Cargando…
Twist response of actin filaments
Actin cytoskeleton force generation, sensing, and adaptation are dictated by the bending and twisting mechanics of filaments. Here, we use magnetic tweezers and microfluidics to twist and pull individual actin filaments and evaluate their response to applied loads. Twisted filaments bend and dissipa...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942836/ https://www.ncbi.nlm.nih.gov/pubmed/36656858 http://dx.doi.org/10.1073/pnas.2208536120 |
_version_ | 1784891584019431424 |
---|---|
author | Bibeau, Jeffrey P. Pandit, Nandan G. Gray, Shawn Shatery Nejad, Nooshin Sindelar, Charles V. Cao, Wenxiang De La Cruz, Enrique M. |
author_facet | Bibeau, Jeffrey P. Pandit, Nandan G. Gray, Shawn Shatery Nejad, Nooshin Sindelar, Charles V. Cao, Wenxiang De La Cruz, Enrique M. |
author_sort | Bibeau, Jeffrey P. |
collection | PubMed |
description | Actin cytoskeleton force generation, sensing, and adaptation are dictated by the bending and twisting mechanics of filaments. Here, we use magnetic tweezers and microfluidics to twist and pull individual actin filaments and evaluate their response to applied loads. Twisted filaments bend and dissipate torsional strain by adopting a supercoiled plectoneme. Pulling prevents plectoneme formation, which causes twisted filaments to sever. Analysis over a range of twisting and pulling forces and direct visualization of filament and single subunit twisting fluctuations yield an actin filament torsional persistence length of ~10 µm, similar to the bending persistence length. Filament severing by cofilin is driven by local twist strain at boundaries between bare and decorated segments and is accelerated by low pN pulling forces. This work explains how contractile forces generated by myosin motors accelerate filament severing by cofilin and establishes a role for filament twisting in the regulation of actin filament stability and assembly dynamics. |
format | Online Article Text |
id | pubmed-9942836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99428362023-07-19 Twist response of actin filaments Bibeau, Jeffrey P. Pandit, Nandan G. Gray, Shawn Shatery Nejad, Nooshin Sindelar, Charles V. Cao, Wenxiang De La Cruz, Enrique M. Proc Natl Acad Sci U S A Biological Sciences Actin cytoskeleton force generation, sensing, and adaptation are dictated by the bending and twisting mechanics of filaments. Here, we use magnetic tweezers and microfluidics to twist and pull individual actin filaments and evaluate their response to applied loads. Twisted filaments bend and dissipate torsional strain by adopting a supercoiled plectoneme. Pulling prevents plectoneme formation, which causes twisted filaments to sever. Analysis over a range of twisting and pulling forces and direct visualization of filament and single subunit twisting fluctuations yield an actin filament torsional persistence length of ~10 µm, similar to the bending persistence length. Filament severing by cofilin is driven by local twist strain at boundaries between bare and decorated segments and is accelerated by low pN pulling forces. This work explains how contractile forces generated by myosin motors accelerate filament severing by cofilin and establishes a role for filament twisting in the regulation of actin filament stability and assembly dynamics. National Academy of Sciences 2023-01-19 2023-01-24 /pmc/articles/PMC9942836/ /pubmed/36656858 http://dx.doi.org/10.1073/pnas.2208536120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Bibeau, Jeffrey P. Pandit, Nandan G. Gray, Shawn Shatery Nejad, Nooshin Sindelar, Charles V. Cao, Wenxiang De La Cruz, Enrique M. Twist response of actin filaments |
title | Twist response of actin filaments |
title_full | Twist response of actin filaments |
title_fullStr | Twist response of actin filaments |
title_full_unstemmed | Twist response of actin filaments |
title_short | Twist response of actin filaments |
title_sort | twist response of actin filaments |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942836/ https://www.ncbi.nlm.nih.gov/pubmed/36656858 http://dx.doi.org/10.1073/pnas.2208536120 |
work_keys_str_mv | AT bibeaujeffreyp twistresponseofactinfilaments AT panditnandang twistresponseofactinfilaments AT grayshawn twistresponseofactinfilaments AT shaterynejadnooshin twistresponseofactinfilaments AT sindelarcharlesv twistresponseofactinfilaments AT caowenxiang twistresponseofactinfilaments AT delacruzenriquem twistresponseofactinfilaments |