Engelse naam: Laboratory for Toxicology and Pharmacology
Overkoepelend instituut: KU Leuven; Departement Farmaceutische en Farmacologische Wetenschappen (KULeuven)
Adres: O. & N.2
Herestraat 49B 922 3000 Leuven België
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Type: Wetenschappelijk
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1 Directeur: Hoofd van de onderzoeksgroep/afdeling 2 Mariene onderzoeker: Is werkzaam in deze groep en treedt op als (co)auteur in minstens één mariene publicatie in de laatste 5 jaar. 3 Gespecialiseerd personeel: Levert administratieve of technische ondersteuning aan het zeewetenschappelijk onderzoek.
Personen (16) |
Top | Publicaties | Project | Evenementen |
- Tytgat, Jan 1, 2
- An, Dongchen
- Bernaerts, Hans
- Bonneure, Arne 3
- Devi, Prabha
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- Gotink, Joachim 3
- Lebbe, Eline 2
- Loix, Sara 3
- Mille, Bea 2
- Moreels, Lien 2
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- Peigneur, Steve 2
- Pierre, Nele
- Pinheiro-Junior, Ernesto
- Seldeslachts, Andrea
- van Rooij, Milou 3
- Vijverman, Jenny
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Voormalig geassocieerde personen (12) |
- Abdel-Mottaleb, Yousra
- Billen, Bert
- Cassoli, Juliana
- Cologna, Camila
- Cuypers, Eva
- Debaveye, Sarah
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- Diego-García, Elia 2
- Galan, Diogo
- Goovaerts, Hannah
- Stevens, Marijke
- Van Der Haegen, Annelies
- Wijesekara, Isuru 2
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Abstract: |
Het laboratorium voor Toxicologie en Farmacologie van de KU Leuven doet onderzoek naar de werking van lichaamsvreemde stoffen (toxines) en naar de veiligheidsaspecten en samenstelling van voedselproducten. Hiernaast voert het laboratorium op vraag van diverse parketten/rechtbanken in België forensische toxicologische analyses en onderzoek uit op biologische stalen (inclusief post-mortem) en in beslag genomen producten.
Met betrekking tot het mariene thema, focust het labo op de ontdekking en karakterisering van toxines (peptiden en kleine organische moleculen) die aanwezig zijn in de gifklieren of organen van mariene soorten zoals kwallen, zeeanemonen en Conus slakken. De onderzoeksgroep wenst zich hier in de toekomst verder voor in te zetten. Een uitdaging binnen deze context vormt het combineren van state-of-the-art analytische technieken (chromatografie, massaspectrometrie, sequentiëren) teneinde proteomica te linken met transcriptonomica en functionele studies (door elektrofysiologische analyses gebruik makend van een voltage-klem op gekloonde ionenkanalen en receptoren).
Het laboratorium voor Toxicologie en Farmacologie participeerde tevens binnen het MAREX-project (2010-2014 - EU KP7) dat als doel had mariene hulpbronnen te onderzoeken op bioactieve stoffen. |
Publicaties (93) |
Top | Personen | Project | Evenementen |
( 84 peer reviewed ) opsplitsen filter
An, D.; Pinheiro-Junior, E.L.; Béress, L.; Gladkikh, I.; Leychenko, E.; Undheim, E.A.B.; Peigneur, S.; Tytgat, J. (2022). AsKC11, a Kunitz peptide from Anemonia sulcata, is a novel activator of G protein-coupled inward-rectifier potassium channels. Mar. Drugs 20(2): 140. https://dx.doi.org/10.3390/md20020140, meer
Kalina, R.S.; Kasheverov, I.E.; Koshelev, S.G.; Sintsova, O.V.; Peigneur, S.; Pinheiro-Junior, E.L.; Popov, R.S.; Chausova, V.; Monastyrnaya, M.M.; Dmitrenok, P.S.; Isaeva, M.P.; Tytgat, J.; Kozlov, S.A.; Kozlovskaya, E.P.; Leychenko, E.V.; Gladkikh, I.N. (2022). Nicotinic acetylcholine receptors are novel targets of APETx-like toxins from the sea anemone Heteractis magnifica. Toxins 14(10): 697. https://dx.doi.org/10.3390/toxins14100697, meer
Kvetkina, A.; Pislyagin, E.; Menchinskaya, E.; Yurchenko, E.; Kalina, R.; Kozlovskiy, S.; Kaluzhskiy, L.; Kim, N.; Peigneur, S.; Tytgat, J.; Ivanov, A.; Ayvazyan, N.; Leychenko, E.; Aminin, D. (2022). Kunitz-type peptides from sea anemones protect neuronal cells against Parkinson's disease inductors via inhibition of ROS production and ATP-induced P2X7 receptor activation. International Journal of Molecular Sciences 23(9): 5115. https://dx.doi.org/10.3390/ijms23095115, meer
