The list below shows the publications before 2020. You can find the publications from 2020 onwards here.
Publication Pre-2020
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del Barrio J, Liu J, Brady RA, Tan CSY, Chiodini S, Ricci M, et al.
Emerging two-dimensional crystallization of cucurbit[8]uril complexes: from supramolecular polymers to nanofibers
Journal of the American Chemical Society. 2019; 141(36): 14021-14025. https://doi.org/10.1021/jacs.9b07506
DORA PSI
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Abela E, Missimer JH, Pastore-Wapp M, Krammer W, Wiest R, Weder BJ
Early prediction of long-term tactile object recognition performance after sensorimotor stroke
Cortex. 2019; 115: 264-279. https://doi.org/10.1016/j.cortex.2019.01.018
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Akhmanova A, Steinmetz MO
Microtubule minus-end regulation at a glance
Journal of Cell Science. 2019; 132(11): jcs227850 (7 pp.). https://doi.org/10.1242/jcs.227850
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Atherton J, Luo Y, Xiang S, Yang C, Rai A, Jiang K, et al.
Structural determinants of microtubule minus end preference in CAMSAP CKK domains
Nature Communications. 2019; 10(1): 5236 (16 pp.). https://doi.org/10.1038/s41467-019-13247-6
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Basu S, Olieric V, Leonarski F, Matsugaki N, Kawano Y, Takashi T, et al.
Long-wavelength native-SAD phasing: opportunities and challenges
IUCrJ. 2019; 6(3): 1-14. https://doi.org/10.1107/S2052252519002756
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Bliven SE, Lafita A, Rose PW, Capitani G, Prlić A, Bourne PE
Analyzing the symmetrical arrangement of structural repeats in proteins with CE-Symm
PLoS Computational Biology. 2019; 15(4): e1006842 (18 pp.). https://doi.org/10.1371/journal.pcbi.1006842
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Blum TB, Hahn A, Meier T, Davies KM, Kühlbrandt W
Dimers of mitochondrial ATP synthase induce membrane curvature and self-assemble into rows
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2019; 116(10): 4250-4255. https://doi.org/10.1073/pnas.1816556116
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Brindisi M, Ulivieri C, Alfano G, Gemma S, de Asís Balaguer F, Khan T, et al.
Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents
European Journal of Medicinal Chemistry. 2019; 162: 290-320. https://doi.org/10.1016/j.ejmech.2018.11.004
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Brunner JD, Schenck S
Preparation of proteoliposomes with purified TMEM16 protein for accurate measures of lipid scramblase activity
In: Drin G, ed. Intracellular lipid transport. Methods in molecular biology. New York, NY, USA: Humana Press; 2019:181-199. https://doi.org/10.1007/978-1-4939-9136-5_14
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Casadei CM, Nass K, Barty A, Hunter MS, Padeste C, Tsai C-J, et al.
Structure-factor amplitude reconstruction from serial femtosecond crystallography of two-dimensional membrane-protein crystals
IUCrJ. 2019; 6: 34-45. https://doi.org/10.1107/S2052252518014641
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Chalupska D, Różycki B, Humpolickova J, Faltova L, Klima M, Boura E
Phosphatidylinositol 4-kinase IIIβ (PI4KB) forms highly flexible heterocomplexes that include ACBD3, 14-3-3, and Rab11 proteins
Scientific Reports. 2019; 9(1): 567 (11 pp.). https://doi.org/10.1038/s41598-018-37158-6
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Chen X, Widmer LA, Stangier MM, Steinmetz MO, Stelling J, Barral Y
Remote control of microtubule plus-end dynamics and function from the minus-end
eLife. 2019; 8: e48627 (32 pp.). https://doi.org/10.7554/eLife.48627
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Cury NM, Mühlethaler T, Laranjeira ABA, Canevarolo RR, Zenatti PP, Lucena-Agell D, et al.
Structural basis of colchicine-site targeting acylhydrazones active against multidrug-resistant acute lymphoblastic leukemia
iScience. 2019; 21: 95-109. https://doi.org/10.1016/j.isci.2019.10.003
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Dohle W, Prota AE, Menchon G, Hamel E, Steinmetz MO, Potter BVL
Tetrahydroisoquinoline sulfamates as potent microtubule disruptors: synthesis, antiproliferative and antitubulin activity of dichlorobenzyl-based derivatives, and a Tubulin cocrystal structure.
ACS Omega. 2019; 4: 755-764. https://doi.org/10.1021/acsomega.8b02879
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Dolenc J, van Gunsteren WF, Prota AE, Steinmetz MO, Missimer JH
Conformational properties of the chemotherapeutic drug analogue Epothilone A: how to model a flexible protein ligand using scarcely available experimental data
Journal of Chemical Information and Modeling. 2019; 59(5): 2218-2230. https://doi.org/10.1021/acs.jcim.9b00171
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Ehrenberg D, Varma N, Deupi X, Koyanagi M, Terakita A, Schertler GFX, et al.
The two-photon reversible reaction of the bistable jumping spider rhodopsin-1
Biophysical Journal. 2019; 116(7): 1248-1258. https://doi.org/10.1016/j.bpj.2019.02.025
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Faltova L, Jiang K, Frey D, Wu Y, Capitani G, Prota AE, et al.
Crystal structure of a heterotetrameric katanin p60:p80 complex
Structure. 2019; 27(9): 1375-1383.e3. https://doi.org/10.1016/j.str.2019.07.002
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Gavriilidou AFM, Hunziker H, Mayer D, Vuckovic Z, Veprintsev DB, Zenobi R
Insights into the basal activity and activation mechanism of the β1 adrenergic receptor using native mass spectrometry
Journal of the American Society for Mass Spectrometry. 2019; 30(3): 529-537. https://doi.org/10.1007/s13361-018-2110-z
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Graeber E, Korkhov VM
Characterisation of the ligand binding sites in the translocator protein TSPO using the chimeric bacterial-mammalian constructs
Protein Expression and Purification. 2019; 164: 105456 (10 pp.). https://doi.org/10.1016/j.pep.2019.105456
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Guo W, Liu B, Yin Y, Kan X, Gong Q, Li Y, et al.
Licochalcone A protects the blood milk barrier integrity and relieves the inflammatory response in LPS-induced mastitis
Frontiers in Immunology. 2019; 10: 287 (14 pp.). https://doi.org/10.3389/fimmu.2019.00287
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Guo W, Liu B, Hu G, Kan X, Li Y, Gong Q, et al.
