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2017

Journal Article

Spider peptide toxin HwTx-IV engineered to bind to lipid membranes has an increased inhibitory potency at human voltage-gated sodium channel hNaV1.7

Agwa, Akello J., Lawrence, Nicole, Deplazes, Evelyne, Cheneval, Olivier, Chen, Rachel M., Craik, David J., Schroeder, Christina I. and Henriques, Sónia T. (2017). Spider peptide toxin HwTx-IV engineered to bind to lipid membranes has an increased inhibitory potency at human voltage-gated sodium channel hNaV1.7. Biochimica et Biophysica Acta. Biomembranes, 1859 (5), 835-844. doi: 10.1016/j.bbamem.2017.01.020

Spider peptide toxin HwTx-IV engineered to bind to lipid membranes has an increased inhibitory potency at human voltage-gated sodium channel hNaV1.7

2017

Journal Article

αO-Conotoxin GeXIVA disulfide bond isomers exhibit differential sensitivity for various nicotinic acetylcholine receptors but retain potency and selectivity for the human α9α10 subtype

Zhangsun, Dongting, Zhu, Xiaopeng, Kaas, Quentin, Wu, Yong, Craik, David J. , McIntosh, J. Michael and Luo, Sulan (2017). αO-Conotoxin GeXIVA disulfide bond isomers exhibit differential sensitivity for various nicotinic acetylcholine receptors but retain potency and selectivity for the human α9α10 subtype. Neuropharmacology, 127, 243-252. doi: 10.1016/j.neuropharm.2017.04.015

αO-Conotoxin GeXIVA disulfide bond isomers exhibit differential sensitivity for various nicotinic acetylcholine receptors but retain potency and selectivity for the human α9α10 subtype

2017

Journal Article

Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRET

Kubota, Tomoya, Durek, Thomas, Dang, Bobo, Finol-Urdaneta, Rocio K., Craik, David J., Kent, Stephen B. H., French, Robert J., Bezanilla, Francisco and Correa, Ana M. (2017). Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRET. Proceedings of the National Academy of Sciences, 114 (10), E1857-E1865. doi: 10.1073/pnas.1700453114

Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRET

2017

Journal Article

Orientation and location of the cyclotide kalata B1 in lipid bilayers revealed by solid-state NMR

Grage, Stephan L., Sani, Marc-Antoine, Cheneval, Olivier, Henriques, Sonia Troeira, Schalck, Constantin, Heinzmann, Ralf, Mylne, Joshua S., Mykhailiuk, Pavel K., Afonin, Sergii, Komarov, Igor V., Separovic, Frances, Craik, David J. and Ulrich, Anne S. (2017). Orientation and location of the cyclotide kalata B1 in lipid bilayers revealed by solid-state NMR. Biophysical Journal, 112 (4), 630-642. doi: 10.1016/j.bpj.2016.12.040

Orientation and location of the cyclotide kalata B1 in lipid bilayers revealed by solid-state NMR

2017

Journal Article

Cyclotide structure and function: the role of membrane binding and permeation

Troeira Henriques, Sonia and Craik, David J. (2017). Cyclotide structure and function: the role of membrane binding and permeation. Biochemistry, 56 (5), 669-682. doi: 10.1021/acs.biochem.6b01212

Cyclotide structure and function: the role of membrane binding and permeation

2017

Journal Article

Synthesis and protein engineering applications of cyclotides

Qu, Haiou, Smithies, Bronwyn J. , Durek, Thomas and Craik, David J. (2017). Synthesis and protein engineering applications of cyclotides. Australian Journal of Chemistry, 70 (2), 152-161. doi: 10.1071/CH16589

Synthesis and protein engineering applications of cyclotides

2017

Journal Article

Design of potent and selective cathepsin G inhibitors based on the sunflower trypsin inhibitor-1 scaffold

