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2017

Book Chapter

A Strategy for production of correctly folded disulfide-rich peptides in the periplasm of E. coli

Saez, Natalie J., Cristofori-Armstrong, Ben, Anangi, Raveendra and King, Glenn F. (2017). A Strategy for production of correctly folded disulfide-rich peptides in the periplasm of E. coli. In Heterologous Gene Expression in E. coli Methods and Protocols (pp. 155-180) New York, NY United States: Humana Press. doi:10.1007/978-1-4939-6887-9_10

A Strategy for production of correctly folded disulfide-rich peptides in the periplasm of E. coli

2017

Conference Publication

Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders

Cardoso, Fernanda C., Bellingham, Mark C., King, Glenn F. and Lewis, Richard J. (2017). Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders. Venom to Drugs Conference 2017, Noosa Heads, QLD Australia, 9-14 October 2017.

Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders

2016

Journal Article

Centipede venoms as a source of drug leads

Undheim, Eivind A. B., Jenner, Ronald A. and King, Glenn F. (2016). Centipede venoms as a source of drug leads. Expert Opinion on Drug Discovery, 11 (12), 1139-1149. doi: 10.1080/17460441.2016.1235155

Centipede venoms as a source of drug leads

2016

Journal Article

Isolation of two insecticidal toxins from venom of the Australian theraphosid spider Coremiocnemis tropix

Ikonomopoulou, Maria P., Smith, Jennifer J., Herzig, Volker, Pineda, Sandy S., Dziemborowicz, Sławomir, Er, Sing-Yan, Durek, Thomas, Gilchrist, John, Alewood, Paul F., Nicholson, Graham M., Bosmans, Frank and King, Glenn F. (2016). Isolation of two insecticidal toxins from venom of the Australian theraphosid spider Coremiocnemis tropix. Toxicon, 123, 62-70. doi: 10.1016/j.toxicon.2016.10.013

Isolation of two insecticidal toxins from venom of the Australian theraphosid spider Coremiocnemis tropix

2016

Journal Article

Determination of ligand binding modes in weak protein–ligand complexes using sparse NMR data

Mohanty, Biswaranjan, Williams, Martin L., Doak, Bradley C., Vazirani, Mansha, Ilyichova, Olga, Wang, Geqing, Bermel, Wolfgang, Simpson, Jamie S., Chalmers, David K., King, Glenn F., Mobli, Mehdi and Scanlon, Martin J. (2016). Determination of ligand binding modes in weak protein–ligand complexes using sparse NMR data. Journal of Biomolecular NMR, 66 (3), 195-208. doi: 10.1007/s10858-016-0067-4

Determination of ligand binding modes in weak protein–ligand complexes using sparse NMR data

2016

Journal Article

Molecular basis of the interaction between gating modifier spider toxins and the voltage sensor of voltage-gated ion channels

Lau, Carus H.Y., King, Glenn F and Mobli, Mehdi (2016). Molecular basis of the interaction between gating modifier spider toxins and the voltage sensor of voltage-gated ion channels. Scientific Reports, 6 (1) 34333, 34333. doi: 10.1038/srep34333

Molecular basis of the interaction between gating modifier spider toxins and the voltage sensor of voltage-gated ion channels

2016

Journal Article

Interaction of tarantula venom peptide ProTx-II with lipid membranes is a prerequisite for its inhibition of human voltage-gated sodium channel NaV1.7

Troeira Henriques, Sonia, Deplazes, Evelyne, Lawrence, Nicole, Cheneval, Olivier, Chaousis, Stephanie, Inserra, Marco, Thongyoo, Panumart, King, Glenn F., Mark, Alan E., Vetter, Irina, Craik, David J. and Schroeder, Christina Ingrid (2016). Interaction of tarantula venom peptide ProTx-II with lipid membranes is a prerequisite for its inhibition of human voltage-gated sodium channel NaV1.7. The Journal of Biological Chemistry, 291 (33), 17049-17065. doi: 10.1074/jbc.M116.729095

Interaction of tarantula venom peptide ProTx-II with lipid membranes is a prerequisite for its inhibition of human voltage-gated sodium channel NaV1.7

