Pseudonajatoxin b, or Pt-b, is a highly potent and lethal long-chain α-neurotoxin found in the venom of the eastern brown snake (Pseudonaja textilis). While the pharmacodynamics of pseudonajatoxin b are currently undocumented, α-neurotoxins are known to cause neuromuscular paralysis by blocking cholinergic neurotransmission.
Source
editPseudonajatoxin b is present in the venom of the highly lethal eastern brown snake, Pseudonaja textilis,[1][2] which is the leading cause of snakebites in Australia.[3] The concentration of pseudonajatoxin b in venom of South Australian specimens is up to a hundred times higher than in those from Queensland.[2]
Chemistry
editStructure and homology
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Pseudonajatoxin b is composed of a single polypeptide chain of 71 amino acids and features five disulphide bridges. It exhibits 61-73% sequence homology with other long neurotoxins. Distinctive characteristics of pseudonajatoxin b include a high occurrence of proline residues, particularly at positions 49 and 54, where valines are usually present. Moreover, it contains an additional amino acid in the loop between Cys-46 and Cys-58.[5]
Protein family
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Pseudonajatoxin b is a type of three-finger toxin, which are characterized by a structure of three loops that emerge from a hydrophobic core.[3] Specifically, it falls within the long-chain subfamily of the α-neurotoxin group.[5]
Target and mechanism of action
editAlthough the pharmacodynamics of pseudonajatoxin b have not been documented, α-neurotoxins generally exhibit some common traits.
Long-chain α-neurotoxins have been shown to bind with high affinity to both muscular and neuronal nicotinic acetylcholine receptors.[2][6][7] These receptors serve as the primary mediator of muscle contraction in response to nerve impulses. Additionally, they are present in the central nervous system, where they play an important role in autonomic processes, including the regulation of heart rate and respiration.
By acting as competitive antagonists to acetylcholine, α-neurotoxins block acetylcholine from binding and subsequently prevent the activation of ion channels.[7] This disruption in neurotransmission effectively leads to neuromuscular paralysis.[8] Importantly, since the activation of nicotinic acetylcholine receptors requires the binding of two acetylcholine molecules, the blockage of just one binding site by an α-neurotoxin is sufficient to prevent channel opening.[9] Furthermore, long-chain α-neurotoxins typically bind tightly and irreversibly to nicotinic receptors, resulting in permanent channel inactivation once they are bound.[5][10]
Toxicity and treatment
editPseudonajatoxin b is a highly potent toxin, with a median lethal dose (LD50) of 15 pg/kg in mice.[5] Although the specific lethal mechanisms of pseudonajatoxin b remain unknown, it is well established that both α-neurotoxins and the venom of P. textilis induce paralysis, leading to death through asphyxiation.[7][8]
Currently, no treatment specific for pseudonajatoxin b has been documented. However, envenomation from Pseudonaja textilis can be treated with snake antivenom made from antibodies, specifically horse immuno-globulins.[3] Despite this, studies have shown that brown snake antivenom has low efficacy against Pseudonaja textilis venom.[3]
References
edit- ^ Viala, Vincent Louis; Hildebrand, Diana; Trusch, Maria; Fucase, Tamara Mieco; Sciani, Juliana Mozer; Pimenta, Daniel Carvalho; Arni, Raghuvir K.; Schlüter, Hartmut; Betzel, Christian; Mirtschin, Peter; Dunstan, Nathan; Spencer, Patrick Jack (2015-12-01). "Venomics of the Australian eastern brown snake (Pseudonaja textilis): Detection of new venom proteins and splicing variants". Toxicon. Omic perspectives of the toxin universe. 107 (Pt B): 252–265. Bibcode:2015Txcn..107..252V. doi:10.1016/j.toxicon.2015.06.005. ISSN 0041-0101. PMID 26079951.
- ^ a b c Skejic, Jure; Steer, David L.; Dunstan, Nathan; Hodgson, Wayne C. (2015-11-06). "Label-Free (XIC) Quantification of Venom Procoagulant and Neurotoxin Expression in Related Australian Elapid Snakes Gives Insight into Venom Toxicity Evolution". Journal of Proteome Research. 14 (11): 4896–4906. doi:10.1021/acs.jproteome.5b00764. ISSN 1535-3893. PMID 26486890.
- ^ a b c d Viala, Vincent Louis; Hildebrand, Diana; Trusch, Maria; Fucase, Tamara Mieco; Sciani, Juliana Mozer; Pimenta, Daniel Carvalho; Arni, Raghuvir K.; Schlüter, Hartmut; Betzel, Christian; Mirtschin, Peter; Dunstan, Nathan; Spencer, Patrick Jack (2015-12-01). "Venomics of the Australian eastern brown snake (Pseudonaja textilis): Detection of new venom proteins and splicing variants". Toxicon. Omic perspectives of the toxin universe. 107 (Pt B): 252–265. Bibcode:2015Txcn..107..252V. doi:10.1016/j.toxicon.2015.06.005. ISSN 0041-0101. PMID 26079951.
- ^ a b "UniProt". www.uniprot.org. Retrieved 2024-10-21.
- ^ a b c d Tyler, Margaret I.; Howden, Merlin E. H.; Spence, Ian; Barnett, Donald (July 1987). "Pseudonajatoxin b: unusual amino acid sequence of a lethal neurotoxin from the venom of the Australian common brown snake, Pseudonaja textilis". European Journal of Biochemistry. 166 (1): 139–143. doi:10.1111/j.1432-1033.1987.tb13493.x. ISSN 0014-2956. PMID 3595609.
- ^ Endo, Toshiya; Tamiya, Nubuo (1987-01-01). "Current view on the structure-function relationship of postsynaptic neurotoxins from snake venoms". Pharmacology & Therapeutics. 34 (3): 403–406. doi:10.1016/0163-7258(87)90002-7. ISSN 0163-7258. PMID 3324114.
- ^ a b c Phui Yee, Joyce Siew; Nanling, Gong; Afifiyan, Fatemah; Donghui, Ma; Siew Lay, Poh; Armugam, Arunmozhiarasi; Jeyaseelan, Kandiah (2004-02-01). "Snake postsynaptic neurotoxins: gene structure, phylogeny and applications in research and therapy". Biochimie. 86 (2): 137–149. doi:10.1016/j.biochi.2003.11.012. ISSN 0300-9084. PMID 15016453.
- ^ a b St Pierre, L.; Fischer, H.; Adams, D. J.; Schenning, M.; Lavidis, N.; de Jersey, J.; Masci, P. P.; Lavin, M. F. (2007-11-01). "Distinct activities of novel neurotoxins from Australian venomous snakes for nicotinic acetylcholine receptors". Cellular and Molecular Life Sciences. 64 (21): 2829–2840. doi:10.1007/s00018-007-7352-z. ISSN 1420-9071. PMC 11136185. PMID 17906946.
- ^ Sine, S. M.; Taylor, P. (1981-07-10). "Relationship between reversible antagonist occupancy and the functional capacity of the acetylcholine receptor". The Journal of Biological Chemistry. 256 (13): 6692–6699. doi:10.1016/S0021-9258(19)69047-2. ISSN 0021-9258. PMID 7240238.
- ^ Tipton, Keith F.; Dajas, Federico, eds. (1994). Neurotoxins in neurobiology: their actions and applications. Ellis Horwood series in neuroscience (1. publ ed.). New York: Ellis Horwood. ISBN 978-0-13-614991-0.