% 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{Ayyer:453632,
author = {Ayyer, Kartik and Paulraj, Lourdu Xavier and Bielecki,
Johan and Shen, Zhou and Daurer, Benedikt J. and Samanta,
Amit K. and Awel, Salah and Bean, Richard and Barty, Anton
and Bergemann, Martin and Ekeberg, Tomas and Estillore,
Armando D. and Fangohr, Hans and Giewekemeyer, Klaus and
Hunter, Mark S. and Karnevskiy, Mikhail and Kirian, Richard
and Kirkwood, Henry and Kim, Yoonhee and Koliyadu, Jayanath
and Lange, Holger and Letrun, Romain and Luebke, Jannik and
Michelat, Thomas and Morgan, Andrew J. and Roth, Nils and
Sato, Tokushi and Sikorski, Marcin and Schulz, Florian and
Spence, John C. H. and Vagovic, Patrik and Wollweber, Tamme
and Worbs, Lena and Yefanov, Oleksandr and Zhuang, Yulong
and Maia, Filipe R. N. C. and Horke, Daniel A. and Küpper,
Jochen and Loh, N. Duane and Mancuso, Adrian P. and Chapman,
Henry N.},
title = {3{D} diffractive imaging of nanoparticle ensembles using an
x-ray laser},
journal = {Optica},
volume = {8},
number = {1},
issn = {2334-2536},
address = {Washington, DC},
publisher = {OSA},
reportid = {PUBDB-2021-00075},
pages = {15 - 23},
year = {2021},
note = {5 main figures, 6 supplementary figures, 2 supplementary
movies (link in document)},
abstract = {Single particle imaging at x-ray free electron lasers
(XFELs) has the potential to determine the structure and
dynamics of single biomolecules at room temperature. Two
major hurdles have prevented this potential from being
reached, namely, the collection of sufficient high-quality
diffraction patterns and robust computational purification
to overcome structural heterogeneity. We report the breaking
of both of these barriers using gold nanoparticle test
samples, recording around 10 million diffraction patterns at
the European XFEL and structurally and orientationally
sorting the patterns to obtain better than 3-nm-resolution
3D reconstructions for each of four samples. With these new
developments, integrating advancements in x-ray sources,
fast-framing detectors, efficient sample delivery, and data
analysis algorithms, we illuminate the path towards
sub-nanometer biomolecular imaging. The methods developed
here can also be extended to characterize ensembles that are
inherently diverse to obtain their full structural
landscape.},
cin = {CFEL-I / FS-CFEL-1 / FS-CFEL-CMI / UNI/CUI / UNI/EXP},
ddc = {620},
cid = {I:(DE-H253)CFEL-I-20161114 / I:(DE-H253)FS-CFEL-1-20120731
/ I:(DE-H253)FS-CFEL-CMI-20220405 /
$I:(DE-H253)UNI_CUI-20121230$ /
$I:(DE-H253)UNI_EXP-20120731$},
pnm = {633 - Life Sciences – Building Blocks of Life: Structure
and Function (POF4-633) / DFG project 194651731 - EXC 1074:
Hamburger Zentrum für ultraschnelle Beobachtung (CUI):
Struktur, Dynamik und Kontrolle von Materie auf atomarer
Skala (194651731) / DFG project 390715994 - EXC 2056: CUI:
Advanced Imaging of Matter (390715994) / COMOTION -
Controlling the Motion of Complex Molecules and Particles
(614507)},
pid = {G:(DE-HGF)POF4-633 / G:(GEPRIS)194651731 /
G:(GEPRIS)390715994 / G:(EU-Grant)614507},
experiment = {EXP:(DE-H253)XFEL-Exp-20150101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000610085000003},
doi = {10.1364/OPTICA.410851},
url = {https://bib-pubdb1.desy.de/record/453632},
}