% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Henderikx:1024123,
author = {Henderikx, Rene J. M. and Mann, Daniel and Domanska, Aušra
and Dong, Jing and Shahzad, Saba and Lak, Behnam and
Filopoulou, Aikaterini and Ludig, Damian and Grininger,
Martin and Momoh, Jeffrey and Laanto, Elina and Oksanen,
Hanna M. and Bisikalo, Kyrylo and Williams, Pamela A. and
Butcher, Sarah J. and Peters, Peter J. and Beulen, Bart W.
A. M. M.},
title = {{V}itro{J}et: new features and case studies},
journal = {Acta crystallographica / Section D},
volume = {80},
number = {4},
issn = {0907-4449},
address = {Bognor Regis},
publisher = {Wiley},
reportid = {FZJ-2024-01972},
pages = {D80},
year = {2024},
abstract = {Single-particle cryo-electron microscopy has become a
widely adopted methodin structural biology due to many
recent technological advances in microscopes,detectors and
image processing. Before being able to inspect a biological
samplein an electron microscope, it needs to be deposited in
a thin layer on a grid andrapidly frozen. The VitroJet was
designed with this aim, as well as avoiding thedelicate
manual handling and transfer steps that occur during the
conventionalgrid-preparation process. Since its creation,
numerous technical developmentshave resulted in a device
that is now widely utilized in multiple
laboratoriesworldwide. It features plasma treatment,
low-volume sample deposition throughpin printing, optical
ice-thickness measurement and cryofixation of
pre-clippedAutogrids through jet vitrification. This paper
presents recent technicalimprovements to the VitroJet and
the benefits that it brings to the cryo-EMworkflow. A wide
variety of applications are shown: membrane
proteins,nucleosomes, fatty-acid synthase, Tobacco mosaic
virus, lipid nanoparticles, tickborneencephalitis viruses
and bacteriophages. These case studies illustrate
theadvancement of the VitroJet into an instrument that
enables accurate controland reproducibility, demonstrating
its suitability for time-efficient cryo-EMstructure
determination.},
cin = {ER-C-3},
ddc = {530},
cid = {I:(DE-Juel1)ER-C-3-20170113},
pnm = {5352 - Understanding the Functionality of Soft Matter and
Biomolecular Systems (POF4-535) / 5241 - Molecular
Information Processing in Cellular Systems (POF4-524)},
pid = {G:(DE-HGF)POF4-5352 / G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
pubmed = {38488730},
UT = {WOS:001208750500002},
doi = {10.1107/S2059798324001852},
url = {https://juser.fz-juelich.de/record/1024123},
}