Vanillin protects the blood-milk barrier and inhibits the inflammatory response in LPS-induced mastitis in mice
Toxicology and Applied Pharmacology. 2019; 365: 9-18. https://doi.org/10.1016/j.taap.2018.12.022
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Górzny MŁ, Opara NL, Guzenko VA, Cadarso VJ, Schift H, Li XD, et al.
Microfabricated silicon chip as lipid membrane sample holder for serial protein crystallography
Micro and Nano Engineering. 2019; 3: 31-36. https://doi.org/10.1016/j.mne.2019.03.002
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Haider RS, Wilhelm F, Rizk A, Mutt E, Deupi X, Peterhans C, et al.
Arrestin-1 engineering facilitates complex stabilization with native rhodopsin
Scientific Reports. 2019; 9(1): 439 (13 pp.). https://doi.org/10.1038/s41598-018-36881-4
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Hooikaas PJ, Martin M, Mühlethaler T, Kuijntjes G-J, Peeters CAE, Katrukha EA, et al.
MAP7 family proteins regulate kinesin-1 recruitment and activation
Journal of Cell Biology. 2019; 218(4): 1298-1318. https://doi.org/10.1083/jcb.201808065
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Jaeger K, Bruenle S, Weinert T, Guba W, Muehle J, Miyazaki T, et al.
Structural basis for allosteric ligand recognition in the human CC chemokine receptor 7
Cell. 2019; 178(5): 1222-1230. https://doi.org/10.1016/j.cell.2019.07.028
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James D, Weinert T, Skopintsev P, Furrer A, Gashi D, Tanaka T, et al.
Improving high viscosity extrusion of microcrystals for time-resolved serial femtosecond crystallography at X-ray lasers
Journal of Visualized Experiments. 2019; 2019(144): e59087 (12 pp.). https://doi.org/10.3791/59087
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Kan X, Liu B, Guo W, Wei L, Lin Y, Guo Y, et al.
Myricetin relieves LPS-induced mastitis by inhibiting inflammatory response and repairing the blood-milk barrier
Journal of Cellular Physiology. 2019; 234(9): 16252-16262. https://doi.org/10.1002/jcp.28288
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Kashyap AS, Fernandez-Rodriguez L, Zhao Y, Monaco G, Trefny MP, Yoshida N, et al.
GEF-H1 signaling upon microtubule destabilization is required for dendritic cell activation and specific anti-tumor responses
Cell Reports. 2019; 28(13): 3367-3380.e1. https://doi.org/10.1016/j.celrep.2019.08.057
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La Sala G, Olieric N, Sharma A, Viti F, de Asis Balaguer Perez F, Huang L, et al.
Structure, thermodynamics, and kinetics of plinabulin binding to two tubulin isotypes
Chem. 2019; 5(11): 2969-2986. https://doi.org/10.1016/j.chempr.2019.08.022
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Liu B, Huang B, Hu G, He D, Li Y, Ran X, et al.
Isovitexin-mediated regulation of microglial polarization in lipopolysaccharide-induced neuroinflammation via activation of the CaMKKβ/AMPK-PGC-1α signaling axis
Frontiers in Immunology. 2019; 10: 2650 (17 pp.). https://doi.org/10.3389/fimmu.2019.02650
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Mayer D, Damberger FF, Samarasimhareddy M, Feldmueller M, Vuckovic Z, Flock T, et al.
Distinct G protein-coupled receptor phosphorylation motifs modulate arrestin affinity and activation and global conformation
Nature Communications. 2019; 10: 1261 (14 pp.). https://doi.org/10.1038/s41467-019-09204-y
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Montaldo NP, Bordin DL, Brambilla A, Rösinger M, Fordyce Martin SL, Bjørås KØ, et al.
Alkyladenine DNA glycosylase associates with transcription elongation to coordinate DNA repair with gene expression
Nature Communications. 2019; 10(1): 5460 (13 pp.). https://doi.org/10.1038/s41467-019-13394-w
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Munk C, Mutt E, Isberg V, Nikolajsen LF, Bibbe JM, Flock T, et al.
An online resource for GPCR structure determination and analysis
Nature Methods. 2019; 16(2): 151-162. https://doi.org/10.1038/s41592-018-0302-x
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Nagata T, Koyanagi M, Tsukamoto H, Mutt E, Schertler GFX, Deupi X, et al.
The counterion–retinylidene Schiff base interaction of an invertebrate rhodopsin rearranges upon light activation
Communications Biology. 2019; 2: 180 (9 pp.). https://doi.org/10.1038/s42003-019-0409-3
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Patterson JC, Joughin BA, Prota AE, Mühlethaler T, Jonas OH, Whitman MA, et al.
VISAGE reveals a targetable mitotic spindle vulnerability in cancer cells
Cell Systems. 2019; 9(1): 74-92.e8. https://doi.org/10.1016/j.cels.2019.05.009
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Qi C, Minin GD, Vercellino I, Wutz A, Korkhov VM
Structural basis of sterol recognition by human hedgehog receptor PTCH1
Science Advances. 2019; 5(9): eaaw6490 (9 pp.). https://doi.org/10.1126/sciadv.aaw6490
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Qi C, Sorrentino S, Medalia O, Korkhov VM
The structure of a membrane adenylyl cyclase bound to an activated stimulatory G protein
Science. 2019; 364(6438): 389-394. https://doi.org/10.1126/science.aav0778
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Samarasimhareddy M, Mayer D, Metanis N, Veprintsev D, Hurevich M, Friedler A
A targeted approach for the synthesis of multi-phosphorylated peptides: a tool for studying the role of phosphorylation patterns in proteins
Organic and Biomolecular Chemistry. 2019; 17(42): 9284-9290. https://doi.org/10.1039/c9ob01874c
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Standfuss J
Membrane protein dynamics studied by X-ray lasers - or why only time will tell
Current Opinion in Structural Biology. 2019; 57: 63-71. https://doi.org/10.1016/j.sbi.2019.02.001
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Tsai C-J, Marino J, Adaixo R, Pamula F, Muehle J, Maeda S, et al.
