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BmKAEP

From Wikipedia, the free encyclopedia

BmKAEP (or anti-epilepsy peptide) is a neurotoxin from the venom of the Manchurian scorpion (Mesobuthus martensii). It is a β-toxin, which shift the activation voltage of sodium channels towards more negative potentials.

Etymology

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BmK is the abbreviation for Buthus martensi Karsch, an old name for the scorpion that is the source of BmKAEP; AEP is an abbreviation for anti-epilepsy peptide. At the NCBI Protein Database, the full name of this peptide is listed as "Toxin BmKAEP".[1]

Sources

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Manchurian scorpion (Mesobuthus martensii)

BmKAEP is one of the components of Mesobuthus martensii's venom,[2] a well-known scorpion belonging to the family Buthidae, which is found distributed throughout Eastern Asia and China.

Chemistry

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BmKAEP is an inhibitory β-toxin and thus, a Na+ channel inhibitor. As with other mammal and insect toxins, BmKAEP is classified according to species and mechanism of action.[3]

BmKAEP is a 61-amino-acid protein derived from an 85-amino-acid precursor. The mature protein contains 8 cysteine residues that establish 4 disulfide bridges (4C-C).[3] Despite its high homology with other depressant toxins, BmKAEP differs from them at residues 6, 7 and 39, which is thought to be important in determining its unique function.[3] Its lysine residue, at position 51, also has a special feature: it interacts with mammalian Na+ channels.[4]

BmKAEP primary sequence[5]

01 mklflllvis asmlidglvn adgyirgsng
31 ckvsclwgne gcnkeckafg ayygycwtwg
61 lacwceglpd dktwksesnt cggkk

Target and Mode of Action

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Because of its sequence homology with other β-toxins, BmKAEP is predicted to bind to site 4 (S4) of voltage-gated Na+ channels, at domains I, III and IV.[6] Its interaction with the S4 loop causes the loop to be maintained at the outward activated position. Therefore, activation of the Na+ channels shifts towards more negative values,[7] enhancing the channel's activation and promoting spontaneous and repetitive firing. Subsequently, the sodium current amplitude decreases, due to the membrane potential depolarization, thus suppressing action potentials.[2]

Toxicity

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BmK venom induces a transient phase of contraction followed by a slow progressive flaccid paralysis in insect larvae.[8] However, since it requires a high dosage to be effective, its toxicity is weak, both in insects and mammals.[9]

Toxicity parameters
LD50 2,4 mg/kg (mice; intraperitoneal injection)[3]
MLD (minimum lethal dose) 0,074 mg/kg (mice; Intracerebroventricular injection)[2]
CPU (concentration paralysis unit) 1 μg/body (larvae)[2]
NOAEL (No observed adverse effect) <2 μg (insects); <20 μg (mice)[3]

Therapeutic use

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Though the exact mechanism of its anti-epilepsy effect is not clear, several studies have shown that BmKAEP can inhibit coriaria lactone-induced epilepsy in rats by prolonging the latent epilepsy period, relieving the degree of seizures and shortening its average duration, at a pharmacological dosage of only 0.057 μg/g.[9]

Mesobuthus martensii, especially its tail, has been used in Chinese traditional medicine to treat several neuronal diseases, such as several types of paralysis, apoplexy and epilepsy.[2]

References

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  1. ^ "Toxin BmKAEP". NCBI. Retrieved 25 October 2010.
  2. ^ a b c d e doi:10.1016/S0041-0101(02)00142-3. PMID 12220709.
  3. ^ a b c d e Wang CG, He XL, Shao F, Liu W, Ling MH, Wang DC, Chi CW (April 2001). "Molecular characterization of an anti-epilepsy peptide from the scorpion Buthus martensi Karsch". European Journal of Biochemistry. 268 (8): 2480–5. doi:10.1046/j.1432-1327.2001.02132.x. PMID 11298767.
  4. ^ doi:10.1016/j.toxicon.2010.02.019. PMID 20219516.
  5. ^ Universal protein resource accession number P15228 for "Toxin BmKAEP" at UniProt.
  6. ^ Cestèle S, Catterall WA (2000). "Molecular mechanisms of neurotoxin action on voltage-gated sodium channels". Biochimie. 82 (9–10): 883–92. doi:10.1016/S0300-9084(00)01174-3. PMID 11086218.
  7. ^ Cestèle S, Qu Y, Rogers JC, Rochat H, Scheuer T, Catterall WA (October 1998). "Voltage sensor-trapping: enhanced activation of sodium channels by beta-scorpion toxin bound to the S3-S4 loop in domain II". Neuron. 21 (4): 919–31. doi:10.1016/S0896-6273(00)80606-6. PMID 9808476.
  8. ^ doi:10.1016/S0041-0101(98)00160-3. PMID 9792184.
  9. ^ a b Zhou XH, Yang D, Zhang JH, Liu CM, Lei KJ (January 1989). "Purification and N-terminal partial sequence of anti-epilepsy peptide from venom of the scorpion Buthus martensii Karsch". The Biochemical Journal. 257 (2): 509–17. doi:10.1042/bj2570509. PMC 1135608. PMID 2930463.
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