Hana Šípová-Jungová – Soft Matter Lab

Label-free nanofluidic scattering microscopy of size and mass of single diffusing molecules and nanoparticles published in Nature Methods

Kymographs of DNA inside Channel II. *(Image by the Authors.)*

Label-free nanofluidic scattering microscopy of size and mass of single diffusing molecules and nanoparticles
Barbora Špačková, Henrik Klein Moberg, Joachim Fritzsche, Johan Tenghamn, Gustaf Sjösten, Hana Šípová-Jungová, David Albinsson, Quentin Lubart, Daniel van Leeuwen, Fredrik Westerlund, Daniel Midtvedt, Elin K. Esbjörner, Mikael Käll, Giovanni Volpe & Christoph Langhammer
Nature Methods 19, 751–758 (2022)
doi: 10.1038/s41592-022-01491-6

Label-free characterization of single biomolecules aims to complement fluorescence microscopy in situations where labeling compromises data interpretation, is technically challenging or even impossible. However, existing methods require the investigated species to bind to a surface to be visible, thereby leaving a large fraction of analytes undetected. Here, we present nanofluidic scattering microscopy (NSM), which overcomes these limitations by enabling label-free, real-time imaging of single biomolecules diffusing inside a nanofluidic channel. NSM facilitates accurate determination of molecular weight from the measured optical contrast and of the hydrodynamic radius from the measured diffusivity, from which information about the conformational state can be inferred. Furthermore, we demonstrate its applicability to the analysis of a complex biofluid, using conditioned cell culture medium containing extracellular vesicles as an example. We foresee the application of NSM to monitor conformational changes, aggregation and interactions of single biomolecules, and to analyze single-cell secretomes.

Presentation by F. Schmidt at OSA-OMA-2021

Non-spherical nanoparticle held by optical tweezers. The particle is trapped against the cover slide.

Dynamics of an Active Nanoparticle in an Optical Trap
Falko Schmidt, Hana Sipova-Jungova, Mikael Käll, Alois Würger, Giovanni Volpe
Submitted as OSA-OMA-2021, AF1D.2 Contribution
Date: 16 April
Time: 12:30 CEST

Short Abstract
We investigate a nanoparticle inside an optical trap and driven away from equilibrium by self-induced concentration gradients. We find that a nanoparticle performs fast orbital rotations and its probability density shifting away from equilibrium.

Non-equilibrium properties of an active nanoparticle in a harmonic potential published in Nature Commun.

Non-equilibrium properties of an active nanoparticle in a harmonic potential
Falko Schmidt, Hana Šípová-Jungová, Mikael Käll, Alois Würger & Giovanni Volpe
Nature Communications 12, 1902 (2021)
doi: 10.1038/s41467-021-22187-z
arXiv: 2009.08393

Active particles break out of thermodynamic equilibrium thanks to their directed motion, which leads to complex and interesting behaviors in the presence of confining potentials. When dealing with active nanoparticles, however, the overwhelming presence of rotational diffusion hinders directed motion, leading to an increase of their effective temperature, but otherwise masking the effects of self-propulsion. Here, we demonstrate an experimental system where an active nanoparticle immersed in a critical solution and held in an optical harmonic potential features far-from-equilibrium behavior beyond an increase of its effective temperature. When increasing the laser power, we observe a cross-over from a Boltzmann distribution to a non-equilibrium state, where the particle performs fast orbital rotations about the beam axis. These findings are rationalized by solving the Fokker-Planck equation for the particle’s position and orientation in terms of a moment expansion. The proposed self-propulsion mechanism results from the particle’s non-sphericity and the lower critical point of the solute.