Label-free nanofluidic scattering microscopy of size and mass of single diffusing molecules and nanoparticles

被引:40
|
作者
Spackova, Barbora [1 ]
Moberg, Henrik Klein [1 ]
Fritzsche, Joachim [1 ]
Tenghamn, Johan [1 ]
Sjosten, Gustaf [2 ]
Sipova-Jungova, Hana [1 ]
Albinsson, David [1 ]
Lubart, Quentin [3 ]
van Leeuwen, Daniel [3 ]
Westerlund, Fredrik [3 ]
Midtvedt, Daniel [2 ]
Esbjorner, Elin K. [3 ]
Kall, Mikael [1 ]
Volpe, Giovanni [2 ]
Langhammer, Christoph [1 ]
机构
[1] Chalmers Univ Technol, Dept Phys, Gothenburg, Sweden
[2] Univ Gothenburg, Dept Phys, Gothenburg, Sweden
[3] Chalmers Univ Technol, Dept Biol & Biol Engn, Gothenburg, Sweden
关键词
TRACKING; PARTICLES; MEMBRANE;
D O I
10.1038/s41592-022-01491-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanofluidic scattering microscopy enables label-free, quantitative measurements of the molecular weight and hydrodynamic radius of biological molecules and nanoparticles freely diffusing inside a nanofluidic channel. 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.
引用
收藏
页码:751 / +
页数:17
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