Experimental methods to control pinned and coupled actomyosin contraction events

Fuente: arXiv
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Autores principales: Clarke, James, Lee, Hyunjae, Wong, Kyla, Glenn, Julia, Marne, Aniket, Miyahara, Yoichi, Alvarado, José
Formato: Preprint
Publicado: 2025
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author Clarke, James
Lee, Hyunjae
Wong, Kyla
Glenn, Julia
Marne, Aniket
Miyahara, Yoichi
Alvarado, José
author_facet Clarke, James
Lee, Hyunjae
Wong, Kyla
Glenn, Julia
Marne, Aniket
Miyahara, Yoichi
Alvarado, José
contents Actin and myosin drive many instances of force generation, deformation, and shape change in cells, tissues, and organisms. In particular, cytoskeletal actomyosin is remarkable in its adaptive architecture, responding to a host of actin-binding proteins. Equally important, however, is actomyosin's interaction with its mechanical environment. Actomyosin contractility and environmental properties, such as geometry and stiffness, are inherently coupled. To understand this coupling, novel experimental techniques are needed. Here we describe methods to spatially control the anchoring of reconstituted contractile actomyosin networks to two, opposing surfaces ("transverse anchoring"). The two surfaces can be either rigid ("pinned contraction"), or one of the surfaces may be compliant ("coupled contraction"). We introduce compliance by manufacturing flexure hinges, and describe their calibration. Calibration permits a direct measurement of the contractile force and mechanical work that actomyosin exerts on the environment. The methods described here provide an avenue toward a more complete characterization of actomyosin's role as an actuator, an essential property in its context of driving deformation and shape change in living systems.
format Preprint
id arxiv_https___arxiv_org_abs_2512_15602
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Experimental methods to control pinned and coupled actomyosin contraction events
Clarke, James
Lee, Hyunjae
Wong, Kyla
Glenn, Julia
Marne, Aniket
Miyahara, Yoichi
Alvarado, José
Soft Condensed Matter
Actin and myosin drive many instances of force generation, deformation, and shape change in cells, tissues, and organisms. In particular, cytoskeletal actomyosin is remarkable in its adaptive architecture, responding to a host of actin-binding proteins. Equally important, however, is actomyosin's interaction with its mechanical environment. Actomyosin contractility and environmental properties, such as geometry and stiffness, are inherently coupled. To understand this coupling, novel experimental techniques are needed. Here we describe methods to spatially control the anchoring of reconstituted contractile actomyosin networks to two, opposing surfaces ("transverse anchoring"). The two surfaces can be either rigid ("pinned contraction"), or one of the surfaces may be compliant ("coupled contraction"). We introduce compliance by manufacturing flexure hinges, and describe their calibration. Calibration permits a direct measurement of the contractile force and mechanical work that actomyosin exerts on the environment. The methods described here provide an avenue toward a more complete characterization of actomyosin's role as an actuator, an essential property in its context of driving deformation and shape change in living systems.
title Experimental methods to control pinned and coupled actomyosin contraction events
topic Soft Condensed Matter
url https://arxiv.org/abs/2512.15602