Literature DB >> 1973093

Kinetics of the spontaneous organization of microtubules in solution.

M Somers1, Y Engelborghs.   

Abstract

Optically anisotropic zones occur spontaneously in solutions of microtubules. These tactoids, in which microtubules are arranged in parallel arrays, can be visualized by their birefringence. With microtubules assembled in the presence of associated proteins (MAPs), birefringence appears immediately after nucleation of polymerization, even at relatively low protein concentrations. It is not dependent on whether the assembly is initiated by temperature jump or by isothermal addition of GTP. With pure tubulin, assembled in buffers containing 25% glycerol or 4% dimethylsulfoxide and/or taxol, birefringence appears within a few hours, but it can be speeded up by gentle agitation. With tubulin assembled in the presence of MAPs, spontaneous orientation occurs simultaneously with polymerization. This may be due to the existence of more pronounced repulsive forces between microtubules when they are covered with MAPs. A simple calculation of the covolume, suggests that tactoid formation is expected for microtubules of lengths of 5 to 10 microns at protein concentrations in the range 1 to 3 mg/ml (as observed), and that repulsive forces will promote tactoid formation at even lower protein concentrations.

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Year:  1990        PMID: 1973093     DOI: 10.1007/bf00183377

Source DB:  PubMed          Journal:  Eur Biophys J        ISSN: 0175-7571            Impact factor:   1.733


  24 in total

1.  A kinetic analysis of the assembly of microtubules in vitro.

Authors:  Y Engelborghs; L C De Maeyer; N Overbergh
Journal:  FEBS Lett       Date:  1977-08-01       Impact factor: 4.124

2.  Comparison of the effects of microtubule-associated protein 2 and tau on the packing density of in vitro assembled microtubules.

Authors:  M M Black
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

3.  Synchronous oscillations in microtubule polymerization.

Authors:  M F Carlier; R Melki; D Pantaloni; T L Hill; Y Chen
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

4.  Sites of microtubule assembly and disassembly in the mitotic spindle.

Authors:  T Mitchison; L Evans; E Schulze; M Kirschner
Journal:  Cell       Date:  1986-05-23       Impact factor: 41.582

5.  Mechanism of microtubule assembly. Changes in polymer structure and organization during assembly of sea urchin egg tubulin.

Authors:  H W Detrich; M A Jordan; L Wilson; R C Williams
Journal:  J Biol Chem       Date:  1985-08-05       Impact factor: 5.157

6.  Kinetic analysis of microtubule self-assembly in vitro.

Authors:  K A Johnson; G G Borisy
Journal:  J Mol Biol       Date:  1977-11-25       Impact factor: 5.469

7.  Spatial patterns from oscillating microtubules.

Authors:  E Mandelkow; E M Mandelkow; H Hotani; B Hess; S C Müller
Journal:  Science       Date:  1989-12-08       Impact factor: 47.728

8.  End-to-end annealing of microtubules in vitro.

Authors:  S W Rothwell; W A Grasser; D B Murphy
Journal:  J Cell Biol       Date:  1986-02       Impact factor: 10.539

9.  Two-phase formation in solutions of tobacco mosaic virus and the problem of long-range forces.

Authors:  G OSTER
Journal:  J Gen Physiol       Date:  1950-05-20       Impact factor: 4.086

10.  Taxol-induced bundling of brain-derived microtubules.

Authors:  P F Turner; R L Margolis
Journal:  J Cell Biol       Date:  1984-09       Impact factor: 10.539

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  1 in total

1.  A model of microtubule oscillations.

Authors:  A Marx; E Mandelkow
Journal:  Eur Biophys J       Date:  1994       Impact factor: 1.733

  1 in total

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