Literature DB >> 28370211

A protocol for registration and correction of multicolour STED superresolution images.

E Hebisch1, E Wagner2,3, V Westphal1, J J Sieber4, S E Lehnart2,3.   

Abstract

Multicolour fluorescence imaging by STimulated Emission Depletion (STED) superresolution microscopy with doughnut-shaped STED laser beams based on different wavelengths for each colour channel requires precise image registration. This is especially important when STED imaging is used for co-localisation studies of two or more native proteins in biological specimens to analyse nanometric subcellular spatial arrangements. We developed a robust postprocessing image registration protocol, with the aim to verify and ultimately optimise multicolour STED image quality. Importantly, this protocol will support any subsequent quantitative localisation analysis at nanometric scales. Henceforth, using an approach that registers each colour channel present during STED imaging individually, this protocol reliably corrects for optical aberrations and inadvertent sample drift. To achieve the latter goal, the protocol combines the experimental sample information, from corresponding STED and confocal images using the same optical beam path and setup, with that of an independent calibration sample. As a result, image registration is based on a strategy that maximises the cross-correlation between sequentially acquired images of the experimental sample, which are strategically combined by the protocol. We demonstrate the general applicability of the image registration protocol by co-staining of the ryanodine receptor calcium release channel in primary mouse cardiomyocytes. To validate this new approach, we identify user-friendly criteria, which - if fulfilled - support optimal image registration. In summary, we introduce a new method for image registration and rationally based postprocessing steps through a highly standardised protocol for multicolour STED imaging, which directly supports the reproducibility of protein co-localisation analyses. Although the reference protocol is discussed exemplarily for two-colour STED imaging, it can be readily expanded to three or more colours and STED channels.
© 2017 The Authors. Journal of Microscopy published by JohnWiley & Sons Ltd on behalf of Royal Microscopical Society.

Entities:  

Keywords:  Image registration; STED microscopy; multicolour imaging; ryanodine receptor; targeted superresolution microscopy

Mesh:

Substances:

Year:  2017        PMID: 28370211     DOI: 10.1111/jmi.12556

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  5 in total

1.  A simple empirical algorithm for optimising depletion power and resolution for dye and system specific STED imaging.

Authors:  Christian A Combs; Dan L Sackett; Jay R Knutson
Journal:  J Microsc       Date:  2019-05-09       Impact factor: 1.758

2.  Calpain cleavage of Junctophilin-2 generates a spectrum of calcium-dependent cleavage products and DNA-rich NT1-fragment domains in cardiomyocytes.

Authors:  Gunnar Weninger; Tatiana Pochechueva; Dana El Chami; Xiaojing Luo; Tobias Kohl; Sören Brandenburg; Henning Urlaub; Kaomei Guan; Christof Lenz; Stephan E Lehnart
Journal:  Sci Rep       Date:  2022-06-20       Impact factor: 4.996

Review 3.  Advances in fluorescence microscopy techniques to study kidney function.

Authors:  Suman Ranjit; Luca Lanzanò; Andrew E Libby; Enrico Gratton; Moshe Levi
Journal:  Nat Rev Nephrol       Date:  2020-09-18       Impact factor: 28.314

4.  Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes.

Authors:  Ivona Kubalová; Alžběta Němečková; Klaus Weisshart; Eva Hřibová; Veit Schubert
Journal:  Int J Mol Sci       Date:  2021-02-14       Impact factor: 5.923

5.  Evaluation of sted super-resolution image quality by image correlation spectroscopy (QuICS).

Authors:  Elena Cerutti; Morgana D'Amico; Isotta Cainero; Gaetano Ivan Dellino; Mario Faretta; Giuseppe Vicidomini; Pier Giuseppe Pelicci; Paolo Bianchini; Alberto Diaspro; Luca Lanzanò
Journal:  Sci Rep       Date:  2021-10-21       Impact factor: 4.379

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.