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2019 Journal Article Periplasmic expression of 4/7 alpha-conotoxin TxIA analogs in E. coli favors ribbon isomer formation suggestion of a binding mode at the α7 nAChREl Hamdaoui, Yamina, Wu, Xiaosa, Clark, Richard J., Giribaldi, Julien, Anangi, Raveendra, Craik, David J., King, Glenn F., Dutertre, Sebastien, Kaas, Quentin, Herzig, Volker and Nicke, Annette (2019). Periplasmic expression of 4/7 alpha-conotoxin TxIA analogs in E. coli favors ribbon isomer formation suggestion of a binding mode at the α7 nAChR. Frontiers in Pharmacology, 10 (MAY) 577, 577. doi: 10.3389/fphar.2019.00577 |
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2019 Journal Article Butterfly pea (Clitoria ternatea), a cyclotide-bearing plant with applications in agriculture and medicineOguis, Georgianna K., Gilding, Edward K., Jackson, Mark A. and Craik, David J. (2019). Butterfly pea (Clitoria ternatea), a cyclotide-bearing plant with applications in agriculture and medicine. Frontiers in Plant Science, 10 645, 645. doi: 10.3389/fpls.2019.00645 |
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2019 Journal Article Rapid and scalable plant-based production of a potent plasmin inhibitor peptideJackson, Mark A., Yap, Kuok, Poth, Aaron G., Gilding, Edward K., Swedberg, Joakim E., Poon, Simon, Qu, Haiou, Durek, Thomas, Harris, Karen, Anderson, Marilyn A. and Craik, David J. (2019). Rapid and scalable plant-based production of a potent plasmin inhibitor peptide. Frontiers in Plant Science, 10 602, 602. doi: 10.3389/fpls.2019.00602 |
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2019 Journal Article NaV1.6 regulates excitability of mechanosensitive sensory neuronsIsrael, Mathilde R., Tanaka, Brian S., Castro, Joel, Thongyoo, Panumart, Robinson, Samuel D., Zhao, Peng, Deuis, Jennifer R., Craik, David J., Durek, Thomas, Brierley, Stuart M., Waxman, Stephen G, Dib-Hajj, Sulayman D. and Vetter, Irina (2019). NaV1.6 regulates excitability of mechanosensitive sensory neurons. Journal of Physiology, 597 (14), 3751-3768. doi: 10.1113/JP278148 |
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2019 Journal Article Molecular dynamics simulations of dihydro‐β‐erythroidine bound to the human α4β2 nicotinic acetylcholine receptorYu, Rilei, Tae, Han‐Shen, Xu, Qingliang, Craik, David J., Adams, David J., Jiang, Tao and Kaas, Quentin (2019). Molecular dynamics simulations of dihydro‐β‐erythroidine bound to the human α4β2 nicotinic acetylcholine receptor. British Journal of Pharmacology, 176 (15) bph.14698, 2750-2763. doi: 10.1111/bph.14698 |
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2019 Journal Article Salt-tolerant antifungal and antibacterial activities of the corn defensin ZmD32Kerenga, Bomai K., McKenna, James A., Harvey, Peta J., Quimbar, Pedro, Garcia-Ceron, Donovan, Lay, Fung T., Thanh Kha Phan,, Veneer, Prem K., Vasa, Shaily, Parisi, Kathy, Shafee, Thomas M. A., van der Weerden, Nicole L., Hulett, Mark D., Craik, David J., Anderson, Marilyn A. and Bleackley, Mark R. (2019). Salt-tolerant antifungal and antibacterial activities of the corn defensin ZmD32. Frontiers in Microbiology, 10 795, 795. doi: 10.3389/fmicb.2019.00795 |
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2019 Journal Article Papain-like cysteine proteases prepare plant cyclic peptide precursors for cyclizationRehm, Fabian B. H., Jackson, Mark A., De Geyter, Ewout, Yap, Kuok, Gilding, Edward K., Durek, Thomas and Craik, David J. (2019). Papain-like cysteine proteases prepare plant cyclic peptide precursors for cyclization. Proceedings of the National Academy of Sciences, 116 (16), 7831-7836. doi: 10.1073/pnas.1901807116 |
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2019 Journal Article Amino acid scanning at P5′ within the Bowman–Birk inhibitory loop reveals specificity trends for diverse serine proteasesLi, Choi Yi, de Veer, Simon J., White, Andrew M., Chen, Xingchen, Harris, Jonathan M., Swedberg, Joakim E. and Craik, David J. (2019). Amino acid scanning at P5′ within the Bowman–Birk inhibitory loop reveals specificity trends for diverse serine proteases. Journal of Medicinal Chemistry, 62 (7), 3696-3706. doi: 10.1021/acs.jmedchem.9b00211 |
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2019 Journal Article Toward structure determination of disulfide-rich peptides using chemical shift-based methodsWang, Conan K. and Craik, David J. (2019). Toward structure determination of disulfide-rich peptides using chemical shift-based methods. The Journal of Physical Chemistry B, 123 (9) acs.jpcb.8b10649, 1903-1912. doi: 10.1021/acs.jpcb.8b10649 |
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2019 Journal Article Where cone snails and spiders meet: design of small cyclic sodium-channel inhibitorsPeigneur, Steve, Cheneval, Olivier, Maiti, Mohitosh, Leipold, Enrico, Heinemann, Stefan H., Lescrinier, Eveline, Herdewijn, Piet, De Lima, Maria Elena, Craik, David J., Schroeder, Christina I. and Tytgat, Jan (2019). Where cone snails and spiders meet: design of small cyclic sodium-channel inhibitors. FASEB Journal, 33 (3), 3693-3703. doi: 10.1096/fj.201801909R |