Pinheiro-Junior, E.L.; Kalina, R.; Gladkikh, I.; Leychenko, E.; Tytgat, J.; Peigneur, S. (2022). A tale of toxin promiscuity: the versatile pharmacological effects of Hcr 1b-2 sea anemone peptide on voltage-gated ion channels. Mar. Drugs 20(2): 147. https://dx.doi.org/10.3390/md20020147, meer
Schmidt, C.A.; Cooke, I.; Wilson, D.T.; Miller, D.J.; Peigneur, S.; Tytgat, J.; Field, M.; Takjoo, R.; Smout, M.J.; Loukas, A.; Daly, N.L. (2022). Newly discovered peptides from the coral Heliofungia actiniformis show structural and functional diversity. J. Nat. Prod. 85(7): 1789-1798. https://dx.doi.org/10.1021/acs.jnatprod.2c00325, meer
Wiere, S.; Sugai, C.; Espiritu, M.J.; Aurelio, V.P.; Reyes, C.D.; Yuzon, N.; Whittal, R.M.; Tytgat, J.; Peigneur, S.; Bingham, J.-P. (2022). Research into the bioengineering of a novel α-conotoxin from the milked venom of Conus obscurus. International Journal of Molecular Sciences 23(20): 12096. https://dx.doi.org/10.3390/ijms232012096, meer
Jacobsson, E.; Peigneur, S.; Andersson, H.S.; Laborde, Q.; Strand, M.; Tytgat, J.; Goransson, U. (2021). Functional characterization of the nemertide α family of peptide toxins. J. Nat. Prod. 84(8): 2121-2128. https://dx.doi.org/10.1021/acs.jnatprod.1c00104, meer
Sintsova, O.; Gladkikh, I.; Monastyrnaya, M.; Tabakmakher, V.; Yurchenko, E.; Menchinskaya, E.; Pislyagin, E.; Andreev, Y.; Kozlov, S.; Peigneur, S.; Tytgat, J.; Aminin, D.; Kozlovskaya, E.; Leychenko, E. (2021). Sea anemone Kunitz-type peptides demonstrate neuroprotective activity in the 6-hydroxydopamine induced neurotoxicity model. Biomedicines 9(3): 283. https://hdl.handle.net/10.3390/biomedicines9030283, meer
Gladkikh, I.; Peigneur, S.; Sintsova, O.; Pinheiro-Junior, E.L.; Klimovich, A.; Menshov, A.; Kalinovsky, A.; Isaeva, M.; Monastyrnaya, M.; Kozlovskaya, E.; Tytgat, J.; Leychenko, E. (2020). Kunitz-type peptides from the sea anemone Heteractis crispa demonstrate potassium channel blocking and anti-inflammatory activities. Biomedicines 8(11): 473. https://hdl.handle.net/10.3390/biomedicines8110473, meer
Kalina, R.S.; Peigneur, S.; Zelepuga, E.A.; Dmitrenok, P.S.; Kvetkina, A.N.; Kim, N.Y.; Leychenko, E.V.; Tytgat, J.; Kozlovskaya, E.P.; Monastyrnaya, M.M.; Gladkikh, I.N. (2020). New insights into the type II toxins from the sea anemone Heteractis crispa. Toxins 12(1): 44. https://hdl.handle.net/10.3390/toxins12010044, meer
Kalina, R.S.; Peigneur, S.; Gladkikh, I.N.; Dmitrenok, P.S.; Kim, N.Y.; Leychenko, E.V.; Monastyrnaya, M.M.; Tytgat, J.; Kozlovskaya, E.P. (2020). New sea anemone toxin RTX-VI selectively modulates voltage-gated sodium channels. Doklady Biochemistry and Biophysics 495(1): 292-295. https://hdl.handle.net/10.1134/S1607672920060071, meer
Kvetkina, A.; Leychenko, E.; Chausova, V.; Zelepuga, E.; Chernysheva, N.; Guzev, K.; Pislyagin, E.; Yurchenko, E.; Menchinskaya, E.; Aminin, D.; Kaluzhskiy, L.; Ivanov, A.; Peigneur, S.; Tytgat, J.; Kozlovskaya, E.; Isaeva, M. (2020). A new multigene HCIQ subfamily from the sea anemone Heteractis crispa encodes Kunitz-peptides exhibiting neuroprotective activity against 6-hydroxydopamine. NPG Scientific Reports 10(1): 4205. https://hdl.handle.net/10.1038/s41598-020-61034-x, meer
Schmidt, C.A.; Wilson, D.T.; Cooke, I.; Potriquet, J.; Tungatt, K.; Muruganandah, V.; Boote, C.; Kuek, F.; Miles, J.J.; Kupz, A.; Ryan, S.; Loukas, A.; Bansal, P.S.; Takjoo, R.; Miller, D.J.; Peigneur, S.; Tytgat, J.; Daly, N.L. (2020). Identification and characterization of a peptide from the stony coral Heliofungia actiniformis. J. Nat. Prod. 83(11): 3454-3463. https://hdl.handle.net/10.1021/acs.jnatprod.0c00981, meer
