Recent publications are listed below. For an extensive overview we kindly refer you to our publication repository DORA
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Compain G, Monsarrat C, Blagojevic J, Brillet K, Dumas P, Hammann P, et al.
Peptide-based covalent inhibitors bearing mild electrophiles to target a conserved his residue of the bacterial sliding clamp
JACS Au. 2024; 4(2): 432-440. https://doi.org/10.1021/jacsau.3c00572
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Flores-Ibarra A, Maia RNA, Olasz B, Church JR, Gotthard G, Schapiro I, et al.
Light-oxygen-voltage (LOV)-sensing domains: activation mechanism and optogenetic stimulation
Journal of Molecular Biology. 2024; 436(5): 168356 (19 pp.). https://doi.org/10.1016/j.jmb.2023.168356
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Gotthard G, Flores-Ibarra A, Carrillo M, Kepa MW, Mason TJ, Stegmann DP, et al.
Fixed-target pump–probe SFX: eliminating the scourge of light contamination
IUCrJ. 2024; 11(5): 1-13. https://doi.org/10.1107/S2052252524005591
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Huang C-Y, Aumonier S, Olieric V, Wang M
Cryo2RT: a high-throughput method for room-temperature macromolecular crystallography from cryo-cooled crystals
Acta Crystallographica Section D: Structural Biology. 2024; 80(8): 620-628. https://doi.org/10.1107/S2059798324006697
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Huang CY, Metz A, Lange R, Artico N, Potot C, Hazemann J, et al.
Fragment-based screening targeting an open form of the SARS-CoV-2 main protease binding pocket
Acta Crystallographica Section D: Structural Biology. 2024; 80: 123-136. https://doi.org/10.1107/S2059798324000329
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Just DM, Brüstle M, Guntli S, Siebold H, Widmer R, Buntschu D, et al.
Phase 0 front ends: live prototypes for SLS 2.0
Presented at: 15th international conference on synchrotron radiation instrumentation (SRI) 2024; August 26-30, 2024; Hamburg.
DORA PSI -
Mastria R, Riisnaes KJ, Bacon A, Leontis I, Lam HT, Alshehri MAS, et al.
Real time and highly sensitive sub-wavelength 2D hybrid perovskite photodetectors
Advanced Functional Materials. 2024. https://doi.org/10.1002/adfm.202401903
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Metz A, Stegmann DP, Panepucci EH, Buehlmann S, Huang CY, McAuley KE, et al.
HEIDI: an experiment-management platform enabling high-throughput fragment and compound screening
Acta Crystallographica Section D: Structural Biology. 2024; 80: 328-335. https://doi.org/10.1107/S2059798324002833
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Nievergelt P, Berliat F, McAuley KE, Dorgan CR, van Well RM, Thorn A, et al.
RNA oligomers at atomic resolution containing 1-methylpseudouridine, an essential building block of mRNA vaccines
ChemMedChem. 2024; 19(7): e202300600 (5 pp.). https://doi.org/10.1002/cmdc.202300600
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Tsujino S, Sato Y, Jia S, Kepa MW, Trampari S, Tomizaki T
Inertial mixing of acoustically levitated droplets for time-lapse protein crystallography
Droplet. 2024; 3(3): e132 (11 PP.). https://doi.org/10.1002/dro2.132
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Boland C, Huang C-Y, Shanker Kaki S, Wang M, Olieric V, Caffrey M
Se-MAG is a convenient additive for experimental phasing and structure determination of membrane proteins crystallised by the lipid cubic phase (in meso) method
Crystals. 2023; 13(9): 1402 (20 pp.). https://doi.org/10.3390/cryst13091402
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Carrillo M, Mason TJ, Karpik A, Martiel I, Kepa MW, McAuley KE, et al.
Micro-structured polymer fixed targets for serial crystallography at synchrotrons and XFELs
IUCrJ. 2023; 10(6): 678-693. https://doi.org/10.1107/S2052252523007595
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Christou N-E, Apostolopoulou V, Melo DVM, Ruppert M, Fadini A, Henkel A, et al.
Time-resolved crystallography captures light-driven DNA repair
Science. 2023; 382(6674): 1015-1020. https://doi.org/10.1126/science.adj4270
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Gruhl T, Weinert T, Rodrigues MJ, Milne CJ, Ortolani G, Nass K, et al.