Cryo-EM structure of the rhodopsin-Gαi-βγ complex reveals binding of the rhodopsin C-terminal tail to the gβ subunit
eLife. 2019; 8: e46041 (19 pp.). https://doi.org/10.7554/eLife.46041
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Varma N, Mutt E, Mühle J, Panneels V, Terakita A, Deupi X, et al.
Crystal structure of jumping spider rhodopsin-1 as a light sensitive GPCR
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2019; 116(29): 14547-14556. https://doi.org/10.1073/pnas.1902192116
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Wang N, Bosc C, Ryul Choi S, Boulan B, Peris L, Olieric N, et al.
Structural basis of tubulin detyrosination by the vasohibin–SVBP enzyme complex
Nature Structural and Molecular Biology. 2019; 26(7): 571-582. https://doi.org/10.1038/s41594-019-0241-y
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Weinert T, Skopintsev P, James D, Dworkowski F, Panepucci E, Kekilli D, et al.
Proton uptake mechanism in bacteriorhodopsin captured by serial synchrotron crystallography
Science. 2019; 365(6448): 61-65. https://doi.org/10.1126/science.aaw8634
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Wickstrand C, Nogly P, Nango E, Iwata S, Standfuss J, Neutze R
Bacteriorhodopsin: structural insights revealed using X-ray lasers and synchrotron radiation
Annual Review of Biochemistry. 2019; 88: 59-83. https://doi.org/10.1146/annurev-biochem-013118-111327
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Xie Y, Mansouri M, Rizk A, Berger P
Regulation of VEGFR2 trafficking and signaling by Rab GTPase-activating proteins
Scientific Reports. 2019; 9(1): 13342 (12 pp.). https://doi.org/10.1038/s41598-019-49646-4
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Zhu X, Poghosyan E, Rezabkova L, Mehall B, Sakakibara H, Hirono M, et al.
The roles of a flagellar HSP40 ensuring rhythmic beating
Molecular Biology of the Cell. 2019; 30(2): 228-241. https://doi.org/10.1091/mbc.E18-01-0047
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de Asís Balaguer F, Mühlethaler T, Estévez-Gallego J, Calvo E, Giménez-Abián JF, Risinger AL, et al.
Crystal structure of the cyclostreptin-tubulin adduct: implications for tubulin activation by taxane-site ligands
International Journal of Molecular Sciences. 2019; 20(6): 1392 (17 pp.). https://doi.org/10.3390/ijms20061392
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Żyła DS, Prota AE, Capitani G, Glockshuber R
Alternative folding to a monomer or homopolymer is a common feature of the type 1 pilus subunit FimA from enteroinvasive bacteria
Journal of Biological Chemistry. 2019; 294(27): 10553-10563. https://doi.org/10.1074/jbc.RA119.008610
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Aher A, Kok M, Sharma A, Rai A, Olieric N, Rodriguez-Garcia R, et al.
CLASP suppresses microtubule catastrophes through a single TOG domain
Developmental Cell. 2018; 46(1): 40-58.e8. https://doi.org/10.1016/j.devcel.2018.05.032
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Ballmer-Hofer K, Hyde CAC, Schleier T, Avramovic D
ScFvs as allosteric inhibitors of VEGFR-2: novel tools to harness VEGF signaling
International Journal of Molecular Sciences. 2018; 19(5): 1334 (15 pp.). https://doi.org/10.3390/ijms19051334
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Ballmer-Hofer K
Vascular Endothelial Growth Factor, from basic research to clinical applications
International Journal of Molecular Sciences. 2018; 19(12): 3750 (5 pp.). https://doi.org/10.3390/ijms19123750
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Beazley-Long N, Moss CE, Ashby WR, Bestall SM, Almahasneh F, Durrant AM, et al.
VEGFR2 promotes central endothelial activation and the spread of pain in inflammatory arthritis
Brain, Behavior, and Immunity. 2018; 74: 49-67. https://doi.org/10.1016/j.bbi.2018.03.012
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Bianchi S, Rogala KB, Dynes NJ, Hilbert M, Leidel SA, Steinmetz MO, et al.
Interaction between the Caenorhabditis elegans centriolar protein SAS-5 and microtubules facilitates organelle assembly
Molecular Biology of the Cell. 2018; 29(6): 722-735. https://doi.org/10.1091/mbc.E17-06-0412
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Bliven S, Lafita A, Parker A, Capitani G, Duarte JM
Automated evaluation of quaternary structures from protein crystals
PLoS Computational Biology. 2018; 14(4): e1006104 (19 pp.). https://doi.org/10.1371/journal.pcbi.1006104
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Bueno O, Estévez Gallego J, Martins S, Prota AE, Gago F, Gómez-SanJuan A, et al.
High-affinity ligands of the colchicine domain in tubulin based on a structure-guided design
Scientific Reports. 2018; 8(1): 4242 (17 pp.). https://doi.org/10.1038/s41598-018-22382-x
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Casadei CM, Tsai C-J, Barty A, Hunter MS, Zatsepin NA, Padeste C, et al.
Resolution extension by image summing in serial femtosecond crystallography of two-dimensional membrane-protein crystals
IUCrJ. 2018; 5(1): 103-117. https://doi.org/10.1107/S2052252517017043
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Dohle W, Jourdan FL, Menchon G, Prota AE, Foster PA, Mannion P, et al.
Quinazolinone-based anticancer agents: synthesis, antiproliferative SAR, antitubulin activity, and tubulin Co-crystal structure
Journal of Medicinal Chemistry. 2018; 61(3): 1031-1044. https://doi.org/10.1021/acs.jmedchem.7b01474
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Field JJ, Pera B, Estévez Gallego J, Calvo E, Rodríguez-Salarichs J, Sáez-Calvo G, et al.
Zampanolide binding to tubulin indicates cross-talk of taxane site with colchicine and nucleotide sites
Journal of Natural Products. 2018; 81(3): 494-505. https://doi.org/10.1021/acs.jnatprod.7b00704
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Gavriilidou AFM, Holding FP, Mayer D, Coyle JE, Veprintsev DB, Zenobi R
Native mass spectrometry gives insight into the allosteric binding mechanism of M2 pyruvate kinase to fructose-1,6-bisphosphate
Biochemistry. 2018; 57(11): 1685-1689. https://doi.org/10.1021/acs.biochem.7b01270
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Gerrard E, Mutt E, Nagata T, Koyanagi M, Flock T, Lesca E, et al.