Andersson, H.S.; Jacobsson, E.; Strand, M.; Peigneur, S.; Lebbe, E.K.M.; Rosengren, K.J.; Goransson, U.; Tytgat, J. (2019). α-nemertides, a novel family of marine peptide neurotoxins from ribbon worms. Toxicon 158(S1): S38-S39. https://hdl.handle.net/10.1016/j.toxicon.2018.10.136, meer
Collins, J.E.; Harden-Davies, H.; Jaspars, M.; Thiele, T.; Vanagt, T.; Huys, I. (2019). Inclusive innovation: Enhancing global participation in and benefit sharing linked to the utilization of marine genetic resources from areas beyond national jurisdiction. Mar. Policy 109: 103696. https://dx.doi.org/10.1016/j.marpol.2019.103696, meer
Elnahriry, K.A.; Wai, D.C.C.; Krishnarjuna, B.; Badawy, N.N.; Chittoor, B.; MacRaild, C.A.; Williams-Noonan, B.J.; Surm, J.M.; Chalmers, D.K.; Zhang, A.H.; Peigneur, S.; Mobli, M.; Tytgat, J.; Prentis, P.; Norton, R.S. (2019). Structural and functional characterisation of a novel peptide from the Australian sea anemone Actinia tenebrosa. Toxicon 168: 104-112. https://dx.doi.org/10.1016/j.toxicon.2019.07.002, meer
Gladkikh, I.; Kalina, R.; Sinsova, O.; Kvetkina, A.; Peigneur, S.; Koshelev, S.; Kim, N.; Monastyrnaya, M.; Kozlov, S.; Tytgat, J.; Kozlovskaya, E. (2019). New Kv, NAv, and ASIC channel toxins from the sea anemone Heteractis crispa. Toxicon 158(S1): S48-S48. https://hdl.handle.net/10.1016/j.toxicon.2018.10.168, meer
Kalina, R.; Gladkikh, I.; Peigneur, S.; Dmitrenok, P.; Zelepuga, E.; Monastyrnaya, M.; Kozlovskaya, E. (2019). Type II toxins from sea anemone Heteractis crispa with various effects on activation and inactivation of voltage-gated sodium channels. Toxicon 159(S1): S18-S18. https://hdl.handle.net/10.1016/j.toxicon.2018.11.376, meer
Peigneur, S.; Devi, P.; Seldeslachts, A.; Ravichandran, S.; Quinton, L.; Tytgat, J. (2019). Structure-function elucidation of a new α-conotoxin, MiIIA, from Conus milneedwardsi. Mar. Drugs 17(9): 535. https://dx.doi.org/10.3390/md17090535, meer
Peigneur, S.; Cheneval, O.; Maiti, M.; Leipold, E.; Heinemann, S.H.; Lescrinier, E.; Herdewijn, P.; de Lima, M.E.; Craik, D.J.; Schroeder, C.I.; Tytgat, J. (2019). Where cone snails and spiders meet: design of small cyclic sodium-channel inhibitors. FASEB J. 33(3): 3693-3703. https://dx.doi.org/10.1096/fj.201801909R, meer
Sachkova, M.Y.; Singer, S.A.; Macrander, J.; Reitzel, A.M.; Peigneur, S.; Tytgat, J.; Moran, Y. (2019). The birth and death of toxins with distinct functions: a case study in the sea anemone Nematostella. Mol. Biol. Evol. 36(9): 2001-2012. https://dx.doi.org/10.1093/molbev/msz132, meer
Sintsova, O.; Kalinovskii, A.; Gladkikh, I.; Zelepuga, E.; Monastyrnaya, M.; Kim, N.; Shevchenko, L.; Peigneur, S.; Tytgat, J.; Kozlovskaya, E.; Leychenko, E. (2019). Magnificamide, a β-defensin-like peptide from the mucus of the sea anemone Heteractis magnifica, is a strong inhibitor of mammalian α-amylases. Mar. Drugs 17(10): 542. https://dx.doi.org/10.3390/md17100542, meer
Zelepuga, E.; Gladkikh, I.; Peigneur, S.; Tytgat, J.; Monastyrnaya, M.; Kozlovskaya, E. (2019). The Kunitz-type HCRG peptides from the sea anemone Heteractis crispa possess Kv channel toxicity. Toxicon 159(S1): S26-S27. https://hdl.handle.net/10.1016/j.toxicon.2018.11.408, meer
Jacobsson, E.; Andersson, H.S.; Strand, M.; Peigneur, S.; Eriksson, C.; Loden, H.; Shariatgorji, M.; Andren, P.E.; Lebbe, E.K.M.; Rosengren, K.J.; Tytgat, J.; Goransson, U. (2018). Peptide ion channel toxins from the bootlace worm, the longest animal on Earth. NPG Scientific Reports 8: 10. https://dx.doi.org/10.1038/s41598-018-22305-w, meer
Krishnarjuna, B.; MacRaild, C.A.; Sunanda, P.; Morales, R.A.V.; Peigneur, S.; Macrander, J.; Yu, H.H.; Daly, M.; Raghothama, S.; Dhawan, V.; Chauhan, S.; Tytgat, J.; Pennington, M.W.; Norton, R.S. (2018). Structure, folding and stability of a minimal homologue from Anemonia sulcata of the sea anemone potassium channel blocker ShK. Peptides (New York, NY : 1980) 99: 169-178. https://dx.doi.org/10.1016/j.peptides.2017.10.001, meer
