scholarly journals Label-Free Super-Resolution Microscopy By Means of Transient Absorption Saturation

2021 ◽  
Vol 120 (3) ◽  
pp. 181a
Author(s):  
Behjat Sadat Kariman ◽  
Takahiro Deguchi ◽  
Marco Scotto d'Abbusco ◽  
Giulia Zanini ◽  
Alberto Diaspro ◽  
...  
2021 ◽  
Author(s):  
xue cheng ◽  
Congyue Liu ◽  
Guorui Zhang ◽  
Wei Liu ◽  
Ju wang ◽  
...  

2018 ◽  
Vol 27 (11) ◽  
pp. 118704 ◽  
Author(s):  
Xiaowei Liu ◽  
Chao Meng ◽  
Xuechu Xu ◽  
Mingwei Tang ◽  
Chenlei Pang ◽  
...  

ACS Photonics ◽  
2015 ◽  
Vol 3 (1) ◽  
pp. 79-86 ◽  
Author(s):  
W. Ruchira Silva ◽  
Christian T. Graefe ◽  
Renee R. Frontiera

Small Methods ◽  
2021 ◽  
pp. 2000985
Author(s):  
Milan Vala ◽  
Łukasz Bujak ◽  
Antonio García Marín ◽  
Kristýna Holanová ◽  
Verena Henrichs ◽  
...  

Small Methods ◽  
2021 ◽  
Vol 5 (4) ◽  
pp. 2170012
Author(s):  
Milan Vala ◽  
Łukasz Bujak ◽  
Antonio García Marín ◽  
Kristýna Holanová ◽  
Verena Henrichs ◽  
...  

2021 ◽  
Vol 1 ◽  
pp. 3
Author(s):  
Alberto Aguilar ◽  
Adeline Boyreau ◽  
Pierre Bon

Background: Achieving resolutions below 100 nm is key for many fields, including biology and nanomaterial characterization. Although nearfield and electron microscopy are the gold standards for studying the nanoscale, optical microscopy has seen its resolution drastically improve in the last decades. So-called super-resolution microscopy is generally based on fluorescence photophysics and requires modification of the sample at least by adding fluorescent tags, an inevitably invasive step. Therefore, it remains very challenging and rewarding to achieve optical resolutions beyond the diffraction limit in label-free samples. Methods: Here, we present a breakthrough to unlock label-free 3D super-resolution imaging of any object including living biological samples. It is based on optical photon-reassignment in confocal reflectance imaging mode. Results: We demonstrate that we surpass the resolution of all fluorescence-based confocal systems by a factor ~1.5. We have obtained images with a 3D (x,y,z) optical resolution of (86x86x248) nm3 using a visible wavelength (445 nm) and a regular microscope objective (NA=1.3). The results are presented on nanoparticles as well as on (living) biological samples. Conclusions: This cost-effective approach double the resolution of reflectance confocal microscope with minimal modifications. It is therefore compatible with any microscope and sample, works in real-time, and does not require any signal processing.


2020 ◽  
Author(s):  
Milan Vala ◽  
Łukasz Bujak ◽  
Antonio García Marín ◽  
Kristýna Holanová ◽  
Verena Henrichs ◽  
...  

AbstractMicrotubules are cytoskeletal polymers of tubulin dimers assembled into protofilaments that constitute nanotubes undergoing periods of assembly and disassembly. Static electron micrographs suggest a structural transition of straight protofilaments into curved ones occurring at the tips of disassembling microtubules. However, these structural transitions have never been observed and the process of microtubule disassembly thus remains unclear. Here, a label-free optical microscopy capable of selective imaging of the transient structural changes of protofilaments at the tip of a disassembling microtubule is introduced. Upon induced disassembly, the transition of ordered protofilaments into a disordered conformation is resolved at the tip of the microtubule. Imaging the unbinding of individual tubulin oligomers from the microtubule tip reveals transient pauses and relapses in the disassembly, concurrent with enrichment of ordered protofilament segments at the microtubule tip. These findings show that microtubule disassembly is a discrete process and suggest a mechanism of switching from the disassembly to the assembly phase.


2021 ◽  
Vol 120 (3) ◽  
pp. 181a
Author(s):  
Milan Vala ◽  
Łukasz Bujak ◽  
Antonio G. Marin ◽  
Kristýna Holanová ◽  
Verena Henrichs ◽  
...  

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