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Controlling pinned and coupled actomyosin contraction

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Abstract 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”). This differs from current experimental approaches that produce tangential contractile forces, as transverse anchoring enables axial force generation and loading as the actomyosin gel pulls the boundaries perpendicularly. 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 organisms.
Title: Controlling pinned and coupled actomyosin contraction
Description:
Abstract 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”).
This differs from current experimental approaches that produce tangential contractile forces, as transverse anchoring enables axial force generation and loading as the actomyosin gel pulls the boundaries perpendicularly.
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 organisms.

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