作者: Valerie A. Ferro , Mohammad A. H. Khan , Elizabeth R. Earl , Michael J. A. Harvey , Angela Colston
DOI: 10.1034/J.1600-0897.2002.01120.X
关键词: Testosterone 、 Luteinizing hormone 、 Peptide 、 Peptide sequence 、 Follicle-stimulating hormone 、 Carbodiimide 、 Toxoid 、 Biology 、 Gonadotropin 、 Biochemistry
摘要: PROBLEM: We previously immunoneutralized gonadotrophin releasing hormone (GnRH), using an analogue of GnRH (des-1 GnRH-1), conjugated to tetanus toxoid via a carbodiimide reaction. The castration effect on the reproductive system was not consistent in all treated animals. Therefore, we examined possibility that conjugation carrier protein N- or C-terminal could have efficacy. METHOD OF STUDY: sequences were synthesized consisting additional cysteine at either terminal and specific carried out bifunctional linker agent. RESULTS: Conjugation monomer through N-terminal proved be highly effective means causing immunocastration terms decreased testosterone concentrations testicular size, whereas ineffective. This reflected ability antibodies bind native GnRH, but levels anti-GnRH antibodies. CONCLUSION: Immunoneutralization efficacy attributed importance preserving C-terminal.