Ultrafast structural changes direct the first molecular events of vision
Nature. 2023; 615: 939-944. https://doi.org/10.1038/s41586-023-05863-6
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Nguyen HTV, Chen X, Parada C, Luo A-C, Shih O, Jeng U-S, et al.
Structure of the heterotrimeric membrane protein complex FtsB-FtsL-FtsQ of the bacterial divisome
Nature Communications. 2023; 14(1): 1903 (13 pp.). https://doi.org/10.1038/s41467-023-37543-4
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Owen RL, de Sanctis D, Pearson AR, Beale JH
A standard descriptor for fixed-target serial crystallography
Acta Crystallographica Section D: Structural Biology. 2023; 79(8): 668-672. https://doi.org/10.1107/S2059798323005429
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Qin B, Li Z, Tang K, Wang T, Xie Y, Aumonier S, et al.
Identification of the SARS-unique domain of SARS-CoV-2 as an antiviral target
Nature Communications. 2023; 14(1): 3999 (13 pp.). https://doi.org/10.1038/s41467-023-39709-6
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Smith KML, Panepucci E, Kaminski JW, Aumonier S, Huang C-Y, Eris D, et al.
SDU - software for high-throughput automated data collection at the Swiss Light Source
Journal of Synchrotron Radiation. 2023; 30: 538-545. https://doi.org/10.1107/S1600577523002631
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Smithers L, Degtjarik O, Weichert D, Huang C-Y, Boland C, Bowen K, et al.
Structure snapshots reveal the mechanism of a bacterial membrane lipoprotein N-acyltransferase
Science Advances. 2023; 9(26): eadf5799 (17 pp.). https://doi.org/10.1126/sciadv.adf5799
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Stegmann DP, Steuber J, Fritz G, Wojdyla JA, Sharpe ME
Fast fragment and compound screening pipeline at the Swiss Light Source
In: Methods in enzymology. sine loco: Elsevier; 2023:235-284. https://doi.org/10.1016/bs.mie.2023.08.005
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Wranik M, Kepa MW, Beale EV, James D, Bertrand Q, Weinert T, et al.
A multi-reservoir extruder for time-resolved serial protein crystallography and compound screening at X-ray free-electron lasers
Nature Communications. 2023; 14(1): 7956 (12 pp.). https://doi.org/10.1038/s41467-023-43523-5
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Wranik M, Weinert T, Slavov C, Masini T, Furrer A, Gaillard N, et al.
Watching the release of a photopharmacological drug from tubulin using time-resolved serial crystallography
Nature Communications. 2023; 14(1): 903 (12 pp.). https://doi.org/10.1038/s41467-023-36481-5
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Abiko LA, Dias Teixeira R, Engilberge S, Grahl A, Mühlethaler T, Sharpe T, et al.
Filling of a water-free void explains the allosteric regulation of the β1-adrenergic receptor by cholesterol
Nature Chemistry. 2022; 14: 1133-1141. https://doi.org/10.1038/s41557-022-01009-9
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Alsarraf HMAB, Ung KL, Johansen MD, Dimon J, Olieric V, Kremer L, et al.
Biochemical, structural, and functional studies reveal that MAB_4324c from Mycobacterium abscessus is an active tandem repeat N‐acetyltransferase
FEBS Letters. 2022; 596(12): 1516-1532. https://doi.org/10.1002/1873-3468.14360
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Aumonier S, Engilberge S, Caramello N, von Stetten D, Gotthard G, Leonard GA, et al.
Slow protein dynamics probed by time-resolved oscillation crystallography at room temperature
IUCrJ. 2022; 9(6): 756-767. https://doi.org/10.1107/S2052252522009150
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Bleuler-Martinez S, Varrot A, Olieric V, Schubert M, Vogt E, Fetz C, et al.
Structure–function relationship of a novel fucoside-binding fruiting body lectin from Coprinopsis cinerea exhibiting nematotoxic activity
Glycobiology. 2022; 32(7): 600-615. https://doi.org/10.1093/glycob/cwac020
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Cellini A, Shankar MK, Wahlgren WY, Nimmrich A, Furrer A, James D, et al.
Structural basis of the radical pair state in photolyases and cryptochromes
Chemical Communications. 2022; 58(31): 4889-4892. https://doi.org/10.1039/D2CC00376G
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Collu G, Bierig T, Krebs A-S, Engilberge S, Varma N, Guixà-González R, et al.