Krishnarjuna, B.; MacRaild, C.A.; Sunanda, P.; Morales, R.A.V.; Peigneur, S.; Macrander, J.; Yu, H.H.; Daly, M.; Raghothama, S.; Chauhan, S.; Tytgat, J.; Pennington, M.W.; Norton, R.S. (2018). Corrigendum to“Structure, folding and stability of a minimal homologue from Anemonia sulcata of the sea anemone potassium channel blocker ShK”[Peptides 99 (2018) 169–178]. Peptides (New York, NY : 1980) 101: 234-234. https://dx.doi.org/10.1016/j.peptides.2018.01.008, meer
Krishnarjuna, B.; Villegas-Moreno, J.; Mitchell, M.L.; Csoti, A.; Peigneur, S.; Amero, C.; Pennington, M.W.; Tytgat, J.; Panyi, G.; Norton, R.S. (2018). Synthesis, folding, structure and activity of a predicted peptide from the sea anemone Oulactis sp. with an ShKT fold. Toxicon 150: 50-59. https://dx.doi.org/10.1016/j.toxicon.2018.05.006, meer
Madio, B.; Peigneur, S.; Chin, Y.K.Y.; Hamilton, B.; Henriques, S.T.; Smith, J.J.; Cristofori-Armstrong, B.; Dekan, Z.; Boughton, B.A.; Alewood, P.F.; Tytgat, J.; King, G.F.; Undheim, E.A.B. (2018). PHAB toxins: a unique family of predatory sea anemone toxins evolving via intra-gene concerted evolution defines a new peptide fold. Cellular and molecular life sciences 75(24): 4511-4524. https://dx.doi.org/10.1007/s00018-018-2897-6, meer
Orts, D.J.B.; Peigneur, S.; Silva-Goncalves, L.C.; Arcisio-Miranda, M.; Bicudo, J.E.P.W.; Tytgat, J. (2018). AbeTx1 is a novel sea anemone toxin with a dual mechanism of action on Shaker-type K+ channels activation. Mar. Drugs 16(10): 360. https://dx.doi.org/10.3390/md16100360, meer
Peigneur, S.; de Lima, M.E.; Tytgat, J. (2018). Phoneutria nigriventer venom: a pharmacological treasure. Toxicon 151: 96-110. https://dx.doi.org/10.1016/j.toxicon.2018.07.008, meer
Rodríguez, A.A.; Garateix, A.; Salceda, E.; Peigneur, S.; Zaharenko, A.J.; Pons, T.; Santos, Y.; Arreguin, R.; Ständker, L.; Forssmann, W.-G.; Tytgat, J.; Vega, R.; Soto, E. (2018). PhcrTx2, a new crab-paralyzing peptide toxin from the sea anemone Phymanthus crucifer. Toxins 10(2): 72. https://dx.doi.org/10.3390/toxins10020072, meer
Sunanda, P.; Krishnarjuna, B.; Peigneur, S.; Mitchell, M.L.; Estrada, R.; Villegas-Moreno, J.; Pennington, M.W.; Tytgat, J.; Norton, R.S. (2018). Identification, chemical synthesis, structure, and function of a new KV1 channel blocking peptide from Oulactis sp. Peptide Science 110(4): e24073. https://dx.doi.org/10.1002/pep2.24073, meer
Montero-Alejo, V.; Corzo, G.; Porro-Suardiaz, J.; Pardo-Ruiz, Z.; Perera, E.; Rodriguez-Viera, L.; Sanchez-Diaz, G.; Alvarez, C.; Peigneur, S.; Tytgat, J.; Perdomo-Morales, R. (2017). Panusin represents a new family of β-defensin-like peptides in invertebrates. Dev. Comp. Immunol. 67: 310-321. https://dx.doi.org/10.1016/j.dci.2016.09.002, meer
Moreels, L.; Bhat, C.; Vorácová, M.; Peigneur, S.; Mäki-Lohiluoma, E.; Zahed, F.; Pardo, L.A.; Yli-Kauhaluoma, J.; Kiuru, P.; Tytgat, J. (2017). Synthesis of novel purpurealidin analogs and evaluation of their effect on the cancerrelevant potassium channel KV10.1. PLoS One 12(12): e0188811. https://dx.doi.org/10.1371/journal.pone.0188811, meer
Moreels, L.; Peigneur, S.; Galan, D.T.; De Pauw, E.; Béress, L.; Waelkens, E.; Pardo, L.A.; Quinton, L.; Tytgat, J. (2017). APETx4, a novel sea anemone toxin and a modulator of the cancer-relevant potassium channel KV10.1. Mar. Drugs 15(9): 287. https://dx.doi.org/10.3390/md15090287, meer
Zidar, N.; Zula, A.; Tomašic, T.; Rogers, M.; Kirby, R.W.; Tytgat, J.; Peigneur, S.; Kikelj, D.; Ilas, J.; Masic, L.P. (2017). Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels. Eur. J. Med. Chem. 139: 232-241. https://dx.doi.org/10.1016/j.ejmech.2017.08.015, meer
García-Fernández, R.; Peigneur, S.; Pons, T.; Alvarez, C.; González, L.; Chávez, M.A.; Tytgat, J. (2016). The Kunitz-type protein ShPI-1 inhibits serine proteases and voltage-gated potassium channels. Toxins 8(4): 110. dx.doi.org/10.3390/toxins8040110, meer
Kopljar, I.; Grottesi, A.; de Block, T.; Rainier, J.D.; Tytgat, J.; Labro, A.J.; Snyders, D.J. (2016). Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels. Neuropharmacology 107: 160-167. https://dx.doi.org/10.1016/j.neuropharm.2016.03.010, meer
