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Is Radiation Damage the Limiting Factor in Single Particle Imaging with X-ray Free-Electron Lasers?
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.ORCID-id: 0000-0002-0021-4354
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik.ORCID-id: 0000-0001-7328-0400
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Molekyl- och kondenserade materiens fysik. Center for Free-Electron Laser Science, DESY, Hamburg, Germany .
School of Science, RMIT University, Melbourne, Australia.
2019 (Engelska)Ingår i: Structural Dynamics, E-ISSN 2329-7778, Vol. 6, artikel-id 044103Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The prospect of single particle imaging with atomic resolution is one of the scientific drivers for the development of X-ray free-electron lasers. The assumption since the beginning has been that damage to the sample caused by intense X-ray pulses is one of the limiting factors of coherent diffractive imaging of single particles and that X-ray pulses need to be as short as possible. Based on molecular dynamics simulations of proteins in X-ray fields of various durations (5 fs, 25 fs and 50 fs), we show that the noise in the diffracted signal caused by radiation damage is less than what can be expected from other sources, such as sample inhomogeneity and X-ray shot-to-shot variations. These findings show a different aspect of the feasibility of single particle imaging using free-electron lasers, where employing X-ray pulses of longer durations could still provide a useful diffraction signal above the noise due to the Coulomb explosion.

Ort, förlag, år, upplaga, sidor
2019. Vol. 6, artikel-id 044103
Nyckelord [en]
X-ray free electron laser, XFEL, X-ray diffraction, Ultrafast imaging, Coherent diffractive imaging, CDI, Single particle imaging, Computer simulation, Molecular dynamics, GROMACS, Radiation damage, Coulomb explosion
Nationell ämneskategori
Biofysik
Identifikatorer
URN: urn:nbn:se:uu:diva-382432DOI: 10.1063/1.5098309ISI: 000492051300004PubMedID: 31463335OAI: oai:DiVA.org:uu-382432DiVA, id: diva2:1306890
Forskningsfinansiär
VetenskapsrådetStiftelsen för strategisk forskning (SSF)Stiftelsen för internationalisering av högre utbildning och forskning (STINT)Swedish National Infrastructure for Computing (SNIC), snic2016-7-61Tillgänglig från: 2019-04-25 Skapad: 2019-04-25 Senast uppdaterad: 2019-11-15Bibliografiskt granskad
Ingår i avhandling
1. Simulations of Biomolecular Fragmentation and Diffraction with Ultrafast X-ray Lasers
Öppna denna publikation i ny flik eller fönster >>Simulations of Biomolecular Fragmentation and Diffraction with Ultrafast X-ray Lasers
2019 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Studies of biomolecules have recently seen substantial developments. New X-ray lasers allow for high-resolution imaging of protein crystals too small for conventional X-ray crystallography. Even structures of single particles have been determined at lower resolutions with these new sources. The secret lies in the ultrashort high-intensity pulses, which allow for diffraction and retrieval of structural information before the sample gets fragmented. However, the attainable resolution is still limited, in particular when imaging non-crystalline samples, making further advancements highly desired. In this thesis, some of the resolution-limiting obstacles facing single particle imaging (SPI) of proteins are studied in silico.

As the X-ray pulse interacts with injected single molecules, their spatial orientation is generally unknown. Recovering the orientation is essential to the structure determination process, and currently nontrivial. Molecular dynamics simulations show that the Coulomb explosion due to intense X-ray ionization could provide information pertaining to the original orientation. Used in conjunction with current methods, this would lead to an enhanced three-dimensional reconstruction of the protein.

Radiation damage and sample heterogeneity constitute considerable sources of noise in SPI. Pulse durations are presently not brief enough to circumvent damage, causing the sample to deteriorate during imaging, and the accuracy of the averaged diffraction pattern is impaired by structural variations. The extent of these effects were studied by molecular dynamics. Our findings suggest that radiation damage in terms of ionization and atomic displacement promotes a gating mechanism, benefiting imaging with longer pulses. Because of this, sample heterogeneity poses a greater challenge and efforts should be made to minimize its impact.

X-ray lasers generate pulses with a stochastic temporal distribution of photons, affecting the achievable resolution on a  pulse-to-pulse basis. Plasma simulations were performed to investigate how these fluctuations influence the damage dynamics and the diffraction signal. The results reveal that structural information is particularly well-preserved if the temporal distribution is skewed such that most photons are concentrated at the beginning.

While many obstacles remain, the prospect of atomic-resolution SPI is drawing ever closer. This thesis is but one of the stepping stones necessary to get us there. Once we do, the possibilities are limitless.

Ort, förlag, år, upplaga, sidor
Uppsala: Acta Universitatis Upsaliensis, 2019. s. 84
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1815
Nyckelord
X-ray free-electron laser, X-ray imaging, Single particle imaging, Computer simulation, Radiation damage, Molecular dynamics, Diffraction theory, Coulomb explosion, Sample heterogeneity, Diffractive noise, XFEL, SPI
Nationell ämneskategori
Biofysik
Forskningsämne
Fysik med inriktning mot biofysik
Identifikatorer
urn:nbn:se:uu:diva-382441 (URN)978-91-513-0669-8 (ISBN)
Disputation
2019-06-14, Häggsalen, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 10:15 (Engelska)
Opponent
Handledare
Forskningsfinansiär
Vetenskapsrådet
Tillgänglig från: 2019-05-23 Skapad: 2019-04-28 Senast uppdaterad: 2019-06-18

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