Chimeric single α-helical domains as rigid fusion protein connections for protein nanotechnology and structural biology
Structure. 2022; 30(1): 95-106. https://doi.org/10.1016/j.str.2021.09.002
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Huang C-Y, Aumonier S, Engilberge S, Eris D, Smith KML, Leonarski F, et al.
Probing ligand binding of endothiapepsin by 'temperature-resolved' macromolecular crystallography
Acta Crystallographica Section D: Structural Biology. 2022; 78: 964-974. https://doi.org/10.1107/S205979832200612X
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Kaminski JW, Vera L, Stegmann DP, Vering J, Eris D, Smith KML, et al.
Fast fragment- and compound-screening pipeline at the Swiss Light Source
Acta Crystallographica Section D: Structural Biology. 2022; 78: 328-336. https://doi.org/10.1107/S2059798322000705
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Kepa MW, Tomizaki T, Sato Y, Ozerov D, Sekiguchi H, Yasuda N, et al.
Acoustic levitation and rotation of thin films and their application for room temperature protein crystallography
Scientific Reports. 2022; 12: 5349 (14 pp.). https://doi.org/10.1038/s41598-022-09167-z
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Mertens V, Abi Saad MJ, Coudevylle N, Wälti MA, Finke A, Marsh M, et al.
Elucidation of a nutlin-derivative-HDM2 complex structure at the interaction site by NMR molecular replacement: a straightforward derivation
Journal of Magnetic Resonance Open. 2022; 10-11: 100032 (5 pp.). https://doi.org/10.1016/j.jmro.2022.100032
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Moreno-Chicano T, Carey LM, Axford D, Beale JH, Doak RB, Duyvesteyn HME, et al.
Complementarity of neutron, XFEL and synchrotron crystallography for defining the structures of metalloenzymes at room temperature
IUCrJ. 2022; 9(5): 610-624. https://doi.org/10.1107/S2052252522006418
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Mous S, Gotthard G, Ehrenberg D, Sen S, Weinert T, Johnson PJM, et al.
Dynamics and mechanism of a light-driven chloride pump
Science. 2022; 375(6583): 845-851. https://doi.org/10.1126/science.abj6663
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Pedrini B, Finke AD, Marsh M, Luporini P, Vallesi A, Alimenti C
Crystal structure of the pheromone Er-13 from the ciliate Euplotes raikovi, with implications for a protein-protein association model in pheromone/receptor interactions
Journal of Structural Biology. 2022; 214(1): 107812 (10 pp.). https://doi.org/10.1016/j.jsb.2021.107812
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Qiao Z, Kong Q, Tee WT, Lim ARQ, Teo MX, Olieric V, et al.
Molecular basis of the key regulator WRINKLED1 in plant oil biosynthesis
Science Advances. 2022; 8(34): eabq1211 (10 pp.). https://doi.org/10.1126/sciadv.abq1211
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Wang H, Mörman C, Sternke-Hoffmann R, Huang CY, Prota A, Ma P, et al.
Cu2+ ions modulate the interaction between α-synuclein and lipid membranes
Journal of Inorganic Biochemistry. 2022; 236: 111945 (10 pp.). https://doi.org/10.1016/j.jinorgbio.2022.111945
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Xu Q, Sun N, Xiao Q, Huang C-ying, Xu M, Zhang W, et al.
The crystal structure of MreC provides insights into polymer formation
FEBS Open Bio. 2022; 12(2): 340-348. https://doi.org/10.1002/2211-5463.13296
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Ashton A, Augustin S, Babic A, Celcer T, Ebner SG, Egli S, et al.
Conceptual design report on controls and science IT for the SLS 2.0 upgrade project
Villigen PSI, Switzerland: Paul Scherrer Institut; 2021. PSI Bericht: 21-03.
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Beale JH, Marsh ME
Optimizing the growth of endothiapepsin crystals for serial crystallography experiments
Journal of Visualized Experiments. 2021; 168: e61896 (30 pp.). https://doi.org/10.3791/61896
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Braun H, Garvey T, Jörg M, Ashton A, Willmott P, Kobler R, et al.
SLS 2.0 storage ring. Technical design report
Villigen PSI, Switzerland: Paul Scherrer Institut; 2021. PSI Bericht: 21-02.
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Butryn A, Simon PS, Aller P, Hinchliffe P, Massad RN, Leen G, et al.
An on-demand, drop-on-drop method for studying enzyme catalysis by serial crystallography
Nature Communications. 2021; 12(1): 4461 (7 pp.). https://doi.org/10.1038/s41467-021-24757-7
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Cinquino M, Fieramosca A, Mastria R, Polimeno L, Moliterni A, Olieric V, et al.
