Natural immunity is commonly affiliated with inherent antibodies in animals that have not been deliberately immunized. Most natural antibodies are of the IgM class. However, the natural immunity of snakes and certain warm- blooded animals to snake venoms involves non-immunoglobulin proteins. These proteins have a molecular weight range of 50,000 to 100,000 daltons and isoelectric points of 4-4.5. The neutralization capacities of the natural products are strong when compared to specific immunoglobulins and neutralize many hemorrhagic factors in different venoms. So far, the mechanism has been only partially elucidated, and further studies are required. The goals of the proposed research are to (a) compare the antigenic relationship of different hemorrhagins, (b) determine the range of the specificity and cross-reactivity of the antihemorrhagins isolated, (c) determine if the antihemorrhagic titer increase when the animal is challenged, (d) determine the exact mechanism (s) in the neutralization process, (e) determine the relationship of hemorrhagins to proteolytic inhibitors, (f) determine if a smaller nonantigenic segment of the antihemorrhagic molecule be used to neutralize hemorrhagic toxins, and (g) determine if the antihemorrhagic factors or a smaller segment can be used clinically. To achieve these goals, the PI will purify and characterize antihemorrhagic and hemorrhagic factors from warm-blooded animals and liquid chromatography (HPLC) will be used. To determine purity, electrophoresis, isoelectric focusing, and HPLC will be used. Electrophoresis, HPLC, and radioactive labeling will be used to study the mechanism of venom neutralization with the purified antihemorrhagic elucidation of the mechanism of neutralization with the purified antihemorrhagic and hemorrhage factors. Special attention will be devoted to elucidation of the mechanism of neutralization. Subsequent research will focus on determining the feasibility of inserting an opossum gene segment into E. Coli for the production of antihemorrhagic factors which could neutralize venom. Students, as in the past, will be involved in all phases of the research, including presentation at professional meetings and publishing in professional journals.

Project Start
Project End
Budget Start
Budget End
Support Year
19
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Texas A&M University-Kingsville
Department
Type
DUNS #
City
Kingsville
State
TX
Country
United States
Zip Code
78363
Zwink, Nadine; Jenetzky, Ekkehart (2018) Maternal drug use and the risk of anorectal malformations: systematic review and meta-analysis. Orphanet J Rare Dis 13:75
Garcia, Michelle R (2017) Leptin Contributes to the Development of the Corpus Luteum. Cell Dev Biol 6:
Wiles, Jessica R; Katchko, Robin A; Benavides, Elizabeth A et al. (2014) The effect of leptin on luteal angiogenic factors during the luteal phase of the estrous cycle in goats. Anim Reprod Sci 148:121-9
Saisawat, Pawaree; Kohl, Stefan; Hilger, Alina C et al. (2014) Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney Int 85:1310-7
Bartels, Enrika; Schulz, Anna C; Mora, Nicole W et al. (2012) VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol 21:191-5
Pathi, Satya S; Jose, Soumia; Govindaraju, Suman et al. (2012) zRICH, a protein induced during optic nerve regeneration in zebrafish, promotes neuritogenesis and interacts with tubulin. Brain Res 1474:29-39
Collier, C T; Williams, P N; Carroll, J A et al. (2011) Effect of maternal restraint stress during gestation on temporal lipopolysaccharide-induced neuroendocrine and immune responses of progeny. Domest Anim Endocrinol 40:40-50
Weber, Stefanie; Thiele, Holger; Mir, Sevgi et al. (2011) Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet 89:668-74
Sanchez, Elda E; Rodriguez-Acosta, Alexis; Palomar, Rene et al. (2009) Colombistatin: a disintegrin isolated from the venom of the South American snake (Bothrops colombiensis) that effectively inhibits platelet aggregation and SK-Mel-28 cell adhesion. Arch Toxicol 83:271-9
Salazar, Ana Maria; Guerrero, Belsy; Cantu, Bruno et al. (2009) Venom variation in hemostasis of the southern Pacific rattlesnake (Crotalus oreganus helleri): isolation of hellerase. Comp Biochem Physiol C Toxicol Pharmacol 149:307-16

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