Mipartoxin-I is a neurotoxin produced by Micrurus mipartitus , a venomous coral snake distributed in Central and South America. This toxin causes a neuromuscular blockade by blocking the nicotinic acetylcholine receptor. It is the most abundant component in the venom. [1]
The toxin is produced by the Micrurus mipartitus, also known as the ‘redtail coral snake’, ‘rabo de ají’, or ‘gargantilla’. [2] The snake populates Nicaragua, Costa Rica, isthmus of Panama, Ecuador, Colombia, Venezuela and Brazil.
Mipartoxin-I is a short-chain, type-I, α-neurotoxin composed of 60 amino acids with a molecular mass of 7030 Da. [2] It is a member of the three finger toxin (3FTx) superfamily, and it contains the characteristic eight cysteines of this superfamily.
CTX A5, a cardiotoxin from the cobra Najaatra, shows similarities with mipartoxin-I in the predicted core region and in amino acid sequence identity (38%). However, there are some slight differences in loop 1 and 2, and major differences in loop 3. [2] Mipartoxin-I generally shows relatively low sequence similarity with other 3FTx family members.
Mipartoxin-I is proposed to bind antagonistically to the nicotinic acetylcholine receptors and consequently inhibit the activity of this receptor without damaging the muscle fibres. [3] The toxin blocks the muscle contractions without interfering with presynaptic acetylcholine release, indicating that it acts post-synaptically. [2] [4]
Envenoming mice with Mipartoxin-I causes bilateral ptosis and progressive respiratory paralysis. Following a decrease in activity and respiratory paralysis, mice die a few hours after envenoming. The LD50 of mipartoxin-I is 0.06 μg/g body weight. [2] [3]
Currently, no specific antivenom is available in most of its important geographic field (Central America). The scarcity of an antivenom is complicated by insufficient cross-protection by antivenoms that are more accessible in this geographic area. However, the similarity in amino acid sequence of related toxins of two South American coral snakes were high (M.frontalis 70% and M.altirostris 68%). This indicates a possible cross-protection of these two antivenoms for mipartoxin-I. [2]
Mambas are fast-moving, highly venomous snakes of the genus Dendroaspis in the family Elapidae. Four extant species are recognised currently; three of those four species are essentially arboreal and green in colour, whereas the black mamba, Dendroaspis polylepis, is largely terrestrial and generally brown or grey in colour. All are native to various regions in sub-Saharan Africa and all are feared throughout their ranges, especially the black mamba. In Africa there are many legends and stories about mambas.
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Naja is a genus of venomous elapid snakes commonly known as cobras. Members of the genus Naja are the most widespread and the most widely recognized as "true" cobras. Various species occur in regions throughout Africa, Southwest Asia, South Asia, and Southeast Asia. Several other elapid species are also called "cobras", such as the king cobra and the rinkhals, but neither is a true cobra, in that they do not belong to the genus Naja, but instead each belong to monotypic genera Hemachatus and Ophiophagus.
Delta atracotoxin is a low-molecular-weight neurotoxic polypeptide found in the venom of the Sydney funnel-web spider.
α-Bungarotoxin is one of the bungarotoxins, components of the venom of the elapid Taiwanese banded krait snake. It is a type of α-neurotoxin, a neurotoxic protein that is known to bind competitively and in a relatively irreversible manner to the nicotinic acetylcholine receptor found at the neuromuscular junction, causing paralysis, respiratory failure, and death in the victim. It has also been shown to play an antagonistic role in the binding of the α7 nicotinic acetylcholine receptor in the brain, and as such has numerous applications in neuroscience research.
Taipoxin is a potent myo- and neurotoxin that was isolated from the venom of the coastal taipan Oxyuranus scutellatus or also known as the common taipan. Taipoxin like many other pre-synaptic neurotoxins are phospholipase A2 (PLA2) toxins, which inhibit/complete block the release of the motor transmitter acetylcholine and lead to death by paralysis of the respiratory muscles (asphyxia). It is the most lethal neurotoxin isolated from any snake venom to date.
β-Bungarotoxin is a form of bungarotoxin that is fairly common in Krait venoms. It is the prototypic class of snake β-neurotoxins. There are at least five isoforms, coded β1 to β5, assembled from different combinations of A and Bchains.
Micrurus corallinus is a species of highly venomous elapid snake native to South America. There are no recognized subspecies.