Managing growth and dimensionality of quasi 2D perovskite single-crystalline flakes for tunable excitons orientation
Advanced Materials. 2021; 33(48): 2102326 (9 pp.). https://doi.org/10.1002/adma.202102326
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Dhanabalan B, Biffi G, Moliterni A, Olieric V, Giannini C, Saleh G, et al.
Engineering the optical emission and robustness of metal-halide layered perovskites through ligand accommodation
Advanced Materials. 2021; 33(13): 2008004 (11 pp.). https://doi.org/10.1002/adma.202008004
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Gao X, Zhu K, Qin B, Olieric V, Wang M, Cui S
Crystal structure of SARS-CoV-2 Orf9b in complex with human TOM70 suggests unusual virus-host interactions
Nature Communications. 2021; 12(1): 2843 (9 pp.). https://doi.org/10.1038/s41467-021-23118-8
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Gao X, Qin B, Chen P, Zhu K, Hou P, Wojdyla JA, et al.
Crystal structure of SARS-CoV-2 papain-like protease
Acta Pharmaceutica Sinica B. 2021; 11(1): 237-245. https://doi.org/10.1016/j.apsb.2020.08.014
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Gao C, Stavenhagen K, Eckmair B, McKitrick TR, Mehta AY, Matsumoto Y, et al.
Differential recognition of oligomannose isomers by glycan-binding proteins involved in innate and adaptive immunity
Science Advances. 2021; 7(24): eabf6834 (12 pp.). https://doi.org/10.1126/sciadv.abf6834
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Hahn CJ, Lemaire ON, Kahnt J, Engilberge S, Wegener G, Wagner T
Crystal structure of a key enzyme for anaerobic ethane activation
Science. 2021; 373(6550): 118-121. https://doi.org/10.1126/science.abg1765
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Iorio A, Roche J, Engilberge S, Coquelle N, Girard E, Sterpone F, et al.
Biochemical, structural and dynamical studies reveal strong differences in the thermal-dependent allosteric behavior of two extremophilic lactate dehydrogenases
Journal of Structural Biology. 2021; 213(3): 107769 (11 pp.). https://doi.org/10.1016/j.jsb.2021.107769
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Kepa MW, Tomizaki T, Tsujino S
Development of on-demand sample loading of ultrasound acoustic levitators by focused acoustic radiation
In: IEEE international ultrasonics symposium (IUS 2021). Danvers, MA: IEEE; 2021:(3 pp.). https://doi.org/10.1109/IUS52206.2021.9593735
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Li H, Huang C-Y, Govorunova EG, Sineshchekov OA, Yi A, Rothschild KJ, et al.
The crystal structure of bromide-bound GtACR1 reveals a pre-activated state in the transmembrane anion tunnel
eLife. 2021; 10: e65903 (14 pp.). https://doi.org/10.7554/eLife.65903
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Martiel I, Beale JH, Karpik A, Huang C-Y, Vera L, Olieric N, et al.
Versatile microporous polymer-based supports for serial macromolecular crystallography
Acta Crystallographica Section D: Structural Biology. 2021; 77(9): 1153-1167. https://doi.org/10.1107/S2059798321007324
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Monsarrat C, Compain G, André C, Engilberge S, Martiel I, Oliéric V, et al.
Iterative structure-based optimization of short peptides targeting the bacterial sliding clamp
Journal of Medicinal Chemistry. 2021; 64(23): 17063-17078. https://doi.org/10.1021/acs.jmedchem.1c00918
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Mühlethaler T, Gioia D, Prota AE, Sharpe ME, Cavalli A, Steinmetz MO
Comprehensive analysis of binding sites in tubulin
Angewandte Chemie International Edition. 2021; 60(24): 13331-13342. https://doi.org/10.1002/anie.202100273
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Nasrallah C, Cannone G, Briot J, Rottier K, Berizzi AE, Huang CY, et al.
Agonists and allosteric modulators promote signaling from different metabotropic glutamate receptor 5 conformations
Cell Reports. 2021; 36(9): 109648 (19 pp.). https://doi.org/10.1016/j.celrep.2021.109648
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Nass K, Bacellar C, Cirelli C, Dworkowski F, Gevorkov Y, James D, et al.
