Literature DB >> 489611

Colchicine inhibition of microtubule assembly via copolymer formation.

H Sternlicht, I Ringel.   

Abstract

Colchicine.tubulin complex (CD) inhibits microtubule assembly. We examined this inhibition under conditions where spontaneous nucleation was suppressed and assembly was restricted to an elongation polymerization. We found that CD inhibited assembly by a mechanism which preserved the ability of microtubule ends to add tubulin. This observation is inconsistent with the end-poisoning model which recently was proposed as a general mechanism for assembly inhibition by CD. Our data are consistent with the following model: (a) microtubules formed in the presence of CD are CD-tubulin copolymers; (b) these copolymers can have appreciable numbers of incorporated CDs which are, most likely, randomly distributed in the copolymers; (c) CD-tubulin copolymers have assembly-competent ends with association and dissociation rate constants which decrease as the CD/tubulin ratio in the copolymers, (CD/T)MT, increases; and (d) the critical tubulin concentrations required for microtubule assembly increase in the presence of CD, indicating that copolymer affinity for tubulin decreases as (CD/T)MT increases.

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Year:  1979        PMID: 489611

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  25 in total

1.  A kinetic model for colchicine inhibition of microtubule assembly.

Authors:  H Sternlicht; I Ringel; J Szasz
Journal:  Biophys J       Date:  1980-10       Impact factor: 4.033

2.  Kinetic analysis of tubulin assembly in the presence of the microtubule-associated protein TOGp.

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4.  Response of microtubules to the addition of colchicine and tubulin-colchicine: evaluation of models for the interaction of drugs with microtubules.

Authors:  A Vandecandelaere; S R Martin; Y Engelborghs
Journal:  Biochem J       Date:  1997-04-01       Impact factor: 3.857

5.  Enhanced tumor retention of NTSR1-targeted agents by employing a hydrophilic cysteine cathepsin inhibitor.

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Journal:  Eur J Med Chem       Date:  2019-05-25       Impact factor: 6.514

Review 6.  VP16-213 and podophyllotoxin. A study on the relationship between chemical structure and biological activity.

Authors:  J D Loike
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

7.  Respective roles of neurofilaments, microtubules, MAP1B, and tau in neurite outgrowth and stabilization.

Authors:  T B Shea; M L Beermann
Journal:  Mol Biol Cell       Date:  1994-08       Impact factor: 4.138

8.  2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site.

Authors:  R J D'Amato; C M Lin; E Flynn; J Folkman; E Hamel
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

9.  Theory for modeling the copolymerization of tubulin and tubulin-colchicine complex.

Authors:  H Sternlicht; I Ringel; J Szasz
Journal:  Biophys J       Date:  1983-06       Impact factor: 4.033

10.  Podophyllotoxin poisoning of microtubules at steady-state: effect of substoichiometric and superstoichiometric concentrations of drug.

Authors:  R Manso-Martínez
Journal:  Mol Cell Biochem       Date:  1982-05-28       Impact factor: 3.396

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