2016

Journal Article

Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus

Touchard, Axel, Brust, Andreas, Cardoso, Fernanda C., Chin, K.-Y., Herzig, Volker, Jin, Ai-Hua, Dejean, Alain, Alewood, Paul F., King, Glenn F., Orivel, Jérôme and Escoubas, Pierre (2016). Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus. Biochimica et Biophysica Acta, 1860 (11 Part A), 2553-2562. doi: 10.1016/j.bbagen.2016.07.027

Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus

2016

Journal Article

Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury

Koehn, Liam M, Noor, Natassya M, Dong, Qing, Er, Sing-Yan, Rash, Lachlan D, King, Glenn F, Dziegielewska, Katarzyna M, Saunders, Norman R and Habgood, Mark D (2016). Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury. F1000Research, 5 1822, 1822. doi: 10.12688/f1000research.9094.2

Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury

2016

Journal Article

Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury [version 1; referees: 1 approved, 1 approved with reservations]

Koehn, Liam M., Dong, Qing, Er, Sing-Yan, Rash, Lachlan D., King, Glenn F., Dziegielewska, Katarzyna M., Saunders, Norman R. and Habgood, Mark D. (2016). Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury [version 1; referees: 1 approved, 1 approved with reservations]. F1000Research, 5 1822, 1822. doi: 10.12688/F1000RESEARCH.9094.1

Selective inhibition of ASIC1a confers functional and morphological neuroprotection following traumatic spinal cord injury [version 1; referees: 1 approved, 1 approved with reservations]

2016

Journal Article

Molecular basis of the remarkable species selectivity of an insecticidal sodium channel toxin from the African spider Augacephalus ezendami

Herzig, Volker, Ikonomopoulou, Maria, Smith, Jennifer J., Dziemborowicz, Slawomir, Gilchrist, John, Kuhn-Nentwig, Lucia, Rezende, Fernanda Oliveira, Moreira, Luciano Andrade, Nicholson, Graham M., Bosmans, Frank and King, Glenn F. (2016). Molecular basis of the remarkable species selectivity of an insecticidal sodium channel toxin from the African spider Augacephalus ezendami. Scientific Reports, 6 (1) 29538, 29538. doi: 10.1038/srep29538

Molecular basis of the remarkable species selectivity of an insecticidal sodium channel toxin from the African spider Augacephalus ezendami

2016

Journal Article

Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain

Osteen, Jeremiah D., Herzig, Volker, Gilchrist, John, Emrick, Joshua J., Zhang, Chuchu, Wang, Xidao, Castro, Joel, Garcia-Caraballo, Sonia, Grundy, Luke, Rychkov, Grigori Y., Weyer, Andy D., Dekan, Zoltan, Undheim, Eivind A. B., Alewood, Paul, Stucky, Cheryl L., Brierley, Stuart M., Basbaum, Allan I., Bosmans, Frank, King, Glenn F. and Julius, David (2016). Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain. Nature, 543 (7608), 494-499. doi: 10.1038/nature17976

Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain

2016

Journal Article

Toxin structures as evolutionary tools: Using conserved 3D folds to study the evolution of rapidly evolving peptides

Undheim, Eivind A., Mobli, Mehdi and King, Glenn F. (2016). Toxin structures as evolutionary tools: Using conserved 3D folds to study the evolution of rapidly evolving peptides. Bioessays, 38 (6), 539-548. doi: 10.1002/bies.201500165

Toxin structures as evolutionary tools: Using conserved 3D folds to study the evolution of rapidly evolving peptides

2016

Journal Article

Characterization of Three Venom Peptides from the Spitting Spider Scytodes thoracica

Ariki, Nathanial K., Muñoz, Lisa E., Armitage, Elizabeth L., Goodstein, Francesca R., George, Kathryn G, Smith, Vanessa L., Vetter, Irina, Herzig, Volker, King, Glenn F. and Loening, Nikolaus M. (2016). Characterization of Three Venom Peptides from the Spitting Spider Scytodes thoracica. PLoS One, 11 (5) e0156291, e0156291. doi: 10.1371/journal.pone.0156291

Characterization of Three Venom Peptides from the Spitting Spider Scytodes thoracica

2016

Conference Publication

Combining Mass Spectrometry Cross-Linking, Molecular Docking and NMR Titration to Dissect ZapA-FtsZ Protein Interaction