Pink-beam serial femtosecond crystallography for accurate structure-factor determination at an X-ray free-electron laser
IUCrJ. 2021; 8: 905-920. https://doi.org/10.1107/S2052252521008046
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Ni X, Schröder M, Olieric V, Sharpe ME, Hernandez-Olmos V, Proschak E, et al.
Structural insights into plasticity and discovery of remdesivir metabolite GS-441524 binding in SARS-CoV-2 macrodomain
ACS Medicinal Chemistry Letters. 2021; 12(4): 603-609. https://doi.org/10.1021/acsmedchemlett.0c00684
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Olatunji S, Bowen K, Huang CY, Weichert D, Singh W, Tikhonova IG, et al.
Structural basis of the membrane intramolecular transacylase reaction responsible for lyso-form lipoprotein synthesis
Nature Communications. 2021; 12(1): 4254 (14 pp.). https://doi.org/10.1038/s41467-021-24475-0
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Palmerini V, Monzani S, Laurichesse Q, Loudhaief R, Mari S, Cecatiello V, et al.
Drosophila TNFRs Grindelwald and Wengen bind Eiger with different affinities and promote distinct cellular functions
Nature Communications. 2021; 12(1): 2070 (12 pp.). https://doi.org/10.1038/s41467-021-22080-9
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Polimeno L, Lerario G, De Giorgi M, De Marco L, Dominici L, Todisco F, et al.
Tuning of the Berry curvature in 2D perovskite polaritons
Nature Nanotechnology. 2021; 16: 1349-1354. https://doi.org/10.1038/s41565-021-00977-2
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Ramberg KO, Engilberge S, Skorek T, Crowley PB
Facile fabrication of protein-macrocycle frameworks
Journal of the American Chemical Society. 2021; 143(4): 1896-1907. https://doi.org/10.1021/jacs.0c10697
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Ramos J, Laux V, Haertlein M, Boeri Erba E, McAuley KE, Forsyth VT, et al.
Structural insights into protein folding, stability and activity using in vivo perdeuteration of hen egg-white lysozyme
IUCrJ. 2021; 8: 372-386. https://doi.org/10.1107/S2052252521001299
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Scott DE, Francis-Newton NJ, Marsh ME, Coyne AG, Fischer G, Moschetti T, et al.
A small-molecule inhibitor of the BRCA2-RAD51 interaction modulates RAD51 assembly and potentiates DNA damage-induced cell death
Cell Chemical Biology. 2021; 28(6): 835-847.e5. https://doi.org/10.1016/j.chembiol.2021.02.006
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Sharpe ME, Wojdyla JA
Fragment-screening and automation at the Swiss Light Source macromolecular crystallography beamlines
Nihon Kessho Gakkaishi. 2021; 63(3): 232-235. https://doi.org/10.5940/jcrsj.63.232
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Sutanto F, Shaabani S, Oerlemans R, Eris D, Patil P, Hadian M, et al.
Combining high-throughput synthesis and high-throughput protein crystallography for accelerated hit identification
Angewandte Chemie International Edition. 2021; 60(33): 18231-18239. https://doi.org/10.1002/anie.202105584
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Toomey B, Han X, Dong CD, Edward V, Kaminski JW, Shankar S
Characterization of phases and orientations of micro-structured materials Using computational crystallography
In: Shankar S, Muller R, Dunning T, Chen GH, eds. Computational materials, chemistry, and biochemistry: from bold initiatives to the last mile. In honor of William A. Goddard’s contributions to science and engineering. Springer series in materials science. Cham: Springer Nature; 2021:213-231. https://doi.org/10.1007/978-3-030-18778-1_11
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de Wijn R, Rollet K, Olieric V, Hennig O, Thome N, Noûs C, et al.
Crystallization and structural determination of an enzyme: substrate complex by serial crystallography in a versatile microfluidic chip
Journal of Visualized Experiments. 2021; 2021(169): e61972 (15 pp.). https://doi.org/10.3791/61972
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Assmann GM, Wang M, Diederichs K
Making a difference in multi-data-set crystallography: simple and deterministic data-scaling/selection methods
Acta Crystallographica Section D: Structural Biology. 2020; 76: 636-652. https://doi.org/10.1107/S2059798320006348
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Beale JH
Macromolecular X-ray crystallography: soon to be a road less travelled?
Acta Crystallographica Section D: Structural Biology. 2020; 76(5): 400-405. https://doi.org/10.1107/S2059798320004660
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Bedi RK, Huang D, Wiedmer L, Li Y, Dolbois A, Wojdyla JA, et al.
