Radiolabelling by tritium and [125I]iodine of an angiotensin II related Peptide
| Autor: | J. P. Beaucourt, C. Ramombordes, C. Perret, M Budisavljevic, P. Pham, P. Verroust, P. Ronco |
|---|---|
| Rok vydání: | 1991 |
| Předmět: |
chemistry.chemical_classification
Stereochemistry Organic Chemistry Peptide Plasma protein binding Biochemistry Angiotensin II Analytical Chemistry chemistry.chemical_compound chemistry Labelling Drug Discovery Chloramine-T Radiology Nuclear Medicine and imaging Tritium Amine gas treating Receptor Spectroscopy |
| Zdroj: | Journal of Labelled Compounds and Radiopharmaceuticals. 29:575-581 |
| ISSN: | 0362-4803 |
| DOI: | 10.1002/jlcr.2580290509 |
| Popis: | We describe the 3H- and 125I- labelling of Glu-Gly-Val-Tyr-Val-His-Pro-Val, (hIIA), an octapeptide encoded by an RNA strand complementary to the human angiotensin II (AII) mRNA. The labelling of this peptide with 125I was performed by two ways : 1/ Mono-iodination of the Tyr residue, using Na125I in the presence of Chloramine T; 2/ Coupling of the [125I]Bolton-Hunter reagent to the terminal amine group of the octapeptide. The synthesis of the tritiated (3,5-3H2-Tyr4)octapeptide was achieved by a two step synthesis : di-iodination of the peptide followed by its catalytic dehalogenation in the presence of tritium gas. The compounds obtained inhibited the binding of AII to its receptors or antibodies but showed no direct binding to these proteins, suggesting no competition between AII and hIIA for these protein binding sites. Nous avons effectue le marquage radioactif par le tritium et l'iode 125 d'un octapeptide code par l'ARN complementaire de l'ARN messager de l'angiotensine II humaine. Deux types de marquage a l'iode 125 ont ete utilises : 1/ introduction de l'iode en α de l'hydroxyle phenolique du residu Tyr par Na125I en presence de Chloramine T; 2/ couplage du reactif [125I]Bolton Hunter au groupement amine terminal du peptide. La synthese du derive trite au niveau du residu tyrosyle est realisee en deux etapes : formation d'un derive diiode (3,5-I2-Tyr4)octapeptide, puis deshalogenation catalytique en presence de tritium gazeux. Les produits obtenus inhibent les liaisons AII-recepteur ou -anticorps mais ne se lient pas specifiquement a ces proteines, suggerant l'absence de competition entre AII et hIIA pour ces sites proteiques. |
| Databáze: | OpenAIRE |
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