Heteroscodratoxin-1

Heteroscodratoxin-1 (also known as κ-theraphototoxin-Hm1a, κ-TRTX-Hm1a, δ-theraphotoxin-Hm1a, δ-TRTX-Hm1a, Hm1a or HmTx1) is a neurotoxin produced by the venom glands of Heteroscodra maculata (Togo starburst tarantula)[1] that shifts the activation threshold of voltage-gated potassium channels and the inactivation of Nav1.1 sodium channels to more positive potentials.[2][3]

Heteroscodratoxin-1
Schematic diagram of the three-dimensional structure of Heteroscodratoxin-1.
Identifiers
OrganismHeteroscodra maculata
SymbolN/A
UniProtP60992
Search for
StructuresSwiss-model
DomainsInterPro

Sources

Heteroscodratoxin-1 can be obtained from venom glands of Heteroscodra maculata (Togo starburst tarantula or Togo starburst baboon spider).[2]

Chemistry

Heteroscodratoxin-1 is a basic protein (isoelectric point of 7.7) composed of 35 amino acids with a carboxylated C-terminus. Its sequence shows strong similarity with other tarantula toxins such as scodratoxin, hanatoxin and SGTx1. Structurally the protein belongs to the huwentoxin-1 family of inhibitory spider peptides based on its knottin backbone that consists of three crossing disulfide bridges (Cys1-Cys4/Cys2-Cys5/Cys3-Cys6).[2] Hm1a has the following amino acid sequence: ECRYLFGGCSSTSDCCKHLSCRSDWKYCAWDGTFS. Its molecular weight is 3,995.61 Da.[3]

Target

Heteroscodratoxin-1 inhibits subtypes of both delayed rectifier (KV2.1 and KV2.2) and A-type rapidly inactivating (KV4.1, KV4.2 and KV4.3) voltage-gated potassium channels. At a concentration of 100-300 nM, in transfected COS cells it blocks 23% of KV2.1, 19% of KV2.2, 50% of KV4.1, 39% of KV4.2, and 43% of KV4.3 conductance at a potential of 0 mV. No significant effect on other A-type rapidly inactivating (KV1.4 and KV3.4) or delayed rectifier potassium channels (KV1.1, KV1.2, KV1.3, KV1.5, KV1.6, KV1.2/ KV1.5, or KVLQT1), or on sodium and calcium channels has been observed.[2]

Physiologically probably more important than its action on potassium channels is its action on the voltage-gated sodium channel Nav1.1 (EC50 = 38 ± 6 nM). More specifically, it is thought that Hm1a targets the domain IV S3-S4 loop and the S1-S2 loop of Nav1.1, as application of this toxin to a chimeric channel which contained these regions resulted in full toxin sensitivity (compared to other chimeric channels which contained only one of either of these regions). This, therefore, indicates that both the S1-S2 and the S3-S4 domains determine toxin sensitivity and selectivity.[3]

Hm1a enhances the Nav1.1 channel activity by inhibiting fast and slow inactivation of the channel. Hm1a prevents the movement of the voltage sensor domain IV. Hm1a and Hm1b prevent the movement of the sensor domain towards the inner part of the cell thereby inhibiting fast inactivation of the Nav1.1 channel. Hm1a also inhibits the slow inactivation of the Nav1.1 channel by preventing a current reduction in the ion channel, but the underlying mechanism has not yet been elucidated.[4]

Mode of action

It is thought that heteroscodratoxin-1 modifies gating of specific potassium channels by shifting the activation threshold to more positive values. As a result larger depolarizations are needed to open channels. The mechanism underlying this modification has been largely elucidated using molecular docking simulation for the KV2.1 potassium channel which is highly expressed in mammalian neurons and interacts strongly with heteroscodratoxin-1. In this model the C-terminal residue of the KV2.1 S3-segment (S3C) serves as a binding site for Hmtx-1 forming both hydrophobic and hydrophilic bonds. Interaction between the toxin and the potassium channel induces a helical movement of S3C resulting in limited spatial freedom of the S4-segment which is responsible for channel gating.[5]

Toxicity

Information on toxic effects of Heteroscodratoxin-1 in humans is not available. In mice, however, it has been found that intracerebroventricular injection of 500 pmol HmTx1 induces convulsions, spasms, tremors and death within 1 hour. At 100 pmol, a less severe response develops, although death still occurs after 2 hours.[2]

References
  1. "Kappa-theraphotoxin-Hm1a - Heteroscodra maculata (Togo starburst tarantula)". Uniprot.org. 2011-09-21. Retrieved 2011-10-08.
  2. Escoubas P, Diochot S, Célérier ML, Nakajima T, Lazdunski M (July 2002). "Novel tarantula toxins for subtypes of voltage-dependent potassium channels in the Kv2 and Kv4 subfamilies". Molecular Pharmacology. 62 (1): 48–57. doi:10.1124/mol.62.1.48. PMID 12065754.
  3. Osteen, Jeremiah D.; Herzig, Volker; Gilchrist, John; Emrick, Joshua J.; Zhang, Chuchu; Wang, Xidao; Castro, Joel; Garcia-Caraballo, Sonia; Grundy, Luke (June 2016). "Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain". Nature. 534 (7608): 494–499. Bibcode:2016Natur.534..494O. doi:10.1038/nature17976. ISSN 0028-0836. PMC 4919188. PMID 27281198.
  4. Osteen, Jeremiah D.; Sampson, Kevin; Iyer, Vivek; Julius, David; Bosmans, Frank (2017-06-12). "Pharmacology of the Nav1.1 domain IV voltage sensor reveals coupling between inactivation gating processes". Proceedings of the National Academy of Sciences. 114 (26): 6836–6841. doi:10.1073/pnas.1621263114. ISSN 0027-8424. PMC 5495237. PMID 28607094.
  5. Shiau YS, Huang PT, Liou HH, Liaw YC, Shiau YY, Lou KL (October 2003). "Structural basis of binding and inhibition of novel tarantula toxins in mammalian voltage-dependent potassium channels". Chemical Research in Toxicology. 16 (10): 1217–25. doi:10.1021/tx0341097. PMID 14565763.
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