Structural highlights
Publication Abstract from PubMed
The need for molecules with high specificity against noxious insects leads the search towards spider venoms that have evolved highly selective toxins for insect preys. In this respect, spiders as a highly diversified group of almost exclusive insect predators appear to possess infinite potential for the discovery of novel insect-selective toxins. In 2003, a group of toxins was isolated from the spider Macrothele gigas and the amino acid sequence was reported. We obtained, by molecular biology techniques in a heterologous system, one of these toxins. Purification process was optimized by chromatographic methods to determine the three-dimensional structure by nuclear magnetic resonance in solution, and, finally, their biological activity was tested. rMagi3 resulted to be a specific insect toxin with no effect on mice.
Successful refolding and NMR structure of rMagi3: a disulfide-rich insecticidal spider toxin.,Titaux-Delgado G, Carrillo E, Mendoza A, Mayorga-Flores M, Escobedo-Gonzalez FC, Cano-Sanchez P, Lopez-Vera E, Corzo G, Del Rio-Portilla F Protein Sci. 2017 Dec 16. doi: 10.1002/pro.3363. PMID:29247580[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Titaux-Delgado G, Carrillo E, Mendoza A, Mayorga-Flores M, Escobedo-Gonzalez FC, Cano-Sanchez P, Lopez-Vera E, Corzo G, Del Rio-Portilla F. Successful refolding and NMR structure of rMagi3: a disulfide-rich insecticidal spider toxin. Protein Sci. 2017 Dec 16. doi: 10.1002/pro.3363. PMID:29247580 doi:http://dx.doi.org/10.1002/pro.3363