Bio-inspired active sheets: control of membrane shape dynamics by force-generating biopolymer networks
Lead Research Organisation:
University of Warwick
Department Name: Warwick Medical School
Abstract
The overall aim of this project is to develop an experimental system and a theoretical framework of bio-inspired active sheets that undergo controlled shape changes based on self-organisation of force generating biopolymers. The composite nature of the surface of mammalian cells, basically a lipid bilayer linked to an active actomyosin network, constitutes an exquisite example of an active sheet, that is robust and can take various geometries. Despite many research efforts, the underlying physical mechanisms by which actomyosin dynamics generate defined membrane shapes remain poorly understood. This problem combines hydrodynamics of the fluid lipid membrane with the mechanics of active polymer networks where effects on multiple length scales play a role.
Using a bottom-up approach we decorate giant unilamellar vesicles (GUVs) with thin networks of actin filaments and myosin motors and study how network activity and reorganisation drives membrane shape deformations at different length scales. By combining this with cutting edge 3D lattice light sheet microscopy (LLSM), quantitative image analysis and theory we want to test our hypothesis that the composition of thin, force generating actomyosin gels determines how lipid membranes adopt specific morphologies (tubes, ellipsoid, dumbbell). In addition, we plan to study the role of asymmetrical myosin distribution on GUV deformations by using micropipette assisted protein deposition. Using micropipette aspiration, we will address the role of membrane tension on shape changes in actomyosin decorated GUVs. Throughout the project, we will develop and test a theoretical model of such bio-inspired active sheets. The close back and forth communication between experimental and theoretical work will ensure an efficient planning of experiments and will accelerate the project overall.
A better theoretical and experimental grasp of the actomyosin-lipid membrane composite will be of high interest in the fields of biophysics, soft condensed matter, and engineering. This project will inform the design of active, controllable, and biocompatible carriers, will uncover basic principles governing cell shape control and will strengthen the capabilities of the UK science community in reconstituted, cell-like systems.
Using a bottom-up approach we decorate giant unilamellar vesicles (GUVs) with thin networks of actin filaments and myosin motors and study how network activity and reorganisation drives membrane shape deformations at different length scales. By combining this with cutting edge 3D lattice light sheet microscopy (LLSM), quantitative image analysis and theory we want to test our hypothesis that the composition of thin, force generating actomyosin gels determines how lipid membranes adopt specific morphologies (tubes, ellipsoid, dumbbell). In addition, we plan to study the role of asymmetrical myosin distribution on GUV deformations by using micropipette assisted protein deposition. Using micropipette aspiration, we will address the role of membrane tension on shape changes in actomyosin decorated GUVs. Throughout the project, we will develop and test a theoretical model of such bio-inspired active sheets. The close back and forth communication between experimental and theoretical work will ensure an efficient planning of experiments and will accelerate the project overall.
A better theoretical and experimental grasp of the actomyosin-lipid membrane composite will be of high interest in the fields of biophysics, soft condensed matter, and engineering. This project will inform the design of active, controllable, and biocompatible carriers, will uncover basic principles governing cell shape control and will strengthen the capabilities of the UK science community in reconstituted, cell-like systems.
People |
ORCID iD |
Darius Koester (Principal Investigator) |
Title | Balance |
Description | Together with Keneish dance, we have created a dance performance describing and playing with the rich membrane dynamics observed in neutrophils migrating through the extracellular matrix or squeezing through epithelial cell layers. |
Type Of Art | Performance (Music, Dance, Drama, etc) |
Year Produced | 2023 |
Impact | We have obtained additional funding from the Warwick Institute of Engagement to create the performance and display it at the Resonate festival 2023. The reaction of the public was positive and we have also visited a few schools to use the performance to talk about science and the scientific process to study cell membrane dynamics. Keneish dance has obtained further support to continue developing the ideas based on our initial exchanges and the collaboration is ongoing. |
URL | https://www.resonatefestival.co.uk/keneish-dance |
Description | Probing the mechano-biology of cell-cell adhesion in a novel single cell assay |
Amount | £165,353 (GBP) |
Funding ID | EP/Y002245/1 |
Organisation | Engineering and Physical Sciences Research Council (EPSRC) |
Sector | Public |
Country | United Kingdom |
Start | 12/2023 |
End | 11/2025 |
Description | Formation of lipid membrane vesicles containing actin and curly using eDice |
Organisation | Delft University of Technology (TU Delft) |
Country | Netherlands |
Sector | Academic/University |
PI Contribution | My lab provided the protein construct called curly. A member of my research team visited the laboratory of Prof. G. Koenderink to incorporate curly together with actin into giant unilamellar vesicles using their eDice technique and imaged them using fluorescence confocal microscopy. My lab is doing the quantitative image analysis. |
Collaborator Contribution | The Koenderink lab has provided their lab space and expertise to train my lab member in the eDice technology and have allowed us to use their fluorescence confocal microscope. |
Impact | The collaboration is ongoing and no output has been produced yet. |
Start Year | 2023 |