Lebbe, E.K.M.; Ghequire, M.G.K.; Peigneur, S.; Mille, B.G.; Devi, P.; Ravichandran, S.; Waelkens, E.; D'Souza, L.; De Mot, R.; Tytgat, J. (2016). Novel conopeptides of largely unexplored Indo Pacific Conus sp. Mar. Drugs 14(11): 18 pp. https://dx.doi.org/10.3390/md14110199, meer
Lebbe, E.K.M.; Tytgat, J. (2016). In the picture: disulfide-poor conopeptides, a class of pharmacologically interesting compounds. Journal of Venomous Animals and Toxins Including Tropical Diseases 22: 15 pp. https://dx.doi.org/10.1186/s40409-016-0083-6, meer
Martínez-Morales, E.; Kopljar, I.; Rainier, J.D.; Tytgat, J.; Snyders, D.J.; Labro, A.J. (2016). Gambierol and n-alkanols inhibit Shaker Kv channel via distinct binding sites outside the K+ pore. Toxicon 120: 57-60. https://dx.doi.org/10.1016/j.toxicon.2016.07.017, meer
Monastyrnaya, M.; Peigneur, S.; Zelepuga, E.; Sintsova, O.; Gladkikh, I.; Leychenko, E.; Isaeva, M.; Tytgat, J.; Kozlovskaya, E. (2016). Kunitz-type peptide HCRG21 from the sea anemone Heteractis crispa is a full antagonist of the TRPV1 receptor. Mar. Drugs 14(12): 229. https://dx.doi.org/10.3390/md14120229, meer
Jukic, M.; Frlan, R.; Chan, F.; Kirby, R.; Madge, D.; Tytgat, J.; Peigneur, S.; Anderluh, M.; Kikelj, D. (2015). Synthesis and biological evaluation of piperazine derivatives as novel isoform selective voltage-gated sodium (Nav) 1.3 channel modulators. Med. Chem. Res. 24(6): 2366-2380. dx.doi.org/10.1007/s00044-014-1300-x, meer
Sintsova, O.; Chausova, V.; Gladkikh, I.; Isaeva, M.; Tabakmaher, V.; Monastyrnaya, M.; Leychenko, E.; Pislyagin, E.; Menchinskaya, E.; Peigneur, S.; Tytgat, J.; Kozlovskaya, E. (2015). New antihistamine Kunitz-type polypeptides of the sea anemones, Heteractis crispa and Stichodactyla mertensii. The FEBS Journal 282(Suppl. 1): 140-141, meer
Zelepuga, E.; Gladkikh, I.; Monastyrnaya, M.; Sintsova, O.; Tabakmaher, V.; Peigneur, S.; Tytgat, J.; Kozlovskaya, E. (2015). The sea anemone Heteractis crispa - a source of potential pharmacological agents. The FEBS Journal 282(Suppl. 1): 322-323, meer
Lebbe, E.K.M.; Peigneur, S.; Wijesekara, I.; Tytgat, J. (2014). Conotoxins targeting nicotinic acetylcholine receptors: an overview. Mar. Drugs 12(5): 2970-3004. dx.doi.org/10.3390/md12052970, meer
Lebbe, E.K.M.; Peigneur, S.; Maiti, M.; Devi, P; Ravichandran, S; D'Souza, L; Lescrinier, E.; Herdewijn, P.; Tytgat, J. (2014). Structure-function elucidation of a new alpha-conotoxin, Lo1a, from Conus longurionis. Toxicon 91: 170-171. dx.doi.org/10.1016/j.toxicon.2014.08.023, meer
Lebbe, E.K.M.; Peigneur, S.; Maiti, M.; Devi, P.; Ravichandran, S.; Lescrinier, E.; Ulens, C.; Waelkens, E.; D'Souza, L.; Herdewijn, P.; Tytgat, J. (2014). Structure-function elucidation of a new alpha-conotoxin, Lo1a, from Conus longurionis. J. Biol. Chem. 289(14): 9573-9583. https://dx.doi.org/10.1074/jbc.M114.556175, meer
Lebbe, E.K.M.; Peigneur, S.; Maiti, M.; Mille, B.G.; Devi, P; Ravichandran, S; Lescrinier, E.; Waelkens, E.; D'Souza, L; Herdewijn, P.; Tytgat, J. (2014). Discovery of a new subclass of alpha-conotoxins in the venom of Conus australis. Toxicon 91: 145-154. https://dx.doi.org/10.1016/j.toxicon.2014.08.074, meer
Peigneur, S.; Zula, A; Zidar, N; Chan-Porter, F; Kirby, R; Madge, D; Ilas, J; Kikelj, D; Tytgat, J. (2014). Action of Clathrodin and analogues on voltage-gated sodium channels. Mar. Drugs 12(4): 2132-2143. dx.doi.org/10.3390/md12042132, meer
Peigneur, S.; Tytgat, J. (2014). When cone snails and spiders meet: design of selective and potent sodium channel inhibitors. Toxicon 91: 170-170. dx.doi.org/10.1016/j.toxicon.2014.08.022, meer
Rodriguez, A; Salceda, E; Garateix, G; Zaharenko, J; Peigneur, S.; Lopez, O; Pons, T; Richardson, M; Diaz, M; Hernandez, Y; Standker, L; Tytgat, J.; Soto, E (2014). A novel sea anemone peptide that inhibits acid-sensing ion channels. Peptides (New York, NY : 1980) 53: 3-12. dx.doi.org/10.1016/j.peptides.2013.06.003, meer
