Sökning: id:"swepub:oai:gup.ub.gu.se/114023" > Dependency of micro...

Dependency of microtubule-associated proteins (MAPs) for tubulin stability and assembly; use of estramustine phosphate in the study of microtubules.

Fridén, B (författare)
Gothenburg University,Göteborgs universitet,Zoologiska institutionen,Department of Zoology
Wallin, Margareta, 1952 (författare)
Gothenburg University,Göteborgs universitet,Zoologiska institutionen,Department of Zoology
 (creator_code:org_t)
1991
1991
Engelska.
Ingår i: Molecular and cellular biochemistry. - 0300-8177. ; 105:2, s. 149-58
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Microtubule-associated proteins (MAPs) were separated from tubulin with several different methods. The ability of the isolated MAPs to reinduce assembly of phosphocellulose purified tubulin differed markedly between the different methods. MAPs isolated by addition of 0.35 M NaCl to taxol-stabilized microtubules stimulated tubulin assembly most effectively, while addition of 0.6 M NaCl produced MAPs with a substantially lower ability to stimulate tubulin assembly. The second best preparation was achieved with phosphocellulose chromatographic separation of MAPs with 0.6 M NaCl elution. The addition of estramustine phosphate to microtubules reconstituted of MAPs prepared by 0.35 M NaCl or phosphocellulose chromatography, induced less disassembly than for microtubules assembled from unseparated proteins, and was almost without effect on microtubules reconstituted from MAPs prepared by taxol and 0.6 M NaCl. Estramustine phosphate binds to the tubulin binding part of the MAPs, and the results do therefore indicate that the MAPs are altered by the separation methods. Since the MAPs are regarded as highly stable molecules, one probable alteration could be aggregation of the MAPs, as also indicated by the results. The purified tubulin itself seemed not to be affected by the phosphocellulose purification, since the microtubule proteins were unchanged by the low buffer strenght used during the cromatography. However, the assembly competence after a prolonged incubation of the microtubule proteins at 4 degrees C was dependent on intact bindings between the tubulin and MAPs.

Ämnesord

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

Nyckelord

Alkaloids
pharmacology
Animals
Brain Chemistry
Cattle
Electrophoresis
Polyacrylamide Gel
Estramustine
metabolism
pharmacology
Microtubule-Associated Proteins
chemistry
isolation & purification
metabolism
Microtubules
chemistry
drug effects
ultrastructure
Paclitaxel
Tubulin
metabolism

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Fridén, B
Wallin, Margaret ...
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NATURVETENSKAP
NATURVETENSKAP
och Biologi
och Biokemi och mole ...
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Molecular and ce ...
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Göteborgs universitet

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