Published January 2, 2024 | Version v1
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Highly flexible PEG-LifeAct constructs act as tunable biomimetic actin crosslinkers

Description

In vitro studies of actin filament networks crosslinked with dynamic actin binding proteins provide critical insights into cytoskeletal mechanics as well as inspiration for new adaptive materials design. However, discontinuous variance in the physiochemical properties of actin binding proteins impedes holistic relationships between crosslinker molecular parameters, network structure, and mechanics. Bio-synthetic constructs composed of synthetic polymer backbones and actin binding motifs would enable crosslinkers with engineered physiochemical properties to directly target the desired structure–property relationships. As a proof of concept, bio-synthetic crosslinkers composed of highly flexible polyethylene glycol (PEG) polymers functionalized with the actin binding peptide LifeAct, are explored as actin crosslinkers. Using bulk rheology and fluorescence microscopy, these constructs are shown to modulate actin filament network structure and mechanics in a contour length dependent manner, while maintaining the stress-stiffening behavior inherent to actin filament networks. These results encourage the design of more diverse and complex peptide-polymer crosslinkers to interrogate and control semi-flexible polymer networks.

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Additional details

Identifiers

DOI
10.1039/D3SM01341C
Other
oai:uchicago.tind.io:11447

Funding

National Science Foundation
DMR-2011854
National Science Foundation
DMR-2215605
National Institutes of Health
R01 GM079265

UChicago Information

Division(s)
Biological Sciences Division, Physical Sciences Division, Pritzker School of Molecular Engineering
Department(s)
Biochemistry and Molecular Biology, Chemistry, Molecular Genetics and Cell Biology, Physics
Center(s) or Institute(s)
Institute for Biophysical Dynamics, James Franck Institute