Literature DB >> 31539262

Minireview - Microtubules and Tubulin Oligomers: Shape Transitions and Assembly by Intrinsically Disordered Protein Tau and Cationic Biomolecules.

Cyrus R Safinya1, Peter J Chung2, Chaeyeon Song3, Youli Li4, Herbert P Miller5, Myung Chul Choi6, Uri Raviv7, Kai K Ewert1, Leslie Wilson5, Stuart C Feinstein5.   

Abstract

In this minireview, which is part of a special issue in honor of Jacob N. Israelachvili's remarkable research career on intermolecular forces and interfacial science, we present studies of structures, phase behavior, and forces in reaction mixtures of microtubules (MTs) and tubulin oligomers with either intrinsically disordered protein (IDP) Tau, cationic vesicles, or the polyamine spermine (4+). Bare MTs consist of 13 protofilaments (PFs), on average, where each PF is made of a linear stack of αβ-tubulin dimers (i.e., tubulin oligomers). We begin with a series of experiments which demonstrate the flexibility of PFs toward shape changes in response to local environmental cues. First, studies show that MT-associated protein (MAP) Tau controls the diameter of microtubules upon binding to the outer surface, implying a shape change in the cross-sectional area of PFs forming the MT perimeter. The diameter of a MT may also be controlled by the charge density of a lipid bilayer membrane that coats the outer surface. We further describe an experimental study where it is unexpectedly found that the biologically relevant polyamine spermine (+4e) is able to depolymerize taxol-stabilized microtubules with efficiency that increases with decreasing temperature. This MT destabilization drives a dynamical structural transition where inside-out curving of PFs, during the depolymerization peeling process, is followed by reassembly of ring-like curved PF building blocks into an array of helical inverted tubulin tubules. We finally turn to a very recent study on pressure-distance measurements in bundles of MTs employing the small-angle X-ray scattering (SAXS)-osmotic pressure technique, which complements the surface-forces-apparatus technique developed by Jacob N. Israelachvili. These latter studies are among the very few which are beginning to shed light on the precise nature of the interactions between MTs mediated by MAP Tau in 37 °C reaction mixtures containing GTP and lacking taxol.

Entities:  

Year:  2019        PMID: 31539262      PMCID: PMC6988848          DOI: 10.1021/acs.langmuir.9b02208

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  45 in total

Review 1.  Intrinsically unstructured proteins.

Authors:  Peter Tompa
Journal:  Trends Biochem Sci       Date:  2002-10       Impact factor: 13.807

Review 2.  Microtubules as a target for anticancer drugs.

Authors:  Mary Ann Jordan; Leslie Wilson
Journal:  Nat Rev Cancer       Date:  2004-04       Impact factor: 60.716

3.  Microtubule-associated protein tau (tau) is a major antigenic component of paired helical filaments in Alzheimer disease.

Authors:  K S Kosik; C L Joachim; D J Selkoe
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

4.  Interplay between liquid crystalline and isotropic gels in self-assembled neurofilament networks.

Authors:  Jayna B Jones; Cyrus R Safinya
Journal:  Biophys J       Date:  2008-07       Impact factor: 4.033

5.  Human microtubule-associated-protein tau regulates the number of protofilaments in microtubules: a synchrotron x-ray scattering study.

Authors:  M C Choi; U Raviv; H P Miller; M R Gaylord; E Kiris; D Ventimiglia; D J Needleman; M W Kim; L Wilson; S C Feinstein; C R Safinya
Journal:  Biophys J       Date:  2009-07-22       Impact factor: 4.033

6.  MAP2 is a component of crossbridges between microtubules and neurofilaments in the neuronal cytoskeleton: quick-freeze, deep-etch immunoelectron microscopy and reconstitution studies.

Authors:  N Hirokawa; S Hisanaga; Y Shiomura
Journal:  J Neurosci       Date:  1988-08       Impact factor: 6.167

Review 7.  The MAP2/Tau family of microtubule-associated proteins.

Authors:  Leif Dehmelt; Shelley Halpain
Journal:  Genome Biol       Date:  2004-12-23       Impact factor: 13.583

8.  MAP2 is required for dendrite elongation, PKA anchoring in dendrites, and proper PKA signal transduction.

Authors:  Akihiro Harada; Junlin Teng; Yosuke Takei; Keiko Oguchi; Nobutaka Hirokawa
Journal:  J Cell Biol       Date:  2002-08-05       Impact factor: 10.539

9.  Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

Authors:  B L Goode; S C Feinstein
Journal:  J Cell Biol       Date:  1994-03       Impact factor: 10.539

10.  Selective stabilization of tau in axons and microtubule-associated protein 2C in cell bodies and dendrites contributes to polarized localization of cytoskeletal proteins in mature neurons.

Authors:  N Hirokawa; T Funakoshi; R Sato-Harada; Y Kanai
Journal:  J Cell Biol       Date:  1996-02       Impact factor: 10.539

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