Caldas Nogueira, Maria Luiza, Sforca, Mauricio Luis, Paes Leme, Adriana Franco, Pauletti, Bianca Alves, Lopes de Oliveira, Paulo Sergio, Honorato, Rodrigo Vargas, King, Glenn F., Gueiros Filho, Frederico Jose and de Mattos Zeri, Ana Carolina (2016). Combining Mass Spectrometry Cross-Linking, Molecular Docking and NMR Titration to Dissect ZapA-FtsZ Protein Interaction. Experimental Biology Meeting, San Diego Ca, Apr 02-06, 2016. BETHESDA: FEDERATION AMER SOC EXP BIOL.

Combining Mass Spectrometry Cross-Linking, Molecular Docking and NMR Titration to Dissect ZapA-FtsZ Protein Interaction

2016

Conference Publication

Combining Mass Spectrometry Cross‐Linking, Molecular Docking and NMR Titration to Dissect ZapA‐FtsZ Protein Interaction

Nogueira, Maria Luiza Caldas, Sforça, Mauricio Luis, Leme, Adriana Franco Paes, Pauletti, Bianca Alves, de Oliveira, Paulo Sergio Lopes, Honorato, Rodrigo Vargas, King, Glenn F., Filho, Frederico José Gueiros and de Mattos Zeri, Ana Carolina (2016). Combining Mass Spectrometry Cross‐Linking, Molecular Docking and NMR Titration to Dissect ZapA‐FtsZ Protein Interaction. Experimental Biology 2016 Meeting, San Diego, CA United States, 1-5 April 2016. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1096/fasebj.30.1_supplement.lb60

Combining Mass Spectrometry Cross‐Linking, Molecular Docking and NMR Titration to Dissect ZapA‐FtsZ Protein Interaction

2016

Journal Article

Venoms of heteropteran insects: a treasure trove of diverse pharmacological toolkits

Walker, Andrew A., Weirauch, Christiane, Fry, Bryan G. and King, Glenn F. (2016). Venoms of heteropteran insects: a treasure trove of diverse pharmacological toolkits. Toxins, 8 (2) 43, 43. doi: 10.3390/toxins8020043

Venoms of heteropteran insects: a treasure trove of diverse pharmacological toolkits

2016

Journal Article

Membrane-binding properties of gating modifier and pore-blocking toxins: membrane interaction is not a prerequisite for modification of channel gating

Deplazes, Evelyne, Troeira Henriques, Sonia, Smith, Jennifer J., King, Glenn F., Craik, David J., Mark, Alan E. and Schroeder, Christina I. (2016). Membrane-binding properties of gating modifier and pore-blocking toxins: membrane interaction is not a prerequisite for modification of channel gating. Biochimica et Biophysica Acta - Biomembranes, 1858 (4), 872-882. doi: 10.1016/j.bbamem.2016.02.002

Membrane-binding properties of gating modifier and pore-blocking toxins: membrane interaction is not a prerequisite for modification of channel gating

2016

Conference Publication

Using Spider Venom Peptides as Molecular Tools for Understanding Voltage-Gated Sodium Channel Function

Herzig, V., Osteen, J. D., Bosmans, F., Julius, D. and King, G. F. (2016). Using Spider Venom Peptides as Molecular Tools for Understanding Voltage-Gated Sodium Channel Function. 34th European Peptide Symposium, Leipzig, Germany, 4‐9 September 2016. HOBOKEN: Wiley.

Using Spider Venom Peptides as Molecular Tools for Understanding Voltage-Gated Sodium Channel Function

2016

Conference Publication

Exploring the immunosuppressive potential of venom-derived molecules

Ryan, R., Ikonomopoulou, M., Haigh, O., Lutzky, V, Martinez, Jimenez R., Ratnatunga, C., Wong, Y., Rojas, Leal, I, Lopez, A., Fry, B., Herzig, V, King, G. and Miles, J. (2016). Exploring the immunosuppressive potential of venom-derived molecules. International Congress of Immunology (ICI), Melbourne, VIC, Australia, 21-26 August 2016. Weinheim, Germany: Wiley - VCH. doi: 10.1002/eji.201670200

Exploring the immunosuppressive potential of venom-derived molecules