Convergent evolution of tertiary structure in rhodopsin visual proteins from vertebrates and box jellyfish
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2018; 115(24): 6201-6206. https://doi.org/10.1073/pnas.1721333115
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Gorobtsov OY, Mercurio G, Capotondi F, Skopintsev P, Lazarev S, Zaluzhnyy IA, et al.
Seeded X-ray free-electron laser generating radiation with laser statistical properties
Nature Communications. 2018; 9(1): 4498 (6 pp.). https://doi.org/10.1038/s41467-018-06743-8
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Graeber E, Korkhov VM
Expression and purification of the mammalian translocator protein for structural studies
PLoS One. 2018; 13(6): e0198832 (17 pp.). https://doi.org/10.1371/journal.pone.0198832
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Gruene T, Li T, van Genderen E, Pinar AB, van Bokhoven JA
Characterization at the level of individual crystals: single-crystal MFI type zeolite grains
Chemistry: A European Journal. 2018; 24(10): 2384-2388. https://doi.org/10.1002/chem.201704213
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Gruene T, Wennmacher JTC, Zaubitzer C, Holstein JJ, Heidler J, Fecteau-Lefebvre A, et al.
Rapid structure determination of microcrystalline molecular compounds using electron diffraction
Angewandte Chemie International Edition. 2018; 57(50): 16313-16317. https://doi.org/10.1002/anie.201811318
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Hajizadeh NR, Pieprzyk J, Skopintsev P, Flayhan A, Svergun DI, Löw C
Probing the architecture of a multi-PDZ domain protein: structure of PDZK1 in solution
Structure. 2018; 26(11): 1522-1533. https://doi.org/10.1016/j.str.2018.07.016
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Holler M, Raabe J, Diaz A, Guizar-Sicairos M, Wepf R, Odstrcil M, et al.
OMNY – a tOMography Nano crYo stage
Review of Scientific Instruments. 2018; 89(4): 043706 (13 pp.). https://doi.org/10.1063/1.5020247
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Huang C-Y, Olieric V, Howe N, Warshamanage R, Weinert T, Panepucci E, et al.
In situ serial crystallography for rapid de novo membrane protein structure determination.
Communications Biology. 2018; 1: 124 (8 pp.). https://doi.org/10.1038/S42003-018-0123-6
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Ishikawa T
Organization of dyneins in the axoneme
In: King SM, ed. Dyneins: The biology of dynein motors. Amsterdam: Elsevier; 2018:203-217. https://doi.org/10.1016/B978-0-12-809471-6.00006-1
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Jiang K, Faltova L, Hua S, Capitani G, Prota AE, Landgraf C, et al.
Structural basis of formation of the microtubule minus-end-regulating CAMSAP-katanin complex
Structure. 2018; 26(3): 375-382. https://doi.org/10.1016/j.str.2017.12.017
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Kraatz SHW, Bianchi S, Steinmetz MO
Combinatorial use of disulfide bridges and native sulfur-SAD phasing for rapid structure determination of coiled-coils
Bioscience Reports. 2018; 38(5): BSR20181073 (11 pp.). https://doi.org/10.1042/BSR20181073
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Lafita A, Bliven S, Kryshtafovych A, Bertoni M, Monastyrskyy B, Duarte JM, et al.
Assessment of protein assembly prediction in CASP12
Proteins. 2018; 86(S1): 247-256. https://doi.org/10.1002/prot.25408
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Lampert F, Stafa D, Goga A, Soste MV, Gilberto S, Olieric N, et al.
The multi-subunit GID/CTLH e3 ubiquitin ligase promotes cell proliferation and targets the transcription factor Hbp1 for degradation
eLife. 2018; 7: e35528 (23 pp.). https://doi.org/10.7554/eLife.35528
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Lesca E, Panneels V, Schertler GFX
The role of water molecules in phototransduction of retinal proteins and G protein-coupled receptors
Faraday Discussions. 2018; 207: 27-37. https://doi.org/10.1039/c7fd00207f
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Liu T, Ish-Shalom S, Torng W, Lafita A, Bock C, Mort M, et al.
Biological and functional relevance of CASP predictions
Proteins. 2018; 86(1): 374-386. https://doi.org/10.1002/prot.25396
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Mansouri M, Berger P
Baculovirus for gene delivery to mammalian cells: past, present and future
Plasmid. 2018; 98: 1-7. https://doi.org/10.1016/j.plasmid.2018.05.002
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Mansouri M, Berger P
Multigene delivery in mammalian cells: recent advances and applications
Biotechnology Advances. 2018; 36(4): 871-879. https://doi.org/10.1016/j.biotechadv.2018.01.012
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Mattle D, Kuhn B, Aebi J, Bedoucha M, Kekilli D, Grozinger N, et al.
Ligand channel in pharmacologically stabilized rhodopsin
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2018; 115(14): 3640-3645. https://doi.org/10.1073/pnas.1718084115
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Menchon G, Prota AE, Lucena-Agell D, Bucher P, Jansen R, Irschik H, et al.
A fluorescence anisotropy assay to discover and characterize ligands targeting the maytansine site of tubulin
Nature Communications. 2018; 9(1): 2106 (9 pp.). https://doi.org/10.1038/s41467-018-04535-8
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Menchon G, Maveyraud L, Czaplicki G
Molecular dynamics as a tool for virtual ligand screening
In: Gore M, Jagtap UB, eds. Computational drug discovery and design. Methods in molecular biology. New York: Humana Press; 2018:145-178. https://doi.org/10.1007/978-1-4939-7756-7_9
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Narwal M, Jemth AS, Gustafsson R, Almlöf I, Warpman Berglund U, Helleday T, et al.
Crystal structures and inhibitor interactions of mouse and dog MTH1 reveal species-specific differences in affinity
Biochemistry. 2018; 57(5): 593-603. https://doi.org/10.1021/acs.biochem.7b01163
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Nogly P, Weinert T, James D, Carbajo S, Ozerov D, Furrer A, et al.
Retinal isomerization in bacteriorhodopsin captured by a femtosecond x-ray laser
Science. 2018; 361(6398): eaat0094 (7 pp.). https://doi.org/10.1126/science.aat0094
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Preobraschenski J, Cheret C, Ganzella M, Zander JF, Richter K, Schenck S, et al.
