ABSTRACT
The protein composition of animal venoms is usually determined by peptide-centric proteomics approaches (bottom-up proteomics). However, this technique cannot, in most cases, distinguish among toxin proteoforms, herein called toxiforms, because of the protein inference problem. Top-down proteomics (TDP) analyzes intact proteins without digestion and provides high quality data to identify and characterize toxiforms. Denaturing top-down proteomics is the most disseminated subarea of TDP, which performs qualitative and quantitative analyzes of proteoforms up to ~30 kDa in high-throughput and automated fashion. On the other hand, native top-down proteomics provides access to information on large proteins (> 50 kDA) and protein interactions preserving non-covalent bonds and physiological complex stoichiometry. The use of native and denaturing top-down venomics introduced novel and useful techniques to toxinology, allowing an unprecedented characterization of venom proteins and protein complexes at the toxiform level. The collected data contribute to a deep understanding of venom natural history, open new possibilities to study the toxin evolution, and help in the development of better biotherapeutics.(AU)
Subject(s)
Peptides , Poisons/immunology , Toxicology , ProteomicsABSTRACT
Un grupo de cuatro ovinos sanos se inmunizó con veneno de Bothrops asper, para estudiar el desarrollo de la respuesta inmune, inducida por la aplicación de un esquema de hiperinmunización. Se tomaron muestras de sangre cada siete días en nueve oportunidades, con el suero obtenido se realizaron pruebas de neutralización en ratones. Se determinó la DE 50, la cual se expresó en µg de veneno neutralizado por ml de suero. Simultáneamente se observaron las condiciones generales de los ovinos durante el esquema de hiperinmunización, no presentándose alteraciones generales ni locales como consecuencia de la inoculación del veneno. En los resultados se observaron variaciones individuales en la magnitud de la elevación del título de anticuerpos y rasgos comunes en el comportamiento de las curvas desarrolladas. El título promedio óptimo (705,5 µg/ml), fue obtenido el día 21 posterior a la primera inoculación. Para ese momento, el ovino con título más alto fue de 840µg/ml y el más bajo, de 593 µg/ml. El promedio más bajo (308 µg/ml) fue observado el día 56. Se recomienda que los animales que serán utilizados en la producción comercial de antiveneno sean evaluados individualmente y seleccionados con base a una respuesta inmune satisfactoria.
A group of four (4) healthy male sheep were immunized with Bothrops asper venom, in order to study the development of the immune response induced by the application of a hiperimmunization protocol. Blood samples were taken from the sheep every seven days in nine different opportunities. With the resultant serum, neutralization tests were done in mice. ED50 was calculated and expressed in µg of neutralized venom per ml of serum, at the same time, general health conditions of sheep were observed during the hiperimmunization protocol. No general or local alterations of health were present as consequence of venom inoculations. Individual variations in the magnitude of the increase of antibody titles were observed in the obtained results. None the less common features in the antibody title curves were also recorded. The mean optimal average (705,5 µg/ml) was obtained on day 21 after the first challenge. At that time, the individual sheep with the highest value was 840 µg/ml and the lowest was 593 µg/ml; the lowest average of all samples (308 µg/ml ) was observed on day 56. It is recommend that animals to be used in the commercial venom antiserum production need to be individually screened and selected based on a satisfactory immune response.