Production of Polyclonal Antibody to the Bovine Adrenal Atrial Natriuretic Factor-R1 Receptor
| Autor: | N. McNicoll, Jean Gagnon, C Lord, L. Larose, Huy Ong, A. De Lean, J J Rondeau, S. Meloche |
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| Rok vydání: | 1992 |
| Předmět: |
Molecular Sequence Data
Radioimmunoassay Epitope Iodine Radioisotopes Rats Sprague-Dawley Epitopes chemistry.chemical_compound Atrial natriuretic peptide Antibody Specificity Adrenal Glands medicine Animals Trypsin Amino Acid Sequence Receptor Peptide sequence Pharmacology Sequence Homology Amino Acid biology Rats chemistry Biochemistry Guanylate Cyclase Polyclonal antibodies Antibody Formation biology.protein Cattle Cyanogen bromide Antibody Protein Kinases Receptors Atrial Natriuretic Factor Atrial Natriuretic Factor medicine.drug |
| Zdroj: | Journal of Receptor Research. 12:485-505 |
| ISSN: | 0197-5110 |
| DOI: | 10.3109/10799899209074808 |
| Popis: | A polyclonal antibody monospecific for an intracellular epitope of the atrial natriuretic factor (ANF)-R1 receptor was produced. The receptor protein (200 pmoles) was purified to homogeneity from bovine adrenal zona glomerulosa (BAZG), reduced, alkylated and digested with trypsin. The tryptic fragments were purified by reverse-phase h.p.l.c. on a C18 column. Based on the sequence of one of these fragments, a peptide was chemically synthesized, coupled to thyroglobulin and injected into rabbits. The antibody obtained was shown to be specific for the R1-type as no receptor was detected in bovine red blood cells (RBC) (which are devoid of ANF receptors) and in NIH-3T3 cell membranes (where only the R2-type is expressed). Several other tissues were screened and comparison of the immunoreactive receptor density estimates with those obtained by ANF binding yielded a correlation coefficient (r2) of 0.965. The minimal detectable dose was typically 3 fmoles/tube and the ED50 of the RIA was 30 fmoles/tube. Cyanogen bromide digestion of the receptor was essential for antigenic detection, indicating that the epitope is probably hindered due to the tertiary structure of the native protein. Moreover, location of the epitope in the kinase homology domain of the receptor, combined with partial tryptic digestion, suggests that the proteolysis-sensitive region of the receptor is located between the transmembrane-spanning domain and the amino acid 586. This method of production of antibodies should be useful to precisely map the amino acids involved in various functions of the receptor. |
| Databáze: | OpenAIRE |
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