Dual and direction-selective mechanisms of phosphate transport by the vesicular glutamate transporter
Cell Reports. 2018; 23(2): 535-545. https://doi.org/10.1016/j.celrep.2018.03.055
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Rose M, Senkbeil T, von Gundlach AR, Stuhr S, Rumancev C, Dzhigaev D, et al.
Quantitative ptychographic bio-imaging in the water window
Optics Express. 2018; 26(2): 1237-1254. https://doi.org/10.1364/OE.26.001237
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Sharma A, Gerard SF, Olieric N, Steinmetz MO
Cep120 promotes microtubule formation through a unique tubulin binding C2 domain
Journal of Structural Biology. 2018; 203(1): 62-70. https://doi.org/10.1016/j.jsb.2018.01.009
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Smedley CJ, Stanley PA, Qazzaz ME, Prota AE, Olieric N, Collins H, et al.
Sustainable syntheses of (-)-jerantinines A & E and structural characterisation of the jerantinine-tubulin complex at the colchicine binding site
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Schmidt F, Treiber N, Zocher G, Bjelic S, Steinmetz MO, Kalbacher H, et al.
Insights into peroxisome function from the structure of PEX3 in complex with a soluble fragment of PEX19
Journal of Biological Chemistry. 2010; 285(33): 25410-25417. https://doi.org/10.1074/jbc.M110.138503
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Schärer MA, Grütter MG, Capitani G
CRK: an evolutionary approach for distinguishing biologically relevant interfaces from crystal contacts
Proteins. 2010; 78(12): 2707-2713. https://doi.org/10.1002/prot.22787
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Stehr H, Duarte JM, Lappe M, Bhak J, Bolser DM
PDBWiki: added value through community annotation of the Protein Data Bank
Database: The Journal of Biological Databases and Curation. 2010; 2010: baq009 (8 pp.). https://doi.org/10.1093/database/baq009
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Truan D, Huergo LF, Chubatsu LS, Merrick M, Li X-D, Winkler FK
A new PII protein structure identifies the 2-oxoglutarate binding site
Journal of Molecular Biology. 2010; 400(3): 531-539. https://doi.org/10.1016/j.jmb.2010.05.036
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Balsera M, Goetze TA, Kovács-Bogdán E, Schürmann P, Wagner R, Buchanan BB, et al.
Characterization of Tic110, a channel-forming protein at the inner envelope membrane of chloroplasts, unveils a response to Ca2+ and a stromal regulatory disulfide bridge
Journal of Biological Chemistry. 2009; 284(5): 2603-2616. https://doi.org/10.1074/jbc.M807134200
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Balsera M, Soll J, Buchanan BB
Protein import in chloroplasts: an emerging regulatory role for redox
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Balsera M, Soll J, Bölter B
Protein import machineries in endosymbiotic organelles
Cellular and Molecular Life Sciences. 2009; 66(11-12): 1903-1923. https://doi.org/10.1007/s00018-009-8644-2
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Bieniossek C, Nie Y, Frey D, Olieric N, Schaffitzel C, Collinson I, et al.
Automated unrestricted multigene recombineering for multiprotein complex production
Nature Methods. 2009; 6(6): 447-450. https://doi.org/10.1038/nmeth.1326
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Friedli A, Fischer E, Novak-Hofer I, Cohrs S, Ballmer-Hofer K, Schubiger PA, et al.
The soluble form of the cancer-associated L1 cell adhesion molecule is a pro-angiogenic factor
International Journal of Biochemistry and Cell Biology. 2009; 41(7): 1572-1580. https://doi.org/10.1016/j.biocel.2009.01.006
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Gut H, Dominici P, Pilati S, Astegno A, Petoukhov MV, Svergun DI, et al.
A common structural basis for pH- and calmodulin-mediated regulation in plant glutamate decarboxylase
Journal of Molecular Biology. 2009; 392(2): 334-351. https://doi.org/10.1016/j.jmb.2009.06.080
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Honnappa S, Gouveia SM, Weisbrich A, Damberger FF, Bhavesh NS, Jawhari H, et al.
An EB1-binding motif acts as a microtubule tip localization signal
Cell. 2009; 138(2): 366-376. https://doi.org/10.1016/j.cell.2009.04.065
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Komarova Y, De Groot CO, Grigoriev I, Gouveia SM, Munteanu EL, Schober JM, et al.
Mammalian end binding proteins control persistent microtubule growth
Journal of Cell Biology. 2009; 184(5): 691-706. https://doi.org/10.1083/jcb.200807179
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Li X-D, Huergo LF, Gasperina A, Pedrosa FO, Merrick M, Winkler FK
Crystal Structure of Dinitrogenase Reductase-activating Glycohydrolase (DRAG) Reveals Conservation in the ADP-Ribosylhydrolase Fold and Specific Features in the ADP-Ribose-binding Pocket
Journal of Molecular Biology. 2009; 390(4): 737-746. https://doi.org/10.1016/j.jmb.2009.05.031
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Lingaraju GM, Prota AE, Winkler FK
Mutational studies of Pa-AGOG DNA glycosylase from the hyperthermophilic crenarchaeon Pyrobaculum aerophilum
DNA Repair. 2009; 8(7): 857-864. https://doi.org/10.1016/j.dnarep.2009.03.009
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Manna T, Thrower DA, Honnappa S, Steinmetz MO, Wilson L
Regulation of microtubule dynamic instability in vitro by differentially phosphorylated stathmin
Journal of Biological Chemistry. 2009; 284(23): 15640-15649. https://doi.org/10.1074/jbc.M900343200
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Palfi Z, Jaé N, Preußer C, Kaminska KH, Bujnicki JM, Lee JH, et al.
SMN-assisted assembly of snRNP-specific Sm cores in trypanosomes
Genes and Development. 2009; 23(14): 1650-1664. https://doi.org/10.1101/gad.526109
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Pennacchietti E, Lammens TM, Capitani G, Franssen MCR, John RA, Bossa F, et al.
Mutation of His465 alters the pH-dependent spectroscopic properties of Escherichia coli glutamate decarboxylase and broadens the range of its activity toward more alkaline pH
Journal of Biological Chemistry. 2009; 284(46): 31587-31596. https://doi.org/10.1074/jbc.M109.049577
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Studer A, Han X, Winkler FK, Tiefenauer LX
Formation of individual protein channels in lipid bilayers suspended in nanopores
Colloids and Surfaces B: Biointerfaces. 2009; 73(2): 325-331. https://doi.org/10.1016/j.colsurfb.2009.06.006
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Stuttfeld E, Ballmer-Hofer K
Structure and function of VEGF receptors
IUBMB Life. 2009; 61(9): 915-922. https://doi.org/10.1002/iub.234
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Tremmel M, Matzke A, Albrecht I, Laib AM, Olaku V, Ballmer-Hofer K, et al.
