Literature DB >> 3428260

An oscillatory mode for microtubule assembly.

F Pirollet1, D Job, R L Margolis, J R Garel.   

Abstract

Depending upon the conditions under which polymerization takes place, pure tubulin can assemble into microtubules following either the usual monotonic kinetics or a more complex oscillatory mechanism. When present, these oscillations involve large cyclic changes in the extent of polymer formed before a steady-state is reached. Analysis of the microtubules formed at different times shows that these oscillations involve marked redistribution in both the length and number of microtubules. No significant difference is found between two populations of microtubules corresponding to the same level of assembly, one for which the extent of polymerization will remain stable with time and one for which it will decrease by as much as 90% in the next oscillation. The amplitude of these oscillations is sensitive to changes in the concentrations of protein, nucleotide (GTP, GDP or GMPpNp), magnesium ion or GTP regenerating system. A complete shift from an oscillatory to a monotonic polymerization can be induced by a minor increase in the concentration of free nucleotide, GTP or GDP.

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Year:  1987        PMID: 3428260      PMCID: PMC553776          DOI: 10.1002/j.1460-2075.1987.tb02642.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  17 in total

1.  Role of nucleotides in tubulin polymerization: effect of guanylyl 5'-methylenediphosphonate.

Authors:  I V Sandoval; E MacDonald; J L Jameson; P Cuatrecasas
Journal:  Proc Natl Acad Sci U S A       Date:  1977-11       Impact factor: 11.205

2.  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

3.  Differentiation between dynamic instability and end-to-end annealing models for length changes of steady-state microtubules.

Authors:  M Caplow; J Shanks; B P Brylawski
Journal:  J Biol Chem       Date:  1986-12-05       Impact factor: 5.157

4.  Turbidimetric studies of the in vitro assembly and disassembly of porcine neurotubules.

Authors:  F Gaskin; C R Cantor; M L Shelanski
Journal:  J Mol Biol       Date:  1974-11-15       Impact factor: 5.469

Review 5.  In vitro assembly of cytoplasmic microtubules.

Authors:  S N Timasheff; L M Grisham
Journal:  Annu Rev Biochem       Date:  1980       Impact factor: 23.643

6.  Isolation of bovine brain microtubule protein without glycerol: polymerization kinetics change during purification cycles.

Authors:  C F Asnes; L Wilson
Journal:  Anal Biochem       Date:  1979-09-15       Impact factor: 3.365

7.  Isolation from bovine brain of a superstable microtubule subpopulation with microtubule seeding activity.

Authors:  D Job; R L Margolis
Journal:  Biochemistry       Date:  1984-06-19       Impact factor: 3.162

8.  Microtubule assembly nucleated by isolated centrosomes.

Authors:  T Mitchison; M Kirschner
Journal:  Nature       Date:  1984 Nov 15-21       Impact factor: 49.962

9.  A rapid filtration assay for analysis of microtubule assembly, disassembly, and steady-state tubulin flux.

Authors:  L Wilson; K B Synder; W C Thompson; R L Margolis
Journal:  Methods Cell Biol       Date:  1982       Impact factor: 1.441

10.  Reversible binding of Pi by beef heart mitochondrial adenosine triphosphatase.

Authors:  H S Penefsky
Journal:  J Biol Chem       Date:  1977-05-10       Impact factor: 5.157

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  16 in total

1.  Microtubule assembly and oscillations induced by flash photolysis of caged-GTP.

Authors:  A Marx; A Jagla; E Mandelkow
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

2.  Hourglass model for a protein-based circadian oscillator.

Authors:  Eldon Emberly; Ned S Wingreen
Journal:  Phys Rev Lett       Date:  2006-01-24       Impact factor: 9.161

3.  Kinetics of the spontaneous organization of microtubules in solution.

Authors:  M Somers; Y Engelborghs
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

4.  The susceptibility of pure tubulin to high magnetic fields: a magnetic birefringence and x-ray fiber diffraction study.

Authors:  W Bras; G P Diakun; J F Díaz; G Maret; H Kramer; J Bordas; F J Medrano
Journal:  Biophys J       Date:  1998-03       Impact factor: 4.033

5.  A Landau-Ginzburg Model of the Co-existence of Free Tubulin and Assembled Microtubules in Nucleation and Oscillations Phenomena.

Authors:  D Sept; J A Tuszyńskit
Journal:  J Biol Phys       Date:  2000-03       Impact factor: 1.365

6.  Microtubule Dynamics may Embody a Stationary Bipolarity Forming Mechanism Related to the Prokaryotic Division Site Mechanism (Pole-to-Pole Oscillations).

Authors:  A Hunding
Journal:  J Biol Phys       Date:  2004-01       Impact factor: 1.365

7.  Models of assembly and disassembly of individual microtubules: stochastic and averaged equations.

Authors:  H Bolterauer; H J Limbach; J A Tuszyński
Journal:  J Biol Phys       Date:  1999-03       Impact factor: 1.365

8.  Dynamics of microtubules from erythrocyte marginal bands.

Authors:  B Trinczek; A Marx; E M Mandelkow; D B Murphy; E Mandelkow
Journal:  Mol Biol Cell       Date:  1993-03       Impact factor: 4.138

9.  Visualization of glucocorticoid receptor translocation and intranuclear organization in living cells with a green fluorescent protein chimera.

Authors:  H Htun; J Barsony; I Renyi; D L Gould; G L Hager
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

10.  A multistranded polymer model explains MinDE dynamics in E. coli cell division.

Authors:  Eric N Cytrynbaum; Brandon D L Marshall
Journal:  Biophys J       Date:  2007-05-04       Impact factor: 4.033

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