Literature DB >> 15819415

Characterization of the in vitro co-assembly process of the intermediate filament proteins vimentin and desmin: mixed polymers at all stages of assembly.

Ute Wickert1, Norbert Mücke, Tatjana Wedig, Shirley A Müller, Ueli Aebi, Harald Herrmann.   

Abstract

We have investigated the co-assembly properties of the intermediate filament (IF) proteins vimentin and desmin. First, the soluble complexes formed by both proteins separately in 5 mM Tris-HCl, pH 8.4, were characterized by analytical ultracentrifugation. In both cases, s-values of around 5 S were obtained corresponding to the formation of tetramers. However, at pH 7.5 and in the presence of 1 mM EDTA, both proteins behaved quite differently; whereas vimentin sedimented at 7.2 S, desmin assembled into much larger complexes of about 13 S. A mixture of equimolar amounts of vimentin and desmin in 8 M urea yielded, after reconstitution into 5 mM Tris-HCl, pH 7.5, and 1 mM EDTA, complexes exhibiting a sharp peak at 10.9 S. This intermediate s-value indicated that co-assembly into a distinct new set of complexes had occurred. As judged by electron microscopy and viscometry, these mixtures assembled into IFs with characteristics similar to those of pure vimentin and desmin. Furthermore, when vimentin and desmin tetramers were mixed in 5 mM Tris-HCl, pH 8.4, and subsequently subjected to IF assembly conditions, again "hybrid" filaments were obtained. Most interestingly, after 10 min of assembly, mass-per-length (MPL) measurements by scanning transmission electron microscopy yielded IFs with an MPL-peak value of 36 +/- 5 kDa/nm, hence closer to that of vimentin IFs (33 +/- 4 kDa/nm) than to that of desmin IFs (48 +/- 8 kDa/nm). Finally, when unit length-filaments (ULF) of vimentin and desmin were mixed and assembled further, the diameters of individual mature IFs formed exhibited a significantly higher degree of width inhomogeneity along their length than vimentin and desmin IFs as might be expected for a modular mode of assembly. Last but not least, atomic force microscopy provided further direct evidence that desmin IFs are able to fuse end-to-end with vimentin IFs. In summary, we have shown that vimentin and desmin are able to co-assemble at the dimer, tetramer, ULF and even the mature IF level.

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Year:  2005        PMID: 15819415     DOI: 10.1016/j.ejcb.2005.01.004

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  16 in total

Review 1.  Intermediate filaments in smooth muscle.

Authors:  Dale D Tang
Journal:  Am J Physiol Cell Physiol       Date:  2008-02-06       Impact factor: 4.249

2.  Severing and end-to-end annealing of neurofilaments in neurons.

Authors:  Atsuko Uchida; Gülsen Çolakoğlu; Lina Wang; Paula C Monsma; Anthony Brown
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-02       Impact factor: 11.205

3.  Disease mutations in the "head" domain of the extra-sarcomeric protein desmin distinctly alter its assembly and network-forming properties.

Authors:  Sarika Sharma; Norbert Mücke; Hugo A Katus; Harald Herrmann; Harald Bär
Journal:  J Mol Med (Berl)       Date:  2009-09-08       Impact factor: 4.599

4.  Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages.

Authors:  Harald Bär; Norbert Mücke; Anna Kostareva; Gunnar Sjöberg; Ueli Aebi; Harald Herrmann
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-10       Impact factor: 11.205

5.  Assembly Kinetics of Vimentin Tetramers to Unit-Length Filaments: A Stopped-Flow Study.

Authors:  Norbert Mücke; Lara Kämmerer; Stefan Winheim; Robert Kirmse; Jan Krieger; Maria Mildenberger; Jochen Baßler; Ed Hurt; Wolfgang H Goldmann; Ueli Aebi; Katalin Toth; Jörg Langowski; Harald Herrmann
Journal:  Biophys J       Date:  2018-05-10       Impact factor: 4.033

6.  A crystal structure of coil 1B of vimentin in the filamentous form provides a model of a high-order assembly of a vimentin filament.

Authors:  Allan H Pang; Josiah M Obiero; Arkadiusz W Kulczyk; Vitaliy M Sviripa; Oleg V Tsodikov
Journal:  FEBS J       Date:  2018-06-25       Impact factor: 5.542

7.  Filamentous biopolymers on surfaces: atomic force microscopy images compared with Brownian dynamics simulation of filament deposition.

Authors:  Norbert Mücke; Konstantin Klenin; Robert Kirmse; Malte Bussiek; Harald Herrmann; Mathias Hafner; Jörg Langowski
Journal:  PLoS One       Date:  2009-11-04       Impact factor: 3.240

8.  Dynamics of the bacterial intermediate filament crescentin in vitro and in vivo.

Authors:  Osigwe Esue; Laura Rupprecht; Sean X Sun; Denis Wirtz
Journal:  PLoS One       Date:  2010-01-25       Impact factor: 3.240

9.  Deconstructing the late phase of vimentin assembly by total internal reflection fluorescence microscopy (TIRFM).

Authors:  Stefan Winheim; Aaron R Hieb; Marleen Silbermann; Eva-Maria Surmann; Tatjana Wedig; Harald Herrmann; Jörg Langowski; Norbert Mücke
Journal:  PLoS One       Date:  2011-04-22       Impact factor: 3.240

10.  Intermediate filaments exchange subunits along their length and elongate by end-to-end annealing.

Authors:  Gülsen Colakoğlu; Anthony Brown
Journal:  J Cell Biol       Date:  2009-05-25       Impact factor: 10.539

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