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Burst-by-Burst Measurement of Rotational Diffusion at Nanosecond Resolution Reveals Hot-Brownian Motion and Single-Chain Binding

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Baaske,  Martin Dieter       
Huygens-Kamerlingh Onnes Laboratory, Leiden University, Postbus, RA Leiden, The Netherlands;
Research Group Structure and Dynamics of Chromosomes, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Asgari, N., Baaske, M. D., & Orrit, M. (2023). Burst-by-Burst Measurement of Rotational Diffusion at Nanosecond Resolution Reveals Hot-Brownian Motion and Single-Chain Binding. ACS Nano, 17(13), 12684-12692. doi:10.1021/acsnano.3c03392.


Cite as: https://hdl.handle.net/21.11116/0000-000D-573F-C
Abstract
We record dark-field scattering bursts of individual gold nanorods, 52 × 15 nm2 in average size, freely diffusing in water suspension. We deduce their Brownian rotational diffusion constant from autocorrelation functions on a single-event basis. Due to spectral selection by the plasmonic resonance with the excitation laser, the distribution of rotational diffusion constants is much narrower than expected from the size distribution measured by TEM. As rotational diffusion depends on particle hydrodynamic volume, viscosity, and temperature, it can sense those parameters at the single-particle level. We demonstrate measurements of hot Brownian rotational diffusion of nanorods in temperature and viscosity gradients caused by plasmonic heating. Further, we monitor hydrodynamic volumes of gold nanorods upon addition of very low concentrations of the water-soluble polymer PVA, which binds to the particles, leading to measurable changes in their diffusion constant corresponding to binding of one to a few polymer coils. We propose this analysis technique for very low concentrations of biomolecules in solution.