Tytgat, J. (2014). Sea anemone toxins: from lab bench discovery to commercial drugs? Toxicon 91: 170-170. dx.doi.org/10.1016/j.toxicon.2014.08.021, meer
Wijesekara, I.; Peigneur, S.; Devi, P; Ravichandran, S; Lebbe, E.; Mille, B.; D'Souza, L; Tytgat, J. (2014). Isolation and characterization of novel conopeptides from Conus amadis that target voltage-gated sodium channels. Toxicon 91: 184-184. dx.doi.org/10.1016/j.toxicon.2014.08.056, meer
Zhu, S.; Peigneur, S.; Gao, B.; Umetsu, Y.; Ohki, S.; Tytgat, J. (2014). Experimental conversion of a defensin into a neurotoxin: Implications for origin of toxic function. Mol. Biol. Evol. 31(3): 546-559. https://dx.doi.org/10.1093/molbev/msu038, meer
Zidar, N.; Jakopin, Z.; Madge, D.; Chan, F.; Tytgat, J.; Peigneur, S.; Dolenc, M.; Tomasic, T.; Ilas, J.; Masic, L.; Kikelj, D. (2014). Substituted 4-phenyl-2-aminoimidazoles and 4-phenyl-4,5-dihydro-2-aminoimidazoles as voltage-gated sodium channel modulators. Eur. J. Med. Chem. 74: 23-30. dx.doi.org/10.1016/j.ejmech.2013.12.034, meer
Bergeron, Z.L.; Chun, J.B.; Baker, M.R.; Sandall, D.W.; Peigneur, S.; Yu, P.Y.C.; Thapa, P.; Milisen, J.W.; Tytgat, J.; Livett, B.G.; Bingham, J.P. (2013). A 'conovenomic' analysis of the milked venom from the mollusk-hunting cone snail Conus textile-The pharmacological importance of post-translational modifications. Peptides (New York, NY : 1980) 49: 145-158. dx.doi.org/10.1016/j.peptides.2013.09.004, meer
Cassoli, J.; Verano-Braga, T.; Oliveira, J.; Montandon, G.; Cologna, C.T.; Peigneur, S.; Pimenta, A.; Kjeldsen, F.; Roepstorff, P.; Tytgat, J.; de Lima, M. (2013). The proteomic profile of Stichodactyla duerdeni secretion reveals the presence of a novel O-linked glycopeptide. J. Proteomics 87: 89-102. https://dx.doi.org/10.1016/j.jprot.2013.05.022, meer
Kendel, Y.; Melaun, C.; Kurz, A.; Nicke, A.; Peigneur, S.; Tytgat, J.; Wunder, C.; Mebs, D.; Kauferstein, S. (2013). Venomous secretions from marine snails of the Terebridae family target acetylcholine receptors. Toxins 5(5): 1043-1050. dx.doi.org/10.3390/toxins5051043, meer
Kopljar, I.; Labro, A.J.; de Block, T.; Rainier, J.; Tytgat, J.; Snyders, D.J. (2013). The ladder-shaped polyether toxin gambierol anchors the gating machinery of Kv3.1 channels in the resting state. J. Gen. Physiol. 141(3): 359-369. https://dx.doi.org/10.1085/jgp.201210890, meer
Orts, D.J.B.; Peigneur, S.; Madio, B.; Cassoli, J.S.; Montandon, G.G.; Pimenta, A.M.C.; Bicudo, J.E.P.W.; Freitas, J.C.; Zaharenko, A.J.; Tytgat, J. (2013). Biochemical and electrophysiological characterization of two sea anemone Type 1 Potassium toxins from a geographically distant population of Bunodosoma caissarum. Mar. Drugs 11(3): 655-679. dx.doi.org/10.3390/md11030655, meer
Orts, D.J.B.; Moran, Y.; Cologna, C.T.; Peigneur, S.; Madio, B.; Praher, D.; Quinton, L.; De Pauw, E.; Bicudo, J.E.P.W.; Tytgat, J.; de Freitas, J.C. (2013). BcsTx3 is a founder of a novel sea anemone toxin family of potassium channel blocker. The FEBS Journal 280(19): 4839-4852. dx.doi.org/10.1111/febs.12456, meer
Peigneur, S.; Van Der Haegen, A.; Möller, C.; Waelkens, E.; Diego-García, E.; Marí, F.; Naudé, R.; Tytgat, J. (2013). Unraveling the peptidome of the South African cone snails Conus pictus and Conus natalis. Peptides (New York, NY : 1980) 41: 8-16. https://dx.doi.org/10.1016/j.peptides.2012.07.002, meer
Tomašic, T.; Hartzoulakis, B.; Zidar, N.; Chan, F.; Kirby, R.W.; Madge, D.J.; Peigneur, S.; Tytgat, J.; Kikelj, D. (2013). Ligand- and structure-based virtual screening for clathrodin-derived human voltage-gated sodium channel modulators. Journal of Chemical Information and Modeling 53(12): 3223-3232. https://dx.doi.org/10.1021/ci400505e, meer
Gladkikh, I.; Monastyrnaya, M.; Leychenko, E.; Zelepuga, E.; Chausova, V.; Isaeva, M.; Anastyuk, S.; Andreev, Y.; Peigneur, S.; Tytgat, J.; Kozlovkaya, E. (2012). Atypical reactive center Kunitz-type inhibitor from the sea anemone Heteractis crispa. Mar. Drugs 10(7): 1545-1565. http://dx.doi.org/10.3390/md10071545, meer
