Literature DB >> 16582470

Elastic and damping forces generated by confined arrays of dynamic microtubules.

J Howard1.   

Abstract

In addition to serving as structural elements and as tracks for motor proteins, microtubules use chemical energy derived from the hydrolysis of GTP to generate forces when growing and shrinking. These forces are used to push or pull on organelles such as chromosomes and the mitotic spindle. If an array of microtubules grows out from a nucleation site and is confined by the periphery of the cell, pushing and pulling forces can give rise to interesting collective phenomena. In this paper, I show that pushing forces center the array provided that the microtubules are dynamic in the sense that they switch from pushing to shrinking after reaching the periphery. Microtubule dynamics of free ends is neither necessary nor sufficient for centering. Buckling can augment the centering force. For small displacements and velocities, the array can be modeled very simply as a damped spring. The dynamic stiffness of the array is orders of magnitude smaller than its static stiffness, and the relaxation time is on the order of the time that it takes for a microtubule to grow from the center to the periphery. Replacement of a dynamic polymer array with an equivalent mechanical circuit provides a bridge between molecular and cellular mechanics.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16582470     DOI: 10.1088/1478-3975/3/1/006

Source DB:  PubMed          Journal:  Phys Biol        ISSN: 1478-3967            Impact factor:   2.583


  37 in total

1.  Symmetry, stability, and reversibility properties of idealized confined microtubule cytoskeletons.

Authors:  V I Maly; I V Maly
Journal:  Biophys J       Date:  2010-11-03       Impact factor: 4.033

Review 2.  Towards a quantitative understanding of mitotic spindle assembly and mechanics.

Authors:  Alex Mogilner; Erin Craig
Journal:  J Cell Sci       Date:  2010-10-15       Impact factor: 5.285

3.  Contribution of whole-cell optimization via cell body rolling to polarization of T cells.

Authors:  Sergey N Arkhipov; Ivan V Maly
Journal:  Phys Biol       Date:  2006-10-03       Impact factor: 2.583

4.  Bundling, sliding, and pulling microtubules in cells and in silico.

Authors:  Jonathon Howard; Iva M Tolić-Nørrelykke
Journal:  HFSP J       Date:  2007-05-21

Review 5.  End-on microtubule-dynein interactions and pulling-based positioning of microtubule organizing centers.

Authors:  Liedewij Laan; Sophie Roth; Marileen Dogterom
Journal:  Cell Cycle       Date:  2012-08-16       Impact factor: 4.534

Review 6.  Growth, fluctuation and switching at microtubule plus ends.

Authors:  Jonathon Howard; Anthony A Hyman
Journal:  Nat Rev Mol Cell Biol       Date:  2009-06-10       Impact factor: 94.444

7.  Growth and shortening of microtubules: a two-state model approach.

Authors:  Yunxin Zhang
Journal:  J Biol Chem       Date:  2011-09-07       Impact factor: 5.157

8.  Buckling behavior of individual and bundled microtubules.

Authors:  Mohammad Soheilypour; Mohaddeseh Peyro; Stephen J Peter; Mohammad R K Mofrad
Journal:  Biophys J       Date:  2015-04-07       Impact factor: 4.033

9.  Characterization of microtubule buckling in living cells.

Authors:  Carla Pallavicini; Alejandro Monastra; Nicolás González Bardeci; Diana Wetzler; Valeria Levi; Luciana Bruno
Journal:  Eur Biophys J       Date:  2017-04-19       Impact factor: 1.733

10.  Self-organization of dynein motors generates meiotic nuclear oscillations.

Authors:  Sven K Vogel; Nenad Pavin; Nicola Maghelli; Frank Jülicher; Iva M Tolić-Nørrelykke
Journal:  PLoS Biol       Date:  2009-04-21       Impact factor: 8.029

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.