Real-time dynamics of emerging actin networks in cell-mimicking compartments.

Understanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in c...

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Main Authors: Siddharth Deshpande, Thomas Pfohl
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4364982?pdf=render
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spelling doaj-ec3007a106d24770a306f4f06cf344362020-11-25T01:58:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e011652110.1371/journal.pone.0116521Real-time dynamics of emerging actin networks in cell-mimicking compartments.Siddharth DeshpandeThomas PfohlUnderstanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in cell motility, environmental exploration, intracellular transport and mechanical stability. Though the viscoelastic properties of actin-based structures have been extensively probed, the underlying microstructure dynamics, especially their disassembly, is not fully understood. In this article, we explore the rich dynamics and emergent properties exhibited by actin bundles within flow-free confinements using a microfluidic set-up and epifluorescence microscopy. After forming entangled actin filaments within cell-sized quasi two-dimensional confinements, we induce their bundling using three different fundamental mechanisms: counterion condensation, depletion interactions and specific protein-protein interactions. Intriguingly, long actin filaments form emerging networks of actin bundles via percolation leading to remarkable properties such as stress generation and spindle-like intermediate structures. Simultaneous sharing of filaments in different links of the network is an important parameter, as short filaments do not form networks but segregated clusters of bundles instead. We encounter a hierarchical process of bundling and its subsequent disassembly. Additionally, our study suggests that such percolated networks are likely to exist within living cells in a dynamic fashion. These observations render a perspective about differential cytoskeletal responses towards numerous stimuli.http://europepmc.org/articles/PMC4364982?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Siddharth Deshpande
Thomas Pfohl
spellingShingle Siddharth Deshpande
Thomas Pfohl
Real-time dynamics of emerging actin networks in cell-mimicking compartments.
PLoS ONE
author_facet Siddharth Deshpande
Thomas Pfohl
author_sort Siddharth Deshpande
title Real-time dynamics of emerging actin networks in cell-mimicking compartments.
title_short Real-time dynamics of emerging actin networks in cell-mimicking compartments.
title_full Real-time dynamics of emerging actin networks in cell-mimicking compartments.
title_fullStr Real-time dynamics of emerging actin networks in cell-mimicking compartments.
title_full_unstemmed Real-time dynamics of emerging actin networks in cell-mimicking compartments.
title_sort real-time dynamics of emerging actin networks in cell-mimicking compartments.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Understanding the cytoskeletal functionality and its relation to other cellular components and properties is a prominent question in biophysics. The dynamics of actin cytoskeleton and its polymorphic nature are indispensable for the proper functioning of living cells. Actin bundles are involved in cell motility, environmental exploration, intracellular transport and mechanical stability. Though the viscoelastic properties of actin-based structures have been extensively probed, the underlying microstructure dynamics, especially their disassembly, is not fully understood. In this article, we explore the rich dynamics and emergent properties exhibited by actin bundles within flow-free confinements using a microfluidic set-up and epifluorescence microscopy. After forming entangled actin filaments within cell-sized quasi two-dimensional confinements, we induce their bundling using three different fundamental mechanisms: counterion condensation, depletion interactions and specific protein-protein interactions. Intriguingly, long actin filaments form emerging networks of actin bundles via percolation leading to remarkable properties such as stress generation and spindle-like intermediate structures. Simultaneous sharing of filaments in different links of the network is an important parameter, as short filaments do not form networks but segregated clusters of bundles instead. We encounter a hierarchical process of bundling and its subsequent disassembly. Additionally, our study suggests that such percolated networks are likely to exist within living cells in a dynamic fashion. These observations render a perspective about differential cytoskeletal responses towards numerous stimuli.
url http://europepmc.org/articles/PMC4364982?pdf=render
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