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2019 Journal Article A centipede toxin family defines an ancient class of CSαβ defensinsDash, Thomas S., Shafee, Thomas, Harvey, Peta J., Zhang, Chuchu, Peigneur, Steve, Deuis, Jennifer R., Vetter, Irina, Tytgat, Jan, Anderson, Marilyn A., Craik, David J., Durek, Thomas and Undheim, Eivind A. B. (2019). A centipede toxin family defines an ancient class of CSαβ defensins. Structure, 27 (2), 315-326. doi: 10.1016/j.str.2018.10.022 |
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2019 Journal Article Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasmaSwedberg, Joakim E., Wu, Guojie, Mahatmanto, Tunjung, Durek, Thomas, Caradoc-Davies, Tom T., Whisstock, James C., Law, Ruby H. P. and Craik, David J. (2019). Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasma. Journal of Medicinal Chemistry, 62 (2), 552-560. doi: 10.1021/acs.jmedchem.8b01139 |
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2019 Journal Article Discovery and characterization of cyclic and acyclic trypsin inhibitors from Momordica dioicaDu, Junqiao, Chan, Lai Yue, Poth, Aaron G. and Craik, David J. (2019). Discovery and characterization of cyclic and acyclic trypsin inhibitors from Momordica dioica. Journal of Natural Products, 82 (2) acs.jnatprod.8b00716, 293-300. doi: 10.1021/acs.jnatprod.8b00716 |
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2019 Journal Article Peptide-membrane interactions affect the inhibitory potency and selectivity of spider toxins ProTx-II and GpTx-1Lawrence, Nicole, Wu, Bin, Ligutti, Joseph, Cheneval, Olivier, Agwa, Akello Joanna, Benfield, Aurélie H., Biswas, Kaustav, Craik, David J., Miranda, Les P., Henriques, Sónia Troeira and Schroeder, Christina I. (2019). Peptide-membrane interactions affect the inhibitory potency and selectivity of spider toxins ProTx-II and GpTx-1. ACS Chemical Biology, 14 (1), 118-130. doi: 10.1021/acschembio.8b00989 |
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2019 Journal Article Characterising the subsite specificity of urokinase-type plasminogen activator and tissue-type plasminogen activator using a sequence-defined peptide aldehyde libraryLi, Choi Yi, de Veer, Simon J., Law, Ruby H. P., Whisstock, James C., Craik, David J. and Swedberg, Joakim E. (2019). Characterising the subsite specificity of urokinase-type plasminogen activator and tissue-type plasminogen activator using a sequence-defined peptide aldehyde library. ChemBioChem, 19 (1), 46-50. doi: 10.1002/cbic.201800395 |
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2019 Journal Article Evaluation of the in vitro antitumor activity of nanostructured cyclotides in polymers of Eudragit (R) L 100-55 and RS 30 DSilva, Osmar N., Pinto, Michelle F. S., Viana, Juliane F. C., Freitas, Camila G., Fensterseifer, Isabel C. M., Craik, David J. and Franco, Octavio L. (2019). Evaluation of the in vitro antitumor activity of nanostructured cyclotides in polymers of Eudragit (R) L 100-55 and RS 30 D. Letters in Drug Design and Discovery, 16 (4), 437-445. doi: 10.2174/1570180815666180801115526 |
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2019 Book Chapter Cyclizing disulfide-rich peptides using sortase AAgwa, Akello J., Craik, David J. and Schroeder, Christina I. (2019). Cyclizing disulfide-rich peptides using sortase A. Methods in Molecular Biology. (pp. 29-41) edited by Timo Nuijens and Marcel Schmidt. New York, NY, United States: Humana Press. doi: 10.1007/978-1-4939-9546-2_3 |
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2019 Book Chapter Overview of NMR in the Pharmaceutical SciencesSchirra, Horst Joachim and Craik, David J. (2019). Overview of NMR in the Pharmaceutical Sciences. Modern Magnetic Resonance. (pp. 1195-1202) Dordrecht, Netherlands: Springer Netherlands. doi: 10.1007/1-4020-3910-7_128 |
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2018 Journal Article Mechanism of bacterial membrane permeabilization of crotalicidin (Ctn) and its fragment Ctn[15-34], antimicrobial peptides from rattlesnake venomPérez-Peinado, Clara, Almeida Dias, Susana, Domingues, Marco M., Benfield, Aurélie H., Freire, João Miguel, Radis-Baptista, Gandhi, Gaspar, Diana, Castanho, Miguel A. R. B., Craik, David J., Henriques, Sonia Troeira, Veiga, Ana S. and Andreu, David (2018). Mechanism of bacterial membrane permeabilization of crotalicidin (Ctn) and its fragment Ctn[15-34], antimicrobial peptides from rattlesnake venom. The Journal of Biological Chemistry, 293 (5), 1536-1549. doi: 10.1074/jbc.RA117.000125 |
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2018 Journal Article Potent, selective, and cell-penetrating inhibitors of Kallikrein-related peptidase 4 based on the cyclic peptide MCoTI-IISwedberg, Joakim E., Ghani, Hafiza Abdul, Harris, Jonathan M., de Veer, Simon J. and Craik, David J. (2018). Potent, selective, and cell-penetrating inhibitors of Kallikrein-related peptidase 4 based on the cyclic peptide MCoTI-II. ACS Medicinal Chemistry Letters, 9 (12) acsmedchemlett.8b00422, 1258-1262. doi: 10.1021/acsmedchemlett.8b00422 |