Swedberg, Joakim E., Li, Choi Yi, De Veer, Simon J., Wang, Conan K. and Craik, David J. (2017). Design of potent and selective cathepsin G inhibitors based on the sunflower trypsin inhibitor-1 scaffold. Journal of Medicinal Chemistry, 60 (2), 658-667. doi: 10.1021/acs.jmedchem.6b01509

Design of potent and selective cathepsin G inhibitors based on the sunflower trypsin inhibitor-1 scaffold

2017

Book Chapter

A practical guide to structural aspects of macrocycles (NMR, x-ray, and modeling)

Craik, David J., Kaas, Quentin and Wang, Conan K. (2017). A practical guide to structural aspects of macrocycles (NMR, x-ray, and modeling). Practical medicinal chemistry with macrocycles: Design, synthesis, and case studies. (pp. 25-57) edited by Eric Marsault and Mark L Peterson. Hoboken, New Jersey, United States: John Wiley & Sons. doi: 10.1002/9781119092599.ch2

A practical guide to structural aspects of macrocycles (NMR, x-ray, and modeling)

2017

Journal Article

Identification of survival-promoting OSIP108 peptide variants and their internalization in human cells

Verbandt, Sara, Henriques, Sónia Troeira, Spincemaille, Pieter, Harvey, Peta J., Chandhok, Gursimran, Sauer, Vanessa, De Coninck, Barbara, Cassiman, David, Craik, David J., Cammue, Bruno P. A., De Cremer, Kaat and Thevissen, Karin (2017). Identification of survival-promoting OSIP108 peptide variants and their internalization in human cells. Mechanisms of Ageing and Development, 161 (B), 247-254. doi: 10.1016/j.mad.2016.07.013

Identification of survival-promoting OSIP108 peptide variants and their internalization in human cells

2017

Conference Publication

Small molecule and peptidic ligands as PCSK9-LDLR inhibitors

Bhattacharya, Samit, Ammirati, Mark, Borzilleri, Kris, Cheneval, Olivier, Chrunyk, Boris, Craik, David, Daly, Norelle, Dullea, Robert, Griffor, Matthew, Kamlet, Adam, Limberakis, Chris, Sahasrabudhe, Parag, Liu, Shenping, Loria, Paula, Mc Clure, Kim, Menhaji-Klotz, Elnaz, Petersen, Donna, Piotrowski, David, Popovska-Gorevski, Marina, Price, David, Reyes, Allan, Ruggeri, Roger, Schroeder, Christina, Song, Kun, Swedberg, Joakim, Stock, Ingrid, Tu, Meihua and Withka, Jane (2017). Small molecule and peptidic ligands as PCSK9-LDLR inhibitors. 254th National Meeting and Exposition of the American-Chemical-Society (ACS) on Chemistry's Impact on the Global Economy, Washington, DC, 20-24 August 2017 . Washington, DC, United States: American Chemical Society.

Small molecule and peptidic ligands as PCSK9-LDLR inhibitors

2017

Book Chapter

Cyclotides: plant defense toxins

Oguis, Georgianna Kae, Kan, Meng-Wei and Craik, David J. (2017). Cyclotides: plant defense toxins. Plant toxins. (pp. 221-243) edited by P Gopalakrishnakone, Célia R Carlini and Rodrigo Ligabue-Braun. Dordrecht, The Netherlands: Springer, Dordrecht. doi: 10.1007/978-94-007-6464-4

Cyclotides: plant defense toxins

2017

Book Chapter

Cyclotides: plant defense toxins

Oguis, Georgianna Kae, Kan, Meng-Wei and Craik, David J. (2017). Cyclotides: plant defense toxins. Plant toxins. (pp. 221-242) edited by P. Gopalakrishnakone, Célia Regina Carlini and Rodrigo Ligabue-Braun. Dordrecht, Netherlands: Springer. doi: 10.1007/978-94-007-6464-4_7