A CD44v6 peptide reveals a role of CD44 in VEGFR-2 signaling and angiogenesis
Blood. 2009; 114(25): 5236-5244. https://doi.org/10.1182/blood-2009-04-219204
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Wasmer C, Benkemoun L, Sabaté R, Steinmetz MO, Coulary-Salin B, Wang L, et al.
Solid-state NMR spectroscopy reveals that E. coli inclusion bodies of HET-s(218-289) are amyloids
Angewandte Chemie International Edition. 2009; 48(26): 4858-4860. https://doi.org/10.1002/anie.200806100
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Patterson BD, Heyderman L, Milne C, Thibault P, Ballmer K, Staub U, eds.
Ultrafast phenomena at the nanoscale: science opportunities at the SwissFEL X-ray laser
Villigen PSI, Switzerland: Paul Scherrer Institut; 2009.
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Akhmanova A, Steinmetz MO
Tracking the ends: a dynamic protein network controls the fate of microtubule tips
Nature Reviews Molecular Cell Biology. 2008; 9(4): 309-322. https://doi.org/10.1038/nrm2369
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Azzaroni O, Mir M, Álvarez M, Tiefenauer L, Knoll W
Electrochemical rectification by redox-labeled bioconjugates: molecular building blocks for the construction of biodiodes
Langmuir. 2008; 24(6): 2878-2883. https://doi.org/10.1021/la703536a
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Cébe-Suarez S, Grünewald FS, Jaussi R, Li X, Claesson-Welsh L, Spillmann D, et al.
Orf virus VEGF-E NZ2 promotes paracellular NRP-1/VEGFR-2 coreceptor assembly via the peptide RPPR
FASEB Journal. 2008; 22(8): 3078-3086. https://doi.org/10.1096/fj.08-107219
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Dais C, Solak HH, Müller E, Grützmacher D
Impact of template variations on shape and arrangement of Si/Ge quantum dot arrays
Applied Physics Letters. 2008; 92(14): 143102 (3 pp.). https://doi.org/10.1063/1.2907196
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Dolenc J, Baron R, Missimer JH, Steinmetz MO, van Gunsteren WF
Exploring the conserved water site and hydration of a coiled-coil trimerisation motif: a MD simulation study
ChemBioChem. 2008; 9(11): 1749-1756. https://doi.org/10.1002/cbic.200800096
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Grigoriev I, Gouveia SM, van der Vaart B, Demmers J, Smyth JT, Honnappa S, et al.
STIM1 is a MT-plus-end-tracking protein involved in remodeling of the ER
Current Biology. 2008; 18(3): 177-182. https://doi.org/10.1016/j.cub.2007.12.050
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Grimshaw JPA, Stirnimann CU, Brozzo MS, Malojcic G, Grütter MG, Capitani G, et al.
DsbL and DsbI form a specific dithiol oxidase system for periplasmic arylsulfate sulfotransferase in uropathogenic Escherichia coli
Journal of Molecular Biology. 2008; 380(4): 667-680. https://doi.org/10.1016/j.jmb.2008.05.031
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Hartmann S, Missimer JH, Stoeckel C, Abela E, Shah J, Seitz RJ, et al.
Functional connectivity in tactile object discrimination - a principal component analysis of an event related fMRI-study
PLoS One. 2008; 3(12): e3831 (13 pp.). https://doi.org/10.1371/journal.pone.0003831
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Hwang S-J, Kim SH, Kim H-Z, Steinmetz MO, Koh GY, Lee GM
High-level expression and purification of a designed angiopoietin-1 chimeric protein, COMP-Ang1, produced in Chinese hamster ovary cells
Protein Journal. 2008; 27(5): 319-326. https://doi.org/10.1007/s10930-008-9140-5
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Javelle A, Lupo D, Ripoche P, Fulford T, Merrick M, Winkler FK
Substrate binding, deprotonation, and selectivity at the periplasmic entrance of the Escherichia coli ammonia channel AmtB
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2008; 105(13): 5040-5045. https://doi.org/10.1073/pnas.0711742105
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Kawamura H, Li X, Goishi K, van Meeteren LA, Jakobsson L, Cébe-Suarez S, et al.
Neuropilin-1 in regulation of VEGF-induced activation of p38MAPK and endothelial cell organization
Blood. 2008; 112(9): 3638-3649. https://doi.org/10.1182/blood-2007-12-125856
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Licht K, Medenbach J, Lührmann R, Kambach C, Bindereif A
3'-cyclic phosphorylation of U6 snRNA leads to recruitment of recycling factor p110 through LSm proteins
RNA. 2008; 14(8): 1532-1538. https://doi.org/10.1261/rna.1129608
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Manna T, Honnappa S, Steinmetz MO, Wilson L
Suppression of microtubule dynamic instability by the +TIP protein EB1 and its modulation by the CAP-Gly domain of p150Glued
Biochemistry. 2008; 47(2): 779-786. https://doi.org/10.1021/bi701912g
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Mir M, Álvarez M, Azzaroni O, Tiefenauer L, Knoll W
Molecular architectures for electrocatalytic amplification of oligonucleotide hybridization
Analytical Chemistry. 2008; 80(17): 6554-6559. https://doi.org/10.1021/ac800560t
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Narzi D, Siu SWI, Stirnimann CU, Grimshaw JPA, Glockshuber R, Capitani G, et al.
Evidence for proton shuffling in a thioredoxin-like protein during catalysis
Journal of Molecular Biology. 2008; 382(4): 978-986. https://doi.org/10.1016/j.jmb.2008.07.061
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Nomi JS, Scherfeld D, Friederichs S, Schäfer R, Franz M, Wittsack H-J, et al.
