Oxotoxin Explained

Oxotoxins, or oxytoxins, are a group of neurotoxins present in the venom of lynx spiders belonging to the genus Oxyopes, hence the name oxytoxin. They are disulfide-rich peptides. Only two types are so far reported from two different species, the larger oxytoxin 1 (OxyTx1) from Oxyopes kitabensis, and the smaller oxytoxin 2 (OxyTx2) from Oxyopes lineatus. OxyTx1, the first known oxytoxin, was discovered in 2002. It was found to enhance the lethal efficacy of the spider venom by acting together with oxyopinins.[1] It is composed of 69 amino acid residue, which are cross-linked by five disulfide bridges. It is a large peptide having a molecular mass of 8059.2 Da; but shows the size of 9,109.4 Da due to the presence of disulfide bridges. It is a potent insecticide, but non-toxic to mice up to 1 μg/20-g mouse. It acts synergistically with oxyopinins of the same venom to increase the insecticidal effect.

Both OxyTx1 and OxyTx2 were isolated in 2008 from O. lineatus.[2] Both of these toxins were found to block voltage-sensitive calcium ion channels. OxyTx2 is made up of 55 amino acid residues and has a molecular mass 6175.2 Da. It is less effective in causing paralysis in Spodoptera litura larvae than Oxytx1.

Types

Oxotoxins are classified as follows:

NameRecommended nameSize in DaAmino acid residueToxicity (LD50) on S. litura
Oxytoxin 1 Omega-oxotoxin-Ol1a 8058.2 69 5.0 nmol/g
Oxytoxin 2 Omega-oxotoxin-Ol1b 6,186 55 weak activity

External links

Notes and References

  1. Corzo G, Villegas E, Gómez-Lagunas F, Possani LD, Belokoneva OS, Nakajima T . 2002 . Oxyopinins, large amphipathic peptides isolated from the venom of the wolf spider Oxyopes kitabensis with cytolytic properties and positive insecticidal cooperativity with spider neurotoxins . J Biol Chem . 277 . 26 . 23627–23637 . 11976325. 10.1074/jbc.M200511200. free .
  2. Villegas E, Adachi-Akahane S, Bosmans F, Tytgat J, Nakajima T, Corzo G . 2008 . Biochemical characterization of cysteine-rich peptides from Oxyopes sp. venom that block calcium ion channels. Toxicon . 52 . 2 . 228–236 . 18606178. 10.1016/j.toxicon.2008.05.019.