Kopljar, I.; Labro, A.J.; Rainier, J.D.; Tytgat, J.; Snyders, D.J. (2012). Voltage sensor trapping in voltage-gated K-channels by the marine neurotoxin Gambierol. Toxicon 60(2): 150-151. dx.doi.org/10.1016/j.toxicon.2012.04.111, meer
Peigneur, S.; Lescrinier, E.; Moller, C.; Mari, F.; Beress, L.; Tytgat, J. (2012). A natural point mutation reveals target promiscuity of toxins isolated from the sea anemone Anthopleura elegantissima. Biophys. J. 102(3, Supplement 1): 658A-658A, meer
Peigneur, S.; Béress, L.; Möller, C.; Marí, F.; Forssmann, W.-G.; Tytgat, J. (2012). A natural point mutation changes both target selectivity and mechanism of action of sea anemone toxins. FASEB J. 26(12): 5141-5151. http://dx.doi.org/10.1096/fj.12-218479, meer
Stevens, M.; Peigneur, S.; Dyubankova, N.; Lescrinier, E.; Herdewijn, P.; Tytgat, J. (2012). Design of bioactive peptides from naturally occurring µ-conotoxin structures. J. Biol. Chem. 287(37): 31382-31392. dx.doi.org/10.1074/jbc.M112.375733, meer
Van Der Haegen, A.; Peigneur, S.; Dyubankova, N.; Moller, C.; Mari, F.; Diego-García, E.; Naude, R.; Lescrinier, E.; Herdewijn, P.; Tytgat, J. (2012). Pc16a, the first characterized peptide from Conus pictus venom, shows a novel disulfide connectivity. Peptides (New York, NY : 1980) 34(1): 106-113. dx.doi.org/10.1016/j.peptides.2011.10.026, meer
Cuypers, E.; Peigneur, S.; Debaveye, S.; Shiomi, K.; Tytgat, J. (2011). TRPV1 channel as new target for marine toxins: Example of gigantoxin I, a sea anemone toxin acting via modulation of the PLA2 pathway. Acta Chim. Slov. 58(4): 735-741, meer
Peigneur, S.; Billen, B.; Derua, R.; Waelkens, E.; Debaveye, S.; Béress, L.; Tytgat, J. (2011). A bifunctional sea anemone peptide with Kunitz type protease and potassium channel inhibiting properties. Biochem. Pharmacol. 82(1): 81-90. https://dx.doi.org/10.1016/j.bcp.2011.03.023, meer
Van Der Haegen, A.; Peigneur, S.; Tytgat, J. (2011). Importance of position 8 in μ-conotoxin KIIIA for voltage-gated sodium channel selectivity. The FEBS Journal 278(18): 3408-3418. dx.doi.org/10.1111/j.1742-4658.2011.08264.x, meer
Billen, B.; Debaveye, S.; Béress, L.; Garateixand, A.; Tytgat, J. (2010). Phyla- and subtype-selectivity of CgNa, a Na+ channel toxin from the venom of the Giant Caribbean Sea Anemone Condylactis gigantea. Front. Pharmacol. 1: 133. http://dx.doi.org/10.3389/fphar.2010.00133, meer
Kopljar, I.; Labro, A.J.; Cuypers, E.; Johnson, H.W.B.; Rainier, J.D.; Tytgat, J.; Snyders, D.J. (2009). A polyether biotoxin binding site on the lipid-exposed face of the pore domain of Kv channels revealed by the marine toxin gambierol. Proc. Natl. Acad. Sci. U.S.A. 106(24): 9896-9901. http://dx.doi.org/10.1073/pnas.0812471106, meer
Cuypers, E.; Abdel-Mottaleb, Y.; Kopljar, I.; Rainier, J.; Raes, A.L.; Snyders, D.J.; Tytgat, J. (2008). Gambierol, a toxin produced by the dinoflagellate Gambierdiscus toxicus, is a potent blocker of voltage-gated potassium channels. Toxicon 51(6): 974-983. https://dx.doi.org/10.1016/j.toxicon.2008.01.004, meer
Bosmans, F.; Tytgat, J. (2007). Sea anemone venom as a source of insecticidal peptides acting on voltage-gated Na+ channels. Toxicon 49(4): 550-560. dx.doi.org/10.1016/j.toxicon.2006.11.029, meer
Cuypers, E.; Yanagihara, A.; Rainier, J.D.; Tytgat, J. (2007). TRPV1 as a key determinant in ciguatera and neurotoxic shellfish poisoning. Biochem. Biophys. Res. Commun. 361(1): 214-217. dx.doi.org/10.1016/j.bbrc.2007.07.009, meer
Cuypers, E.; Yanagihara, A.; Karlsson, E.; Tytgat, J. (2007). Corrigendum to "Jellyfish and other cnidarian envenomations cause pain by affecting TRPV1 channels" [FEBS Lett. 580 (2006) 5728-5732]. FEBS Lett. 581(8): 1699. dx.doi.org/10.1016/j.febslet.2007.03.036, meer
Cuypers, E.; Yanagihara, A.; Karlsson, E.; Tytgat, J. (2006). Jellyfish and other cnidarian envenomations cause pain by affecting TRPV1 channels. FEBS Lett. 580(24): 5728-5732. dx.doi.org/10.1016/j.febslet.2006.09.030, meer
