Intravenous Spike Protein Detoxification

COVID-19 victims are realizing that they have been genetically engineered with Moderna or Pfizer modifications of the Wuhan spike proteins. A collective panic has driven a quest for detoxification. This deadly protein is known to cause blood clotting and heart disease, as well as neurological injuries, over time.

Recent vulnerabilities in spike have been identified. These sites are known to be proteolytic cleavage locations where protein can be degraded by enzymes suitable for drug discovery. Nature has many such enzymes available, and worms are one of them.

A source of alkaline serine protease, abbreviated ASPNJ by the Japanese polychaete riverworm Neanthes japonica is known to be Izuka. “N” Neanthes japonica Liu et al. Liu et al.

“The Spike protein of wild-type SARS-CoV-2 was 1273 aa in length [2,25], containing 103 K and R residues. The prediction using the ExPASy peptide cutter and our experimental results showed that 101 R and K sites could be hydrolyzed by trypsin and ASPNJ, except for 462KP (P, proline, pro) and 811KP (Supplement Table S1). The 11 K sites (including 417K) and 11 R sites in RBD of S1, as well as the 682R, 683R, and 685R in the CendR motif of S1 and the 825K, 835K, 847R, and 854K in the fusion pepti