Summary
At the core of far-from-equilibrium biological activity lies an orchestra of molecular motors, constantly dissipating energy while converting chemical fuel into mechanical work. Estimating the amount of the free energy budget lost to dissipation is crucial for a deeper understanding of the underlying nonequilibrium dynamics and for unravelling the thermodynamic constraints on the possible biological processes. Although there are theoretical tools for quantifying nonequilibrium activity and dissipation in the framework of stochastic thermodynamics, there is a gap between these analytical calculations and their experimental applicability. The difficulty stems from the limited accessibility to the myriad degrees of freedom of complex systems and the finite measurement resolution, which can mask the footprints of nonequilibrium dynamics, such that they may appear as passive thermal fluctuations.
I will address this challenge both experimentally and theoretically. In my lab, I will develop fluorescent nanosensors for unveiling microscopic activity otherwise inaccessible in complex biological systems. Fluorescent single-walled carbon nanotubes with tailored functionalization will transduce molecular-motor activity to a modulation of the emitted fluorescence, providing a novel degree of freedom never before exploited as a phase-space coordinate for inferring dissipation in nonequilibrium systems. I will incorporate the nanotube sensors in minimal biomimetic models of active systems, including DNA-gel and reconstituted cytoskeleton driven by molecular motors, to demonstrate my approach in a highly controlled environment. Further, I will internalize the nanotubes within live cells, and utilize the fluorescence signal to estimate the dissipation in nonequilibrium intracellular organization. In parallel, I will advance theoretical tools for estimating the dissipation from experimental data, based on an approach I have pioneered for detecting time-irreversibility.
I will address this challenge both experimentally and theoretically. In my lab, I will develop fluorescent nanosensors for unveiling microscopic activity otherwise inaccessible in complex biological systems. Fluorescent single-walled carbon nanotubes with tailored functionalization will transduce molecular-motor activity to a modulation of the emitted fluorescence, providing a novel degree of freedom never before exploited as a phase-space coordinate for inferring dissipation in nonequilibrium systems. I will incorporate the nanotube sensors in minimal biomimetic models of active systems, including DNA-gel and reconstituted cytoskeleton driven by molecular motors, to demonstrate my approach in a highly controlled environment. Further, I will internalize the nanotubes within live cells, and utilize the fluorescence signal to estimate the dissipation in nonequilibrium intracellular organization. In parallel, I will advance theoretical tools for estimating the dissipation from experimental data, based on an approach I have pioneered for detecting time-irreversibility.
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| Web resources: | https://cordis.europa.eu/project/id/101039127 |
| Start date: | 01-10-2022 |
| End date: | 30-09-2027 |
| Total budget - Public funding: | 1 500 000,00 Euro - 1 500 000,00 Euro |
Cordis data
Original description
At the core of far-from-equilibrium biological activity lies an orchestra of molecular motors, constantly dissipating energy while converting chemical fuel into mechanical work. Estimating the amount of the free energy budget lost to dissipation is crucial for a deeper understanding of the underlying nonequilibrium dynamics and for unravelling the thermodynamic constraints on the possible biological processes. Although there are theoretical tools for quantifying nonequilibrium activity and dissipation in the framework of stochastic thermodynamics, there is a gap between these analytical calculations and their experimental applicability. The difficulty stems from the limited accessibility to the myriad degrees of freedom of complex systems and the finite measurement resolution, which can mask the footprints of nonequilibrium dynamics, such that they may appear as passive thermal fluctuations.I will address this challenge both experimentally and theoretically. In my lab, I will develop fluorescent nanosensors for unveiling microscopic activity otherwise inaccessible in complex biological systems. Fluorescent single-walled carbon nanotubes with tailored functionalization will transduce molecular-motor activity to a modulation of the emitted fluorescence, providing a novel degree of freedom never before exploited as a phase-space coordinate for inferring dissipation in nonequilibrium systems. I will incorporate the nanotube sensors in minimal biomimetic models of active systems, including DNA-gel and reconstituted cytoskeleton driven by molecular motors, to demonstrate my approach in a highly controlled environment. Further, I will internalize the nanotubes within live cells, and utilize the fluorescence signal to estimate the dissipation in nonequilibrium intracellular organization. In parallel, I will advance theoretical tools for estimating the dissipation from experimental data, based on an approach I have pioneered for detecting time-irreversibility.
Status
SIGNEDCall topic
ERC-2021-STGUpdate Date
09-02-2023
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