Mu-theraphotoxin-Pspp1 | |||||||
---|---|---|---|---|---|---|---|
Identifiers | |||||||
Organism | Phlogiellus sp. (Tarantula) | ||||||
Symbol | PhlTx1 | ||||||
UniProt | P0DM14 | ||||||
|
Phlotoxin (PhlTx1, μ-TRTX-Pspp-1) is a neurotoxin from the venom of the tarantula Phlogiellus that targets mostly voltage-sensitive sodium channels and mainly Nav1.7. The only non-sodium voltage-sensitive channel that is inhibited by Phlotoxin is Kv3.4. Nav1.4 and Nav1.6 seem to be Phlotoxin-1-sensitive to some extent as well.
Phlotoxin (μ-TRTX-Pspp-1) | |
Category | Ion channel toxin, Neurotoxin |
---|---|
Genus | Phlogiellus |
Target | voltage-gated sodium channel (mainly) |
Spider toxin family | NaSpTx-1 |
Sequence length | 34 amino acids with 3 disulfide bridges |
Mass | 4058.83 Da |
Etymology
Another name for phlotoxin is μ-TRTX-Pspp-1: μ for NaV channel inhibition, then TRTX refers to theraphotoxin which refers to a group of toxins found in the Theraphosidae family.
Sources
Phlotoxin was first purified, characterized and sequenced from Phlogiellus sp. Phlogiellus is a genus of tarantulas. Its venom, which includes several neurotoxic peptides like phlotoxin, targets diverse ion channels and chemical receptors.
Chemistry
Structure
Phlotoxin-1 (PhlTx1), weighing around 4058.83 Da, is identified by a 34-amino acid sequence featuring three disulfide bridges and organized based on the Inhibitor Cystine Knot (ICK) architectural motif which is effective for its structural stabilization as three disulfide bonds are structured in a manner where two of them combine to create a circular arrangement, through which the third disulfide bond passes. It is classified to be a member of the NaV channel spider toxin (NaSpTx) family 1.
Symbol | Other names | Amino Acid Sequence |
---|---|---|
PhlTx1 | Mu-theraphotoxin-Pspp1 | -ACLGQWDSCDPKASKCCP—NYACEWKYP—WCRYKLF- |
The structure of phlotoxin comprises six cysteine residues forming an ICK architecture fold, with amidation occurring at the C-terminus. "Cys-Cys, Cys-Cys, Cys-Cys" disulfide bridge organization. The proximity of Cys 16 and 17 makes it challenging to synthesize even though phlotoxin is commercially available.
Homology
The sequence similarity of PhlTx1 with other peptides does not exceed 59%. The closest match regarding inhibition IC50 for PhlTx1 is found in the NaSpTx family to HnTx-III or HwTx-I. It is basically classified under the NaSpTx family, due to the presence of disulfide bridges. PhlTx1 is categorized within the NaSpTx-1 family primarily because of its disulfide bridges. Notably, the inclusion of three proline residues (Pro11, Pro18, and Pro27) introduces the potential for Cis–trans isomerism. This dynamic property can influence the precise formation of secondary structures and the correct alignment of disulfide bridges, thereby impacting the overall structural integrity of the toxin.
Target
In examining the effects of PhlTx1 on the sodium channel Nav1.7/β1, it appears to share similarities with TTX (tetrodotoxin). Both PhlTx1 and TTX exhibit a capacity to block the channel pore, resulting in a noticeable decrease in sodium currents. Moreover, the behavior of the channel, as reflected in gating parameters, remains largely unaffected by the presence of PhlTx1. This observation suggests a comparable behavior between PhlTx1 and TTX in modulating the function of Nav1.7/β1 channels. The IC50 for PhlTx1 to inhibit Nav1.7 is 39 +/- 2 nM.
The PhlTx1 affects all hNav (human voltage-gated Na channels) channels to a different degree except hNav1.8. There is a poor selectivity of PhlTx1 towards the hNav1.1 and 1.3. It also has shown a high affinity towards hNav1.7.
