¹⁹F NMR as a tool in chemical biology

Scholarly Works

• Stockman, B. J.; Ventura, C. A.; Deykina, V. S.; Khayan Lontscharitsch, N.; Saljanin, E.; Gil, A.; Canestrari, M.; Mahmood, M. Direct Measurement of Nucleoside Ribohydrolase Enzyme Activities in Trichomonas vaginalis Cells Using 19F and 13C-Edited 1H NMR Spectroscopy. Analytical chemistry 2023, 95, 5300–5306. doi:10.1021/acs.analchem.2c05330
• Elena-Real, C. A.; Sagar, A.; Urbanek, A.; Popovic, M.; Morató, A.; Estaña, A.; Fournet, A.; Doucet, C.; Lund, X. L.; Shi, Z.-D.; Costa, L.; Thureau, A.; Allemand, F.; Swenson, R. E.; Milhiet, P.-E.; Crehuet, R.; Barducci, A.; Cortés, J.; Sinnaeve, D.; Sibille, N.; Bernadó, P. The structure of pathogenic huntingtin exon 1 defines the bases of its aggregation propensity. Nature structural & molecular biology 2023, 30, 309–320. doi:10.1038/s41594-023-00920-0
• Audsley, G.; Carpenter, H.; Essien, N. B.; Lai-Morrice, J.; Al-Hilaly, Y.; Serpell, L. C.; Akien, G. R.; Tizzard, G. J.; Coles, S. J.; Ulldemolins, C. P.; Kostakis, G. E. Chiral Co3Y Propeller-Shaped Chemosensory Platforms Based on 19F-NMR. Inorganic chemistry 2023, 62, 2680–2693. doi:10.1021/acs.inorgchem.2c03737
• Sales, T. A.; Gonçalves, M. A.; Ramalho, T. C. Structural Parameters of the Interaction between Ciprofloxacin and Human Topoisomerase-II β Enzyme: Toward New 19F NMR Chemical Shift Probes. Magnetochemistry 2022, 8, 181. doi:10.3390/magnetochemistry8120181
• Silva Terra, A. I.; Rossetto, M.; Dickson, C. L.; Peat, G.; Uhrín, D.; Halse, M. E. Enhancing 19F Benchtop NMR Spectroscopy by Combining para-Hydrogen Hyperpolarization and Multiplet Refocusing. ACS measurement science au 2022, 3, 73–81. doi:10.1021/acsmeasuresciau.2c00055
• Lu, Y.; Sun, M.; Xi, N. Effects of fluorine bonding and nonbonding interactions on 19F chemical shifts. RSC advances 2022, 12, 32082–32096. doi:10.1039/d2ra06660b
• Elena-Real, C. A.; Sagar, A.; Urbanek, A.; Popovic, M.; Morató, A.; Estaña, A.; Fournet, A.; Lund, X. L.; Shi, Z.-D.; Costa, L.; Thureau, A.; Allemand, F.; Swenson, R. E.; Milhiet, P.-E.; Barducci, A.; Cortés, J.; Sinnaeve, D.; Sibille, N.; Bernadó, P. The structure of pathogenic huntingtin exon-1 defines the bases of its aggregation propensity. Cold Spring Harbor Laboratory 2022. doi:10.1101/2022.10.25.513661
• Thalhammer, A.; Bröker, N. K. Biophysical Approaches for the Characterization of Protein-Metabolite Interactions. Methods in molecular biology (Clifton, N.J.) 2022, 2554, 199–229. doi:10.1007/978-1-0716-2624-5_13
• Huang, B.; Xu, L.; Ying, J.; Zhao, Y.; Huang, S. A novel in-situ strategy for enantiomeric discrimination and selective identification of multicomponent carboxylic acids in foods. Analytica chimica acta 2022, 1230, 340402. doi:10.1016/j.aca.2022.340402
