Unknown

Dataset Information

0

Lateral association and elongation of vimentin intermediate filament proteins: A time-resolved light-scattering study.


ABSTRACT: Vimentin intermediate filaments (IFs) are part of a family of proteins that constitute one of the three filament systems in the cytoskeleton, a major contributor to cell mechanics. One property that distinguishes IFs from the other cytoskeletal filament types, actin filaments and microtubules, is their highly hierarchical assembly pathway, where a lateral association step is followed by elongation. Here we present an innovative technique to follow the elongation reaction in solution and in situ by time-resolved static and dynamic light scattering, thereby precisely capturing the relevant time and length scales of seconds to minutes and 60-600 nm, respectively. We apply a quantitative model to our data and succeed in consistently describing the entire set of data, including particle mass, radius of gyration, and hydrodynamic radius during longitudinal association.

SUBMITTER: Lopez CG 

PROVIDER: S-EPMC5056051 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Lateral association and elongation of vimentin intermediate filament proteins: A time-resolved light-scattering study.

Lopez Carlos G CG   Saldanha Oliva O   Huber Klaus K   Köster Sarah S  

Proceedings of the National Academy of Sciences of the United States of America 20160921 40


Vimentin intermediate filaments (IFs) are part of a family of proteins that constitute one of the three filament systems in the cytoskeleton, a major contributor to cell mechanics. One property that distinguishes IFs from the other cytoskeletal filament types, actin filaments and microtubules, is their highly hierarchical assembly pathway, where a lateral association step is followed by elongation. Here we present an innovative technique to follow the elongation reaction in solution and in situ  ...[more]

Similar Datasets

| S-EPMC8271578 | biostudies-literature
| S-EPMC4225453 | biostudies-literature
| S-EPMC2939553 | biostudies-literature
| S-EPMC6483650 | biostudies-literature
| S-EPMC7606667 | biostudies-literature
| S-EPMC3244446 | biostudies-literature
| S-EPMC6353089 | biostudies-literature
| S-EPMC9181571 | biostudies-literature
| S-EPMC6590062 | biostudies-literature
| S-EPMC4282252 | biostudies-literature