3D particle averaging and detection of macromolecular symmetry in localization microscopy (vol 12, 2847, 2021)

被引:0
作者
Heydarian, Hamidreza
Joosten, Maarten
Przybylski, Adrian
Schueder, Florian
Jungmann, Ralf
van Werkhoven, Ben
Keller-Findeisen, Jan
Ries, Jonas
Stallinga, Sjoerd
Bates, Mark
Rieger, Bernd
机构
[1] Department of Imaging Physics, Delft University of Technology, Delft
[2] Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Göttingen
[3] Department of Physics and Center for Nanoscience, Ludwig Maximilian University, Munich
[4] Max Planck Institute of Biochemistry, Martinsried
[5] Netherlands eScience Center, Amsterdam
[6] Cell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Heidelberg
基金
欧洲研究理事会;
关键词
D O I
10.1038/s41467-021-23767-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single molecule localization microscopy offers in principle resolution down to the molecular level, but in practice this is limited primarily by incomplete fluorescent labeling of the structure. This missing information can be completed by merging information from many structurally identical particles. In this work, we present an approach for 3D single particle analysis in localization microscopy which hugely increases signal-to-noise ratio and resolution and enables determining the symmetry groups of macromolecular complexes. Our method does not require a structural template, and handles anisotropic localization uncertainties. We demonstrate 3D reconstructions of DNA-origami tetrahedrons, Nup96 and Nup107 subcomplexes of the nuclear pore complex acquired using multiple single molecule localization microscopy techniques, with their structural symmetry deducted from the data. © 2021, The Author(s).
引用
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页数:1
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