Semantic Scholar Open Access 2023 215 sitasi

Ångström-resolution fluorescence microscopy

Susanne C. M. Reinhardt Luciano A. Masullo I. Baudrexel Philipp R. Steen Rafal Kowalewski +7 lainnya

Abstrak

The authors introduce a single-molecule DNA-barcoding method, resolution enhancement by sequential imaging, that improves the resolution of fluorescence microscopy down to the Ångström scale using off-the-shelf fluorescence microscopy hardware and reagents. Fluorescence microscopy, with its molecular specificity, is one of the major characterization methods used in the life sciences to understand complex biological systems. Super-resolution approaches^ 1 – 6 can achieve resolution in cells in the range of 15 to 20 nm, but interactions between individual biomolecules occur at length scales below 10 nm and characterization of intramolecular structure requires Ångström resolution. State-of-the-art super-resolution implementations^ 7 – 14 have demonstrated spatial resolutions down to 5 nm and localization precisions of 1 nm under certain in vitro conditions. However, such resolutions do not directly translate to experiments in cells, and Ångström resolution has not been demonstrated to date. Here we introdue a DNA-barcoding method, resolution enhancement by sequential imaging (RESI), that improves the resolution of fluorescence microscopy down to the Ångström scale using off-the-shelf fluorescence microscopy hardware and reagents. By sequentially imaging sparse target subsets at moderate spatial resolutions of >15 nm, we demonstrate that single-protein resolution can be achieved for biomolecules in whole intact cells. Furthermore, we experimentally resolve the DNA backbone distance of single bases in DNA origami with Ångström resolution. We use our method in a proof-of-principle demonstration to map the molecular arrangement of the immunotherapy target CD20 in situ in untreated and drug-treated cells, which opens possibilities for assessing the molecular mechanisms of targeted immunotherapy. These observations demonstrate that, by enabling intramolecular imaging under ambient conditions in whole intact cells, RESI closes the gap between super-resolution microscopy and structural biology studies and thus delivers information key to understanding complex biological systems.

Topik & Kata Kunci

Penulis (12)

S

Susanne C. M. Reinhardt

L

Luciano A. Masullo

I

I. Baudrexel

P

Philipp R. Steen

R

Rafal Kowalewski

A

Alexandra S. Eklund

S

Sebastian Strauss

E

Eduard M. Unterauer

T

Thomas Schlichthaerle

M

Maximilian T. Strauss

C

Christian Klein

R

R. Jungmann

Format Sitasi

Reinhardt, S.C.M., Masullo, L.A., Baudrexel, I., Steen, P.R., Kowalewski, R., Eklund, A.S. et al. (2023). Ångström-resolution fluorescence microscopy. https://doi.org/10.1038/s41586-023-05925-9

Akses Cepat

Lihat di Sumber doi.org/10.1038/s41586-023-05925-9
Informasi Jurnal
Tahun Terbit
2023
Bahasa
en
Total Sitasi
215×
Sumber Database
Semantic Scholar
DOI
10.1038/s41586-023-05925-9
Akses
Open Access ✓