Application of single-molecule switching nanoscopy (SMSN) beyond the coverslip surface poses substantial challenges due to sample-induced aberrations that distort and blur single-molecule emission patterns. We combined active shaping of point spread functions and efficient adaptive optics to enable robust 3D-SMSN imaging within tissues. This development allowed us to image through 30-$\mu$m-thick brain sections to visualize and reconstruct the morphology and the nanoscale details of amyloid-$\beta$ filaments in a mouse model of Alzheimer's disease.
%0 Journal Article
%1 Mlodzianoski2018
%A Mlodzianoski, Michael J.
%A Cheng-Hathaway, Paul J.
%A Bemiller, Shane M.
%A McCray, Tyler J.
%A Liu, Sheng
%A Miller, David A.
%A Lamb, Bruce T.
%A Landreth, Gary E.
%A Huang, Fang
%D 2018
%J Nature Methods
%K 3D adaptive_optics imaging microscopy psf_engineering smlm superresolution
%N 8
%P 583--586
%R 10.1038/s41592-018-0053-8
%T Active PSF shaping and adaptive optics enable volumetric localization microscopy through brain sections
%V 15
%X Application of single-molecule switching nanoscopy (SMSN) beyond the coverslip surface poses substantial challenges due to sample-induced aberrations that distort and blur single-molecule emission patterns. We combined active shaping of point spread functions and efficient adaptive optics to enable robust 3D-SMSN imaging within tissues. This development allowed us to image through 30-$\mu$m-thick brain sections to visualize and reconstruct the morphology and the nanoscale details of amyloid-$\beta$ filaments in a mouse model of Alzheimer's disease.
@article{Mlodzianoski2018,
abstract = {Application of single-molecule switching nanoscopy (SMSN) beyond the coverslip surface poses substantial challenges due to sample-induced aberrations that distort and blur single-molecule emission patterns. We combined active shaping of point spread functions and efficient adaptive optics to enable robust 3D-SMSN imaging within tissues. This development allowed us to image through 30-$\mu$m-thick brain sections to visualize and reconstruct the morphology and the nanoscale details of amyloid-$\beta$ filaments in a mouse model of Alzheimer's disease.},
added-at = {2020-04-06T13:11:22.000+0200},
author = {Mlodzianoski, Michael J. and Cheng-Hathaway, Paul J. and Bemiller, Shane M. and McCray, Tyler J. and Liu, Sheng and Miller, David A. and Lamb, Bruce T. and Landreth, Gary E. and Huang, Fang},
biburl = {https://www.bibsonomy.org/bibtex/2ee3808cb1c40d1e3a88b6df685c91b0d/kfriedl},
doi = {10.1038/s41592-018-0053-8},
file = {:C$\backslash$:/Users/Karoline/AppData/Local/Mendeley Ltd/Mendeley Desktop/Downloaded/mlodzianoski.pdf:pdf},
interhash = {01f779ff639d3b1e441b057150b2a020},
intrahash = {ee3808cb1c40d1e3a88b6df685c91b0d},
issn = {15487105},
journal = {Nature Methods},
keywords = {3D adaptive_optics imaging microscopy psf_engineering smlm superresolution},
number = 8,
pages = {583--586},
timestamp = {2020-04-06T14:08:03.000+0200},
title = {{Active PSF shaping and adaptive optics enable volumetric localization microscopy through brain sections}},
volume = 15,
year = 2018
}