Hainantoxin
Hainantoxins are neurotoxins from the venom of the Chinese bird spider Cyriopagopus hainanus. Hainantoxins specifically inhibit tetrodotoxin-sensitive Voltage-gated sodium channels, thereby causing blockage of neuromuscular transmission and paralysis. Currently, 13 different hainantoxins are known, but only HNTX-I, -II, -III, -IV and -V have been investigated in detail.
Chemistry
Structure
Hainantoxins I, III, IV and V show high homology, including the presence of three disulfide bonds that form an inhibitor cysteine knot motif.HNTX-I
The main component of the venom of O. hainana is HNTX-I. It has 33 amino acid residues, with a total molecular weight of 3605-3608 Da. HNTX-I contains a short triple-stranded anti-parallel beta-sheet and four beta-turns. The amino acid residues His28 and Asp26 are needed for the bioactivity of HNTX-I.HNTX-II
HNTX-II has a molecular weight of 4253 Da and contains 37 amino acid residues. The complete amino acid sequence of HNTX-II is NH2-LFECSV SCEIEK EGNKD CKKKK CKGGW KCKFN MCVKV-COOH.HNTX-III
The structure of HNTX-III consists of 33-35 amino acid residues, which form a beta-sheet with connections between Asp7 and Cys9, Tyr21 and Ser23, and Lys27 and Val30.HNTX-IV
HNTX-IV has 35 amino acid residues with a total molecular weight of 3989 Da. The first strand consists of an antiparallel beta-sheet. The complete amino acid sequence of HNTX-IV is NH2-ECLGFG KGCNPS NDQCCK SSNLVC SRKHRW CKYEI-CONH2. Lys 27, His28, Arg29 and Lys 32 are the neuroactive amino acid residues.HNTX-V
HNTX-V consists of 35 amino acid residues. The whole amino acid residue sequence of HNTX-V is NH2-ECLGFG KGCNPS NDQCCK SANLVC SRKHRW CKYEI-COOH. At the active binding site of HNTX-V, Lys27 and Arg 29 are the most important.Target
Channel
Hainantoxins selectively inhibit tetrodotoxin-sensitive voltage-gated sodium channels. Voltage-gated Ca2+ channels, tetrodotoxin-resistant VGSCs and rectifier-delayed potassium channels are not affected. HNTX-III and HNTX-IV are part of the Huwentoxin-I family. Toxins from the Huwentoxin-I family are thought to bind to site 1 on the sodium channels. Other hainantoxins bind at site 3 of the sodium channels. HNTX-I specifically blocks mammalian Nav1.2 and insect para/tipE channels expressed in Xenopus laevis oocytes. HNTX-I is a weak antagonist of the vertebrate TTX-S VGSCs, but is more potent on insect VGSCs.Affinity
For the blockage of sodium channels, electrostatic interactions or hydrogen bonds are needed. Important for the electrostatic interaction is the presence of a positively charged region in the toxin, because the receptor site of the sodium channel contains a lot of negatively charged residues. In HNTX-I, the positively charged residues and a vicinal hydrophobic patch have most influence on the binding to the sodium channels. HNTX-IV has a positively charged patch containing the amino acids Arg26, Lys27, His28, Arg29 and Lys32, of which Lys27, Arg29 and Lys32 are the most important for interaction with the TTX-S VGSCs. HNTX-V also shows an interface of positively charged amino acids that are responsible for the binding with the TTX-S VGSCs, where also Lys27 and Arg29 are the most important. Subtle differences in the positively charged patch can result in altered electrostatic properties, causing altered pharmacological effects.Table 1: IC50 values of four subgroups of hainantoxins
| IC50 | |
| HNTX-I | 68 μM |
| HNTX-III | 1.1 nM |
| HNTX-IV | 44.6 nM |
| HNTX-V | 42.3 nM |