Kauferstein, S.; Huys, I.; Kuch, U.; Melaun, C.; Tytgat, J.; Mebs, D. (2004). Novel conopeptides of the I-superfamily occur in several clades of cone snails. Toxicon 44(5): 539-548, meer
Fan, C.X.; Chen, X.K.; Zhang, C.; Wang, L.X.; Duan, K.L.; He, L.L.; Cao, Y.; Liu, S.Y.; Zhong, M.N.; Ulens, C.; Tytgat, J.; Chen, J.S.; Chi, C.W.; Zhou, Z. (2003). A novel conotoxin from Conus betulinus, kappa-BtX, unique in cysteine pattern and in function as a specific BK channel modulator. J. Biol. Chem. 278(15): 12624-12633. https://dx.doi.org/10.1074/jbc.M210200200, meer
Bosmans, F.; Aneiros, A.; Tytgat, J. (2002). The sea anemone Bunodosoma granulifera contains surprisingly efficacious and potent insect-selective toxins. FEBS Lett. 532(1-2): 131-134. dx.doi.org/10.1016/S0014-5793(02)03653-0, meer
Goudet, C.; Ferrero, T.; Galàn, L.; Artiles, A.; Batista, C.F.V.; Possani, L.D.; Alvarez, J.; Aneiros, A.; Tytgat, J. (2001). Characterization of two Bunodosoma granulifera toxins active on cardiac sodium channels. Br. J. Pharmacol. 134(6): 1195-1206. dx.doi.org/10.1038/sj.bjp.0704361, meer
- De Raedemaecker, F.; Sandra, M.; Devriese, L; Goeminne, G.; Bicalho, K.; Montoye, T.; Tytgat, J.; Bernaerts, H.; Coenye, T.; Van Vlierberghe, W.; Loosvelt , L. (2021). Prospection for bioactive compounds in the North Sea: Creating a knowledge base for blue biotech innovation in Flanders, in: Mees, J. et al. Book of abstracts – VLIZ Marine Science Day, Online event 3 March 2021. VLIZ Special Publication, 87: pp. 45, meer
- De Raedemaecker, F.; Sandra, M.; Devriese, L.I.; Goeminne, G.; Bicalho, K.; Montoye, T.; Tytgat, J.; Bernaerts, H.; Loosvelt , L. (2021). PROspectionfor BIOactivecompounds in the North Sea (PROBIO): creating a knowledge base for blue biotech innovation in Flanders. Poster submited at VLIZ Marine Science Day, Online event 3 March 2021. VLIZ/KU Leuven/Universiteit Gent: Oostende. 1 poster pp., meer
- Tytgat, J. (2017). α-Nemertides, a novel family of marine peptide neurotoxins from ribbon worms. KULeuven: Leuven. , meer
- Kopljar, I.; Peigneur, S.; Snyders, D.J.; Tytgat, J. (2014). The mechanism of action of microalgal toxins interacting with Nav and Kv channels, in: Rossini, G.P. (Ed.) Toxins and biologically active compounds from microalgae: Volume 2. Biological effects and risk management. pp. 3-34, meer
- Peigneur, S.; Béress, L.; Möller, C.; Marí, F.; Forssmann, W.-G.; Tytgat, J. (2013). Sea anemone toxins: insecticides and painkillers of the future?, in: Mees, J. et al. (Ed.) Marine biotechnology in the European research area: Challenges and opportunities for Europe. Final CSA MarineBiotech Conference. Royal Flemish Academy of Belgium for Science and the Arts, Brussels, Belgium, 11-12 March 2013. VLIZ Special Publication, 64: pp. 7, meer
- Tytgat, J. (2009). Expectancies of a toxicologist: from sudden poisoning to miraculous discovery, in: Mees, J. et al. (Ed.) VLIZ Young Scientists' Day, Brugge, Belgium 6 March 2009: book of abstracts. VLIZ Special Publication, 41: pp. 14, meer
- Tytgat, J. (2008). Toxines van kwallen en zeeanemonen (Cnidaria): een ‘zee’ van moleculen geschikt voor de ontwikkeling van nieuwe geneesmiddelen. Prijs Dr. E. Delcroix 2007 - 11 april 2008, Oostende. [S.n.]: [s.l.]. 1 presentation [52 Slides] pp., meer
- Tytgat, J. (2007). Toxines van kwallen en zeeanemonen (Cnidaria): een ‘zee’ van moleculen geschikt voor de ontwikkeling van nieuwe geneesmiddelen. Katholieke Universiteit Leuven. Faculteit Farmaceutische Wetenschappen. Laboratorium Toxicologie: Leuven. 23 pp., meer
- Tytgat, J. (2007). Toxins from jellyfish and sea anemones: a 'sea' of molecules with therapeutic potential. KU Leuven, Laboratorium Toxicologie: Leuven. 23 pp., meer
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- Kick-off PROBIO: PROspection for BIOactive compounds in the North Sea
- PROBIO meeting - PROspection for BIOactive compounds in the North Sea
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