On the neural networks of empathy: a principal component analysis of an fMRI study
Behavioral and Brain Functions. 2008; 4: 41 (13 pp.). https://doi.org/10.1186/1744-9081-4-41
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Puorger C, Eidam O, Capitani G, Erilov D, Grütter MG, Glockshuber R
Infinite kinetic stability against dissociation of supramolecular protein complexes through donor strand complementation
Structure. 2008; 16(4): 631-642. https://doi.org/10.1016/j.str.2008.01.013
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Rennel ES, Hamdollah-Zadeh MA, Wheatley ER, Magnussen A, Schüler Y, Kelly SP, et al.
Recombinant human VEGF165b protein is an effective anti-cancer agent in mice
European Journal of Cancer. 2008; 44(13): 1883-1894. https://doi.org/10.1016/j.ejca.2008.05.027
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Soro S, Orecchia A, Morbidelli L, Lacal PM, Morea V, Ballmer-Hofer K, et al.
A proangiogenic peptide derived from vascular endothelial growth factor receptor-1 acts through α5β1 integrin
Blood. 2008; 111(7): 3479-3488. https://doi.org/10.1182/blood-2007-03-077537
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Steinmetz MO, Gattin Z, Verel R, Ciani B, Stromer T, Green JM, et al.
Atomic models of de novo designed ccβ-Met amyloid-like fibrils
Journal of Molecular Biology. 2008; 376(3): 898-912. https://doi.org/10.1016/j.jmb.2007.11.100
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Steinmetz MO, Akhmanova A
Capturing protein tails by CAP-Gly domains
Trends in Biochemical Sciences. 2008; 33(11): 535-545. https://doi.org/10.1016/j.tibs.2008.08.006
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Tiefenauer LX, Studer A
Nano for bio: nanopore arrays for stable and functional lipid bilayer membranes
Biointerphases: A Journal of Biomaterials and Biological Interfaces. 2008; 3(2): FA75-FA79. https://doi.org/10.1116/1.2912932
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Vacca RA, Giannattasio S, Capitani G, Marra E, Christen P
Molecular evolution of B6 enzymes: binding of pyridoxal-5'-phosphate and Lys41Arg substitution turn ribonuclease A into a model B6 protoenzyme
BMC Biochemistry. 2008; 9(1): 17 (10 pp.). https://doi.org/10.1186/1471-2091-9-17
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Verel R, Tomka IT, Bertozzi C, Cadalbert R, Kammerer RA, Steinmetz MO, et al.
Polymorphism in an amyloid-like fibril-forming model peptide
Angewandte Chemie International Edition. 2008; 47(31): 5842-5845. https://doi.org/10.1002/anie.200800021
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Zaric BL, Kambach C
Reconstitution of recombinant human LSm complexes for biochemical, biophysical, and cell biological studies
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Baatout S, Jaussi R, Michaux A, Buset J, Schoonjans W, Jacquet P
Intracellular signal transduction in mouse oocytes and irradiated early embryos
In Vivo. 2007; 21(4): 587-592.
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Bergman N, Moraes KCM, Anderson JR, Zaric B, Kambach C, Schneider RJ, et al.
Lsm proteins bind and stabilize RNAs containing 5′ poly(A) tracts
Nature Structural and Molecular Biology. 2007; 14(9): 824-831. https://doi.org/10.1038/nsmb1287
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Conroy MJ, Durand A, Lupo D, Li X-D, Bullough PA, Winkler FK, et al.
The crystal structure of the Escherichia coli AmtB-GlnK complex reveals how GlnK regulates the ammonia channel
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2007; 104(4): 1213-1218. https://doi.org/10.1073/pnas.0610348104
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Dais C, Solak HH, Ekinci Y, Müller E, Sigg H, Grützmacher D
Ge quantum dot molecules and crystals: preparation and properties
Surface Science. 2007; 601(13): 2787-2791. https://doi.org/10.1016/j.susc.2006.12.053
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Fitzgerald DJ, Schaffitzel C, Berger P, Wellinger R, Bieniossek C, Richmond TJ, et al.
Multiprotein expression strategy for structural biology of eukaryotic complexes
Structure. 2007; 15(3): 275-279. https://doi.org/10.1016/j.str.2007.01.016
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Frey D, Kambach C, Steinmetz MO, Jaussi R
Production of in vitro amplified DNA pseudolibraries and high-throughput cDNA target amplification
BMC Biotechnology. 2007; 7: 31 (5 pp.). https://doi.org/10.1186/1472-6750-7-31
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Grützmacher D, Dais C, Zhang L, Müller E, Solak HH
Templated self-organization of SiGe quantum structures for nanoelectronics
Materials Science and Engineering C: Biomimetic Materials, Sensors and Systems. 2007; 27(5-8): 947-953. https://doi.org/10.1016/j.msec.2006.07.029
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Grützmacher D, Fromherz T, Dais C, Stangl J, Müller E, Ekinci Y, et al.
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Nanopore arrays for stable and functional free-standing lipid bilayers
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Javelle A, Lupo D, Li X-D, Merrick M, Chami M, Ripoche P, et al.
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Javelle A, Lupo D, Li X-D, Merrick M, Chami M, Ripoche P, et al.
Structural and mechanistic aspects of Amt/Rh proteins
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John CM, Hite RK, Weirich CS, Fitzgerald DJ, Jawhari H, Faty M, et al.
The Caenorhabditis elegans septin complex is nonpolar
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Kambach C
Pipelines, robots, crystals and biology: what use high throughput solving structures of challenging targets?
Current Protein and Peptide Science. 2007; 8(2): 205-217. https://doi.org/10.2174/138920307780363442
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Koller-Eichhorn R, Marquardt T, Gail R, Wittinghofer A, Kostrewa D, Kutay U, et al.
Human OLA1 defines an ATPase subfamily in the Obg family of GTP-binding proteins
Journal of Biological Chemistry. 2007; 282(27): 19928-19937. https://doi.org/10.1074/jbc.M700541200
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Lupo D, Li X-D, Durand A, Tomizaki T, Cherif-Zahar B, Matassi G, et al.
The 1.3-Å resolution structure of Nitrosomonas europaea Rh50 and mechanistic implications for NH3 transport by Rhesus family proteins
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2007; 104(49): 19303-19308. https://doi.org/10.1073/pnas.0706563104
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Missimer JH, Steinmetz MO, Baron R, Winkler FK, Kammerer RA, Daura X, et al.
