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In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study
Intermediate filament (IF) elongation proceeds via full-width “mini-filaments”, referred to as “unit-length” filaments (ULFs), which instantaneously form by lateral association of extended coiled-coil complexes after assembly is initiated. In a comparatively much slower process, ULFs longitudinally...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909217/ https://www.ncbi.nlm.nih.gov/pubmed/27304995 http://dx.doi.org/10.1371/journal.pone.0157451 |
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author | Mücke, Norbert Winheim, Stefan Merlitz, Holger Buchholz, Jan Langowski, Jörg Herrmann, Harald |
author_facet | Mücke, Norbert Winheim, Stefan Merlitz, Holger Buchholz, Jan Langowski, Jörg Herrmann, Harald |
author_sort | Mücke, Norbert |
collection | PubMed |
description | Intermediate filament (IF) elongation proceeds via full-width “mini-filaments”, referred to as “unit-length” filaments (ULFs), which instantaneously form by lateral association of extended coiled-coil complexes after assembly is initiated. In a comparatively much slower process, ULFs longitudinally interact end-to-end with other ULFs to form short filaments, which further anneal with ULFs and with each other to increasingly longer filaments. This assembly concept was derived from time-lapse electron and atomic force microscopy data. We previously have quantitatively verified this concept through the generation of time-dependent filament length-profiles and an analytical model that describes assembly kinetics well for about the first ten minutes. In this time frame, filaments are shorter than one persistence length, i.e. ~1 μm, and thus filaments were treated as stiff rods associating via their ends. However, when filaments grow several μm in length over hours, their flexibility becomes a significant factor for the kinetics of the longitudinal annealing process. Incorporating now additional filament length distributions that we have recorded after extended assembly times by total internal reflection fluorescence microscopy (TIRFM), we developed a Monte Carlo simulation procedure that accurately describes the underlying assembly kinetics for large time scales. |
format | Online Article Text |
id | pubmed-4909217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49092172016-07-06 In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study Mücke, Norbert Winheim, Stefan Merlitz, Holger Buchholz, Jan Langowski, Jörg Herrmann, Harald PLoS One Research Article Intermediate filament (IF) elongation proceeds via full-width “mini-filaments”, referred to as “unit-length” filaments (ULFs), which instantaneously form by lateral association of extended coiled-coil complexes after assembly is initiated. In a comparatively much slower process, ULFs longitudinally interact end-to-end with other ULFs to form short filaments, which further anneal with ULFs and with each other to increasingly longer filaments. This assembly concept was derived from time-lapse electron and atomic force microscopy data. We previously have quantitatively verified this concept through the generation of time-dependent filament length-profiles and an analytical model that describes assembly kinetics well for about the first ten minutes. In this time frame, filaments are shorter than one persistence length, i.e. ~1 μm, and thus filaments were treated as stiff rods associating via their ends. However, when filaments grow several μm in length over hours, their flexibility becomes a significant factor for the kinetics of the longitudinal annealing process. Incorporating now additional filament length distributions that we have recorded after extended assembly times by total internal reflection fluorescence microscopy (TIRFM), we developed a Monte Carlo simulation procedure that accurately describes the underlying assembly kinetics for large time scales. Public Library of Science 2016-06-15 /pmc/articles/PMC4909217/ /pubmed/27304995 http://dx.doi.org/10.1371/journal.pone.0157451 Text en © 2016 Mücke et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mücke, Norbert Winheim, Stefan Merlitz, Holger Buchholz, Jan Langowski, Jörg Herrmann, Harald In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title | In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title_full | In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title_fullStr | In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title_full_unstemmed | In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title_short | In Vitro Assembly Kinetics of Cytoplasmic Intermediate Filaments: A Correlative Monte Carlo Simulation Study |
title_sort | in vitro assembly kinetics of cytoplasmic intermediate filaments: a correlative monte carlo simulation study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909217/ https://www.ncbi.nlm.nih.gov/pubmed/27304995 http://dx.doi.org/10.1371/journal.pone.0157451 |
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