Cyclotides: plant defense toxins

2017

Book Chapter

Naturally occurring disulfide-rich cyclic peptides from plants and animals: synthesis and biosynthesis

de Veer, Simon J. and Craik, David J. (2017). Naturally occurring disulfide-rich cyclic peptides from plants and animals: synthesis and biosynthesis. Chemical biology of natural products. (pp. 491-528) edited by David J. Newman, Gordon M. Cragg and Paul G. Grothaus. Boca Raton, FL, United States: CRC Press. doi: 10.1201/9781315117089-13

Naturally occurring disulfide-rich cyclic peptides from plants and animals: synthesis and biosynthesis

2017

Journal Article

Structural and functional characterization of chimeric cyclotides from the Möbius and trypsin inhibitor subfamilies

Abdul Ghani, Hafiza, Henriques, Sonia Troeira, Huang, Yen-Hua, Swedberg, Joakim E. , Schroeder, Christina I. and Craik, David J. (2017). Structural and functional characterization of chimeric cyclotides from the Möbius and trypsin inhibitor subfamilies. Biopolymers, 108 (1) e22927, e22927. doi: 10.1002/bip.22927

Structural and functional characterization of chimeric cyclotides from the Möbius and trypsin inhibitor subfamilies

2017

Book Chapter

Overview of NMR in drug design

Craik, David J. and Peacock, Hayden (2017). Overview of NMR in drug design. Modern magnetic resonance. (pp. 1-11) edited by Graham A. Webb. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-28275-6_112-1

Overview of NMR in drug design

2016

Journal Article

Isolation and characterization of cyclotides from Brazilian Psychotria: significance in plant defense and co-occurrence with antioxidant alkaloids

Matsuura, Helio N., Poth, Aaron G., Yendo, Anna C. A., Fett-Neto, Arthur G. and Craik, David J. (2016). Isolation and characterization of cyclotides from Brazilian Psychotria: significance in plant defense and co-occurrence with antioxidant alkaloids. Journal of Natural Products, 79 (12), 3006-3013. doi: 10.1021/acs.jnatprod.6b00492

Isolation and characterization of cyclotides from Brazilian Psychotria: significance in plant defense and co-occurrence with antioxidant alkaloids

2016

Journal Article

Discovery and optimization of peptide macrocycles

White, Andrew M. and Craik, David J. (2016). Discovery and optimization of peptide macrocycles. Expert Opinion on Drug Discovery, 11 (12), 1151-1163. doi: 10.1080/17460441.2016.1245720

Discovery and optimization of peptide macrocycles

2016

Journal Article

Characterization of a bioactive acyclotide from Palicourea rigida

Pinto, Michelle F. S., Silva, Osmar N., Viana, Juilan C., Porto, William F., Migliolo, Ludovico, da Cunha, Nicolau B., Gomes Jr., Nelson, Fensterseifer, Isabel C. M., Colgrave, Michelle L., Craik, David J., Dias, Simoni C. and Franco, Octavio L. (2016). Characterization of a bioactive acyclotide from Palicourea rigida. Journal of Natural Products, 79 (11), 2767-2773. doi: 10.1021/acs.jnatprod.6b00270

Characterization of a bioactive acyclotide from Palicourea rigida

2016

Journal Article

Cyclic peptide oral bioavailability: lessons from the past

Wang, Conan K. and Craik, David J. (2016). Cyclic peptide oral bioavailability: lessons from the past. Biopolymers, 106 (6), 901-909. doi: 10.1002/bip.22878

Cyclic peptide oral bioavailability: lessons from the past

2016

Journal Article

Effects of linker sequence modifications on the structure, stability and biological activity of a cyclic α-conotoxin

Carstens, Bodil B., Swedberg, Joakim, Berecki, Geza, Adams, David J., Craik, David J. and Clark, Richard J. (2016). Effects of linker sequence modifications on the structure, stability and biological activity of a cyclic α-conotoxin. Biopolymers, 106 (6), 864-875. doi: 10.1002/bip.22848

Effects of linker sequence modifications on the structure, stability and biological activity of a cyclic α-conotoxin