Mode of action
The amino acids which are critical for binding of the hNaV1.7 subtype are identified by their substitution with alanine. When tryptophan at position 24, lysine at position 25 and tyrosine at position 26 are replaced with alanine, there is a complete loss of affinity. This highlights the critical role of these amino acids in the binding process to Nav1.7. Other substitutions, like alanine at position 1, serine at position 8, lysine at position 12 or 15, result in a slight change (less than 2.8-fold) in variant affinity, whereas substituting aspartate at position 7 leads to an increase in variant affinity (IC50 = 47.0 ± 40.9).
Therapeutic use
Phlotoxin-1 (PhlTx1) has demonstrated selectivity in inhibiting the voltage-gated sodium channel NaV1.7. Its potential as an antinociceptive agent became apparent when a loss-of-function mutation in the NaV1.7 gene resulted in a congenital inability to perceive pain. Notably, these peptides do not independently exhibit antinociceptive effects; however, when co-administered with exogenous opioids, they bring about analgesic effect, allowing for a significant reduction in opioid dosage. The mechanism underlying the synergistic effect of opioid receptor agonists with selective NaV1.7 inhibitors remains unknown, but this discovery presents a novel approach to pain management. The primary method for evaluating this property involves the formalin test. However, the poor selectivity towards the hNav1.5 and 1.6 subtypes may be associated with in vivo cardiac and neuromuscular side effects, respectively, which could limit its potential use as an analgesic molecule.
References
- ^ Nicolas S, Zoukimian C, Bosmans F, Montnach J, Diochot S, Cuypers E, et al. (June 2019). "Chemical Synthesis, Proper Folding, Nav Channel Selectivity Profile and Analgesic Properties of the Spider Peptide Phlotoxin 1". Toxins. 11 (6): 367. doi:10.3390/toxins11060367. PMC 6628435. PMID 31234412.
- ^ Lopez SM, Aguilar JS, Fernandez JB, Lao AG, Estrella MR, Devanadera MK, et al. (2021). "Neuroactive venom compounds obtained from Phlogiellus bundokalbo as potential leads for neurodegenerative diseases: insights on their acetylcholinesterase and beta-secretase inhibitory activities in vitro". The Journal of Venomous Animals and Toxins Including Tropical Diseases. 27: e20210009. doi:10.1590/1678-9199-jvatitd-2021-0009. PMC 8237997. PMID 34249120.
- "Mu-theraphotoxin-Pspp1". UniProt. TXP1_PHLXX.
- ^ Gonçalves TC, Lesport P, Kuylle S, Stura E, Ciolek J, Mourier G, et al. (August 2019). "Evaluation of the Spider (Phlogiellus genus) Phlotoxin 1 and Synthetic Variants as Antinociceptive Drug Candidates". Toxins. 11 (9): 484. doi:10.3390/toxins11090484. PMC 6784069. PMID 31443554.
- ^ Deuis JR, Dekan Z, Wingerd JS, Smith JJ, Munasinghe NR, Bhola RF, et al. (January 2017). "Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a". Scientific Reports. 7 (1): 40883. Bibcode:2017NatSR...740883D. doi:10.1038/srep40883. PMC 5247677. PMID 28106092.
- Emery EC, Luiz AP, Wood JN (August 2016). "Nav1.7 and other voltage-gated sodium channels as drug targets for pain relief". Expert Opinion on Therapeutic Targets. 20 (8): 975–983. doi:10.1517/14728222.2016.1162295. PMC 4950419. PMID 26941184.
- Tjølsen A, Berge OG, Hunskaar S, Rosland JH, Hole K (October 1992). "The formalin test: an evaluation of the method". Pain. 51 (1): 5–17. doi:10.1016/0304-3959(92)90003-T. PMID 1454405. S2CID 32344519.
External links
- "Mu-theraphotoxin-Pspp1". AlphaFold structure prediction.
- "Mu-theraphotoxin-Pspp1". UniProt.