Quantitative fluorescence and superresolution microscopy are often limited by insufficient data quality or artifacts. In this context, it is essential to have biologically relevant control samples to benchmark and optimize the quality of microscopes, labels and imaging conditions. Here, we exploit the stereotypic arrangement of proteins in the nuclear pore complex as in situ reference structures to characterize the performance of a variety of microscopy modalities. We created four genome edited cell lines in which we endogenously labeled the nucleoporin Nup96 with mEGFP, SNAP-tag, HaloTag or the photoconvertible fluorescent protein mMaple. We demonstrate their use (1) as three-dimensional resolution standards for calibration and quality control, (2) to quantify absolute labeling efficiencies and (3) as precise reference standards for molecular counting. These cell lines will enable the broader community to assess the quality of their microscopes and labels, and to perform quantitative, absolute measurements.
%0 Journal Article
%1 Thevathasan2019
%A Thevathasan, Jervis Vermal
%A Kahnwald, Maurice
%A Cieśliński, Konstanty
%A Hoess, Philipp
%A Peneti, Sudheer Kumar
%A Reitberger, Manuel
%A Heid, Daniel
%A Kasuba, Krishna Chaitanya
%A Hoerner, Sarah Janice
%A Li, Yiming
%A Wu, Yu Le
%A Mund, Markus
%A Matti, Ulf
%A Pereira, Pedro Matos
%A Henriques, Ricardo
%A Nijmeijer, Bianca
%A Kueblbeck, Moritz
%A Sabinina, Vilma Jimenez
%A Ellenberg, Jan
%A Ries, Jonas
%D 2019
%I Nature Publishing Group
%J Nature Methods
%K microscopy reference smlm standart superresolution
%N 10
%P 1045--1053
%R 10.1038/s41592-019-0574-9
%T Nuclear pores as versatile reference standards for quantitative superresolution microscopy
%U https://doi.org/10.1038/s41592-019-0574-9
%V 16
%X Quantitative fluorescence and superresolution microscopy are often limited by insufficient data quality or artifacts. In this context, it is essential to have biologically relevant control samples to benchmark and optimize the quality of microscopes, labels and imaging conditions. Here, we exploit the stereotypic arrangement of proteins in the nuclear pore complex as in situ reference structures to characterize the performance of a variety of microscopy modalities. We created four genome edited cell lines in which we endogenously labeled the nucleoporin Nup96 with mEGFP, SNAP-tag, HaloTag or the photoconvertible fluorescent protein mMaple. We demonstrate their use (1) as three-dimensional resolution standards for calibration and quality control, (2) to quantify absolute labeling efficiencies and (3) as precise reference standards for molecular counting. These cell lines will enable the broader community to assess the quality of their microscopes and labels, and to perform quantitative, absolute measurements.
@article{Thevathasan2019,
abstract = {Quantitative fluorescence and superresolution microscopy are often limited by insufficient data quality or artifacts. In this context, it is essential to have biologically relevant control samples to benchmark and optimize the quality of microscopes, labels and imaging conditions. Here, we exploit the stereotypic arrangement of proteins in the nuclear pore complex as in situ reference structures to characterize the performance of a variety of microscopy modalities. We created four genome edited cell lines in which we endogenously labeled the nucleoporin Nup96 with mEGFP, SNAP-tag, HaloTag or the photoconvertible fluorescent protein mMaple. We demonstrate their use (1) as three-dimensional resolution standards for calibration and quality control, (2) to quantify absolute labeling efficiencies and (3) as precise reference standards for molecular counting. These cell lines will enable the broader community to assess the quality of their microscopes and labels, and to perform quantitative, absolute measurements.},
added-at = {2020-03-23T21:12:34.000+0100},
author = {Thevathasan, Jervis Vermal and Kahnwald, Maurice and Cie{\'{s}}li{\'{n}}ski, Konstanty and Hoess, Philipp and Peneti, Sudheer Kumar and Reitberger, Manuel and Heid, Daniel and Kasuba, Krishna Chaitanya and Hoerner, Sarah Janice and Li, Yiming and Wu, Yu Le and Mund, Markus and Matti, Ulf and Pereira, Pedro Matos and Henriques, Ricardo and Nijmeijer, Bianca and Kueblbeck, Moritz and Sabinina, Vilma Jimenez and Ellenberg, Jan and Ries, Jonas},
biburl = {https://www.bibsonomy.org/bibtex/26a1600dec13c9db563b0dd7fc5cc301b/kfriedl},
doi = {10.1038/s41592-019-0574-9},
file = {:C$\backslash$:/Users/Karoline/AppData/Local/Mendeley Ltd./Mendeley Desktop/Downloaded/Thevathasan, Kahnwald - Unknown - Nuclear pores as versatile reference standards for quantitative superresolution microscopy.pdf:pdf},
interhash = {6294919cd680988e9f2dae7a8c39bd9f},
intrahash = {6a1600dec13c9db563b0dd7fc5cc301b},
issn = {15487105},
journal = {Nature Methods},
keywords = {microscopy reference smlm standart superresolution},
month = oct,
number = 10,
pages = {1045--1053},
pmid = {31562488},
publisher = {Nature Publishing Group},
timestamp = {2020-04-07T12:25:17.000+0200},
title = {{Nuclear pores as versatile reference standards for quantitative superresolution microscopy}},
url = {https://doi.org/10.1038/s41592-019-0574-9},
volume = 16,
year = 2019
}