Selectively disrupting m6A-dependent protein-RNA interactions with fragments
ACS Chemical Biology. 2020; 15(3): 618-625. https://doi.org/10.1021/acschembio.9b00894
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Bernstein HJ, Förster A, Bhowmick A, Brewster AS, Brockhauser S, Gelisio L, et al.
Gold standard for macromolecular crystallography diffraction data
IUCrJ. 2020; 7(5): 784-792. https://doi.org/10.1107/S2052252520008672
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Bu W, Levitskaya Z, Loh ZY, Jin S, Basu S, Ero R, et al.
Structural basis of human full-length kindlin-3 homotrimer in an auto-inhibited state
PLoS Biology. 2020; 18(7): e3000755 (24 pp.). https://doi.org/10.1371/journal.pbio.3000755
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Cheng R, Huang C-Y, Hennig M, Nar H, Schnapp G
In situ crystallography as an emerging method for structure solution of membrane proteins: the case of CCR2A
FEBS Journal. 2020; 287(5): 866-873. https://doi.org/10.1111/febs.15098
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Cinquino M, Polimeno L, Lerario G, De Giorgi M, Moliterni A, Olieric V, et al.
One-step synthesis at room temperature of low dimensional perovskite single crystals with high optical quality
Journal of Luminescence. 2020; 221: 117079 (8 pp.). https://doi.org/10.1016/j.jlumin.2020.117079
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Crack JC, Amara P, Volbeda A, Mouesca J-M, Rohac R, Pellicer Martinez MT, et al.
Electron and proton transfers modulate DNA binding by the transcription regulator RsrR
Journal of the American Chemical Society. 2020; 142(11): 5104-5116. https://doi.org/10.1021/jacs.9b12250
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Engilberge S, Wagner T, Carpentier P, Girard E, Shima S
Krypton-derivatization highlights O2-channeling in a four-electron reducing oxidase
Chemical Communications. 2020; 56(74): 10863-10866. https://doi.org/10.1039/d0cc04557h
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Fadini A, Reiche S, Nass K, van Thor JJ
Applications and limits of time-to-energy mapping of protein crystal diffraction using energy-chirped polychromatic XFEL pulses
Applied Sciences. 2020; 10(7): 2599 (18 pp.). https://doi.org/10.3390/app10072599
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Gao X, Zhu K, Wojdyl JA, Chen P, Qin B, Li Z, et al.
Crystal structure of the NS3-like helicase from Alongshan virus
IUCrJ. 2020; 7(3): 375-382. https://doi.org/10.1107/S2052252520003632
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Görlich S, Samuel AJ, Best RJ, Seidel R, Vacelet J, Leonarski FK, et al.
Natural hybrid silica/protein superstructure at atomic resolution
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2020; 117(49): 31088-31093. https://doi.org/10.1073/pnas.2019140117
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Huang C-Y, Meier N, Caffrey M, Wang M, Olieric V
3D-printed holders for in meso in situ fixed-target serial X-ray crystallography
Journal of Applied Crystallography. 2020; 53: 854-859. https://doi.org/10.1107/S1600576720002897
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Huang C-Y, Olieric V, Caffrey M, Wang M
In meso in situ serial X-Ray crystallography (IMISX): a protocol for membrane protein structure determination at the Swiss Light Source
In: Perez C, Maier T, eds. Expression, purification, and structural biology of membrane proteins. Methods in molecular biology. New York: Humana; 2020:293-319. https://doi.org/10.1007/978-1-0716-0373-4_20
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Huwald D, Duda S, Gasper R, Olieric V, Hofmann E, Hemschemeier A
Distinctive structural properties of THB11, a pentacoordinate Chlamydomonas reinhardtii truncated hemoglobin with N- and C-terminal extensions
Journal of Biological Inorganic Chemistry. 2020; 25: 267-283. https://doi.org/10.1007/s00775-020-01759-2
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Karpik A, Martiel I, Kristiansen PM, Padeste C
Fabrication of ultrathin suspended polymer membranes as supports for serial protein crystallography
Micro and Nano Engineering. 2020; 7: 100053 (6 pp.). https://doi.org/10.1016/j.mne.2020.100053
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Leonarski F, Mozzanica A, Brückner M, Lopez-Cuenca C, Redford S, Sala L, et al.
JUNGFRAU detector for brighter x-ray sources: solutions for IT and data science challenges in macromolecular crystallography
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