Configurational entropy elucidates the role of salt-bridge networks in protein thermostability
Protein Science. 2007; 16(7): 1349-1359. https://doi.org/10.1110/ps.062542907
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Ruch C, Skiniotis G, Steinmetz MO, Walz T, Ballmer-Hofer K
Structure of a VEGF–VEGF receptor complex determined by electron microscopy
Nature Structural and Molecular Biology. 2007; 14(3): 249-250. https://doi.org/10.1038/nsmb1202
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Scherr N, Honnappa S, Kunz G, Mueller P, Jayachandran R, Winkler F, et al.
Structural basis for the specific inhibition of protein kinase G, a virulence factor of Mycobacterium tuberculosis
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2007; 104(29): 12151-12156. https://doi.org/10.1073/pnas.0702842104
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Severi E, Javelle A, Merrick M
The conserved carboxy-terminal region of the ammonia channel AmtB plays a critical role in channel function
Molecular Membrane Biology. 2007; 24(2): 161-171. https://doi.org/10.1080/09687860601129420
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Steinmetz MO, Jelesarov I, Matousek WM, Honnappa S, Jahnke W, Missimer JH, et al.
Molecular basis of coiled-coil formation
Proceedings of the National Academy of Sciences of the United States of America PNAS. 2007; 104(17): 7062-7067. https://doi.org/10.1073/pnas.0700321104
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Steinmetz MO
Structure and thermodynamics of the tubulin–stathmin interaction
Journal of Structural Biology. 2007; 158(2): 137-147. https://doi.org/10.1016/j.jsb.2006.07.018
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Studer R, Dahinden P, Wang W-W, Auchli Y, Li X-D, Dimroth P
Crystal structure of the carboxyltransferase domain of the oxaloacetate decarboxylase Na+ pump from Vibrio cholerae
Journal of Molecular Biology. 2007; 367(2): 547-557. https://doi.org/10.1016/j.jmb.2006.12.035
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Tersar K, Boentert M, Berger P, Bonneick S, Wessig C, Toyka KV, et al.
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2
Human Molecular Genetics. 2007; 16(24): 2991-3001. https://doi.org/10.1093/hmg/ddm257
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Teuling E, Ahmed S, Haasdijk E, Demmers J, Steinmetz MO, Akhmanova A, et al.
Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates
Journal of Neuroscience. 2007; 27(36): 9801-9815. https://doi.org/10.1523/JNEUROSCI.2661-07.2007
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Weisbrich A, Honnappa S, Jaussi R, Okhrimenko O, Frey D, Jelesarov I, et al.
Structure-function relationship of CAP-Gly domains
Nature Structural and Molecular Biology. 2007; 14(10): 959-967. https://doi.org/10.1038/nsmb1291
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Zehnder-Fjällman AHM, Marty C, Halin C, Hohn A, Schibli R, Ballmer-Hofer K, et al.
Evaluation of anti-VEGFR-3 specific scFv antibodies as potential therapeutic and diagnostic tools for tumor lymph-angiogenesis
Oncology Reports. 2007; 18(4): 933-941. https://doi.org/10.3892/or.18.4.933
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Brem F, Tiefenauer L, Fink A, Dobson J, Hirt AM
A mixture of ferritin and magnetite nanoparticles mimics the magnetic properties of human brain tissue
Physical Review B. 2006; 73(22): 224427 (6 pp.). https://doi.org/10.1103/PhysRevB.73.224427
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Cébe Suarez S, Pieren M, Cariolato L, Arn S, Hoffmann U, Bogucki A, et al.
A VEGF-A splice variant defective for heparan sulfate and neuropilin-1 binding shows attenuated signaling through VEGFR-2
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Cébe-Suarez S, Zehnder-Fjällman A, Ballmer-Hofer K
The role of VEGF receptors in angiogenesis; complex partnerships
Cellular and Molecular Life Sciences. 2006; 63(5): 601-615. https://doi.org/10.1007/s00018-005-5426-3
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Fitzgerald DJ, Berger P, Schaffitzel C, Yamada K, Richmond TJ, Berger I
Protein complex expression by using multigene baculoviral vectors
Nature Methods. 2006; 3(12): 1021-1032. https://doi.org/10.1038/nmeth983
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Honnappa S, Jahnke W, Seelig J, Steinmetz MO
Control of intrinsically disordered stathmin by multisite phosphorylation
Journal of Biological Chemistry. 2006; 281(23): 16078-16083. https://doi.org/10.1074/jbc.M513524200
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Honnappa S, Okhrimenko O, Jaussi R, Jawhari H, Jelesarov I, Winkler FK, et al.
Key interaction modes of dynamic +TIP networks
Molecular Cell. 2006; 23(5): 663-671. https://doi.org/10.1016/j.molcel.2006.07.013
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Javelle A, Lupo D, Zheng L, Li X-D, Winkler FK, Merrick M
An unusual twin-His arrangement in the pore of ammonia channels is essential for substrate conductance
Journal of Biological Chemistry. 2006; 281(51): 39492-39498. https://doi.org/10.1074/jbc.M608325200
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Kammerer RA, Steinmetz MO
De novo design of a two-stranded coiled-coil switch peptide
Journal of Structural Biology. 2006; 155(2): 146-153. https://doi.org/10.1016/j.jsb.2006.01.017
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Li XD, Lupo D, Zheng L, Winkler F
Structural and functional insights into the AmtB/Mep/Rh protein family
Transfusion Clinique et Biologique. 2006; 13(1-2): 65-69. https://doi.org/10.1016/j.tracli.2006.02.014
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Liu J, Tiefenauer L, Tian S, Nielsen PE, Knoll W
PNA-DNA hybridization study using labeled streptavidin by voltammetry and surface plasmon fluorescence spectroscopy
Analytical Chemistry. 2006; 78(2): 470-476. https://doi.org/10.1021/ac051299c
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Macdonald PR, Progias P, Ciani B, Patel S, Mayer U, Steinmetz MO, et al.
Structure of the extracellular domain of tie receptor tyrosine kinases and localization of the angiopoietin-binding epitope
Journal of Biological Chemistry. 2006; 281(38): 28408-28414. https://doi.org/10.1074/jbc.M605219200
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Marty C, Langer-Machova Z, Sigrist S, Schott H, Schwendener RA, Ballmer-Hofer K
Isolation and characterization of a scFv antibody specific for tumor endothelial marker 1 (TEM1), a new reagent for targeted tumor therapy
Cancer Letters. 2006; 235(2): 298-308. https://doi.org/10.1016/j.canlet.2005.04.029
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