• Meng, B.; Grage, S. L.; Babii, O.; Takamiya, M.; MacKinnon, N.; Schober, T.; Hutskalov, I.; Nassar, O.; Afonin, S.; Koniev, S.; Komarov, I. V.; Korvink, J. G.; Strähle, U.; Ulrich, A. S. Highly Fluorinated Peptide Probes with Enhanced In Vivo Stability for 19 F-MRI. Small (Weinheim an der Bergstrasse, Germany) 2022, 18, e2107308–2107308. doi:10.1002/smll.202107308
• Brigaud, T.; Crousse, B.; Lequeux, T. Perfluoroalkylated Biomolecules for Medicinal Chemistry and Biological Studies. Perfluoroalkyl Substances; The Royal Society of Chemistry, 2022; pp 459–476. doi:10.1039/9781839167591-00459
• Borgini, M.; Wipf, P. Stereoselective synthesis of δ-fluorinated isoleucines exploiting consecutive C(sp3)-H bond activations. Tetrahedron 2022, 120, 132876. doi:10.1016/j.tet.2022.132876
• Wu, Q.; Liu, X.; Chai, Z.; Cheng, K.; Xu, G.; Jiang, L.; Liu, M.; Li, C. Lanmodulin remains unfolded and fails to interact with lanthanide ions in Escherichia coli cells. Chemical communications (Cambridge, England) 2022, 58, 8230–8233. doi:10.1039/d2cc02038f
• Shet, H.; Sahu, R.; Sanghvi, Y. S.; Kapdi, A. R. Strategies for the Synthesis of Fluorinated Nucleosides, Nucleotides and Oligonucleotides. Chemical record (New York, N.Y.) 2022, 22, e202200066. doi:10.1002/tcr.202200066
• Xu, Z.; Gu, S.; Li, Y.; Wu, J.; Zhao, Y. Recognition-Enabled Automated Analyte Identification via 19F NMR. Analytical chemistry 2022, 94, 8285–8292. doi:10.1021/acs.analchem.2c00642
• Landrieu, I.; Dupré, E.; Sinnaeve, D.; El Hajjar, L.; Smet-Nocca, C. Deciphering the Structure and Formation of Amyloids in Neurodegenerative Diseases With Chemical Biology Tools. Frontiers in chemistry 2022, 10, 886382. doi:10.3389/fchem.2022.886382
• Maleckis, A.; Abdelkader, E. H.; Herath, I. D.; Otting, G. Synthesis of fluorinated leucines, valines and alanines for use in protein NMR. Organic & biomolecular chemistry 2022, 20, 2424–2432. doi:10.1039/d2ob00145d
• Asanbaeva, N. B.; Sukhanov, A. A.; Diveikina, A. A.; Rogozhnikova, O. Y.; Trukhin, D. V.; Tormyshev, V. M.; Chubarov, A. S.; Maryasov, A. G.; Genaev, A. M.; Shernyukov, A. V.; Salnikov, G. E.; Lomzov, A. A.; Pyshnyi, D. V.; Bagryanskaya, E. G. Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label. Physical chemistry chemical physics : PCCP 2022, 24, 5982–6001. doi:10.1039/d1cp05445g
• Bodero, L.; Guitot, K.; Lensen, N.; Lequin, O.; Brigaud, T.; Ongeri, S.; Chaume, G. Introducing the Chiral Constrained α-Trifluoromethylalanine in Aib Foldamers to Control, Quantify and Assign the Helical Screw-Sense. Chemistry (Weinheim an der Bergstrasse, Germany) 2022, 28, e202103887. doi:10.1002/chem.202103887
• Belakhov, V. V.; Boikova, I. V.; Krasnobaeva, I. L.; Kolodyaznaya, V. A. Preparation and Insecticidal Activity of the First Organofluorine Insecticide Based on β-D-Ribofuranoside Monosaccharide. Russian Journal of General Chemistry 2021, 91, 2900–2907. doi:10.1134/s1070363221130181

Explore citations to this article at