Part:BBa_K5184033
HxTx-Hv1h
In order to eliminate spider mites, spider venom peptide HxTx-Hv1h is incorporated in our project to broaden the spectrum of molecular targets of venom peptides. HxTx-Hv1h is a small cysteine-rich venom peptide derived from Hadronyche versuta. Utilized as predatory toxin in nature, it carries the ability to cause paralysis and death in susceptible subjects by interfering with voltage-gated calcium and potassium channels. Given CaV and KV channels' roles in neurotransmitter release and neural impulse relay, HxTx-Hv1h serves as an effective pesticide.
Sequences
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
HxTx-Hv1h is a 39aa long peptide containing 6 cysteine residues arranged to create a cysteine framework of C1xxxC2xxxC3C4xxxC5xxxC6, forming cysteine cross bridges between C1C4, C2C6, and between C3C5 [Fig1A].
Paralysis and mortal effects of susceptible subjects are achieved via HxTx-Hv1h inhibition on both CaV and KCa channels of susceptible targets by blocking the channels directly, resulting in impediment of fundamental nervous system responses in neuronal, muscular, and cardiac functions. (Specific site of inhibition depends on the concentration of neurotoxin).
Toxicity Verification
HxTx-Hv1h is synthesized using the vector pET28a-G1M5-His-SUMO-HxTx-Hv1h-GNA-His[Fig2B], of which is assembled using GoldenGate cloning and transformed into E. coli strain DH5ɑ. Colony PCR and sequencing is then carried out to verify the plasmid construct, of which is extracted and transformed into BL21(DE3) strain for expression. After IPTG induction and overnight incubation, the liquid culture is harvested and, after cell lysis, have an SDS-PAGE run. The results suggest that HxTx-Hv1h had achieved soluble expression. After several unsuccessful purification attempts, the supernatant is treated directly by SUMO protease [Fig2C].
The SUMO-digested supernatant's toxicity against T. urticae females is tested using a spraying method by Professor Huang from SCAU. Results from the toxicity assay suggests HxTx-Hv1h to be highly toxic against T. urticae, achieving an fatality of 90.91% within 72 hours.
Part Collection
Our part collection provides a comprehensive list of venom peptides with a diverse range of molecular targets, and all displays satisfactory elimination efficacy during our testings [Fig7A&B].
Current VP | Venom Name | Targeted Ion Channel | New? | Part Number | Original Specie |
---|---|---|---|---|---|
PpVP2S | Ca | New | BBa_K5184043 | Phytoseiulus persimilis | |
PpVP1S | Ca | New | BBa_K5184042 | Phytoseiulus persimilis | |
PpVP1F | Ca | New | BBa_K5184038 | Phytoseiulus persimilis | |
rCtx4 | Na | BBa_K5184021 | Phoneutria depilata | ||
Cs1A | Ca | BBa_K5184032 | Calommata signata | ||
✳️ | HxTx-Hv1h | Ca, K | BBa_K5184033 | Hadronyche versuta |
None |