α-Neurotoxins are a group of neurotoxic peptides found in the venom of snakes in the families Elapidae and Hydrophiidae. They can cause paralysis, respiratory failure, and death. Members of the three-finger toxin protein family, they are antagonists of post-synaptic nicotinic acetylcholine receptors (nAChRs) in the neuromuscular synapse that bind competitively and irreversibly, preventing synaptic acetylcholine (ACh) from opening the ion channel. Over 100 α-neurotoxins have been identified and sequenced.
Mambalgins are peptides found in the venom of the black mamba, an elapid snake. Mambalgins are members of the three-finger toxin (3FTx) protein family and have the characteristic three-finger protein fold. First reported by French researchers in 2012, mambalgins are unusual members of the 3FTx family in that they have the in vivo effect of causing analgesia without apparent toxicity. Their mechanism of action is potent inhibition of acid-sensing ion channels.
κ-Bungarotoxin is a protein neurotoxin of the bungarotoxin family that is found in the venom of the many-banded krait, a snake found in Taiwan. κ-Bungarotoxin is a high affinity antagonist of nicotinic acetylcholine receptors (nAChRs), particularly of CHRNA3; it causes a post-synaptic blockade of neurotransmission. Although there is significant variability in the clinical effects of snake bites, neuromuscular paralysis and respiratory failure are associated with krait bites.
Micrurus frontalis, also known as the southern coral snake or short-tailed coral snake, is a species of highly venomous coral snake in the family Elapidae. It is found in South America.
Micrurus mipartitus is a species of coral snake in the family Elapidae. The species is native to Central America and northern South America. The red-tailed coral snake is common in agricultural areas in Colombia. Its highly neurotoxic venom is known to cause seizures in its prey by activating nerve proteins responsible for seizures within it.
Three-finger toxins are a protein superfamily of small toxin proteins found in the venom of snakes. Three-finger toxins are in turn members of a larger superfamily of three-finger protein domains which includes non-toxic proteins that share a similar protein fold. The group is named for its common structure consisting of three beta strand loops connected to a central core containing four conserved disulfide bonds. The 3FP protein domain has no enzymatic activity and is typically between 60-74 amino acid residues long. Despite their conserved structure, three-finger toxin proteins have a wide range of pharmacological effects. Most members of the family are neurotoxins that act on cholinergic intercellular signaling; the alpha-neurotoxin family interacts with muscle nicotinic acetylcholine receptors (nAChRs), the kappa-bungarotoxin family with neuronal nAChRs, and muscarinic toxins with muscarinic acetylcholine receptors (mAChRs).
Three-finger proteins or three-finger protein domains are a protein superfamily consisting of small, roughly 60-80 amino acid residue protein domains with a common tertiary structure: three beta strand loops extended from a hydrophobic core stabilized by disulfide bonds. The family is named for the outstretched "fingers" of the three loops. Members of the family have no enzymatic activity, but are capable of forming protein-protein interactions with high specificity and affinity. The founding members of the family, also the best characterized by structure, are the three-finger toxins found in snake venom, which have a variety of pharmacological effects, most typically by disruption of cholinergic signaling. The family is also represented in non-toxic proteins, which have a wide taxonomic distribution; 3FP domains occur in the extracellular domains of some cell-surface receptors as well as in GPI-anchored and secreted globular proteins, usually involved in signaling.
Long neurotoxin 1 (LNTX-1) is a neurotoxin that binds antagonistically to all types of muscular and neuronal nicotinic acetylcholine receptors. LNTX-1 is found in the venom of the king cobra.
Crotoxin (CTX) is the main toxic compound in the snake venom of the South American rattlesnake, Crotalus durissus terrificus. Crotoxin is a heterodimeric beta-neurotoxin, composed of an acidic, non-toxic and non-enzymatic subunit (CA), and a basic, weakly toxic, phospholipase A2 protein (CB). This neurotoxin causes paralysis by both pre- and postsynaptic blocking of acetylcholine signalling.
Notexin is a toxin produced by the tiger snake (Notechis scutatus). It is a myotoxic and presynaptic, neurotoxic phospholipase A2 (PLA2s). These are enzymes that hydrolyze the bond between a fatty acid tail and glycerol in fatty acids on the 2-position.
MiDCA1, short for Micrurus dumerili carinicauda 1, is a β-neurotoxin primarily affecting presynaptic synapses, where it interferes with the release of neurotransmitters by inhibiting potassium (K+) channels. This toxin belongs to the phospholipase A2 (PLA2) family but distinguishes itself by existing as a monomer, unlike some other PLA2 toxins. It occurs naturally in the venom of the coral snake Micrurus dumerili carinicauda.