Design of angiotensin II derivatives suitable for indirect affinity techniques: potential applications to receptor studies.

The design of angiotensin II (A II)-derived probes suitable for indirect affinity techniques is presented. Biotin or dinitrophenyl moieties have been added at the N-terminus of A II, through aminohexanoic acid as spacer arm, to generate (6-biotinylamido)-hexanoyl-AII (Bio-Ahx-AII) and dinitrophenyl- aminohexanoyl-AII (Dnp-Ahx-AII). Monoiodinated and highly labeled radioiodinated forms of these probes have been prepared. The two bifunctional ligands displayed high affinities for rat liver A II receptors (Kd values in the nanomolar range) and their secondary acceptors: streptavidin and monoclonal anti-Dnp antibodies respectively. Bio-Ahx-AII and Dnp-Ahx-AII behaved as agonists on several AII-sensitive systems. Based on these structural assessments, the parent photoactivable azido probe: Bio-Ahx-(Ala1,Phe(4N3)8)A II. A II was synthesized and proved to possess similar biological properties than the non-azido compound. The hepatic A II receptor could be covalently labeled by the radioiodinated probe, with a particularly high yield (15-20%); SDS-polyacrylamide gel electrophoresis of solubilized complexes revealed specific labeling of a 65 Kdaltons binding unit, in agreement with previous data obtained with other azido AII-derived compounds. The potential applications of these probes are: i) receptor purification by combination of its photoaffinity labeling and adsorption of biotin-tagged solubilized hormone-receptor complexes on avidin gels. ii) cell labeling and sorting. iii) histochemical receptor visualization.

[1]  G. Guillon,et al.  High yield photoaffinity labeling of angiotensin II receptors. , 1986, Molecular pharmacology.

[2]  H. Nakayama,et al.  Affinity purification of the opioid receptor in NG 108‐15 cells using an avidin‐biotin system with a novel elution method , 1986, FEBS letters.

[3]  A. Niendorf,et al.  Cytochemical studies of corticotropin-releasing factor (CRF) receptors in anterior lobe corticotropes: binding, glucocorticoid regulation, and endocytosis of [biotinyl-Ser1]CRF. , 1986, Endocrinology.

[4]  E. Hazum,et al.  Solubilization and purification of rat pituitary gonadotropin-releasing hormone receptor. , 1986, The Journal of biological chemistry.

[5]  G. Guillon,et al.  Vasopressin induces breakdown of membrane phosphoinositides in adrenal glomerulosa and fasciculata cells. , 1986, Endocrinology.

[6]  A. Bothner‐By,et al.  Radioactive probes for adrenocorticotropic hormone receptors. , 1986, Biochemistry.

[7]  X. Breakefield,et al.  Receptor Binding Activities of Biotinylated Derivatives of β‐Nerve Growth Factor , 1986 .

[8]  E. Baulieu,et al.  The use of the biotinyl estradiol-avidin system for the purification of "nontransformed" estrogen receptor by biohormonal affinity chromatography. , 1985, The Journal of biological chemistry.

[9]  K. Hofmann,et al.  [37] Synthesis of biotinyl derivatives of peptide hormones and other biological materials , 1985 .

[10]  S. Lavielle,et al.  Binding affinities to rat brain synaptosomes--synthesis of biotinylated analogues of Substance P. , 2009, International journal of peptide and protein research.

[11]  K. Hofmann,et al.  Avidin-biotin affinity chromatography: application to the isolation of human placental insulin receptor. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[12]  R. Ardaillou,et al.  Solubization of angiotensin II receptors in rat glomeruli , 1984, FEBS letters.

[13]  I. Sen,et al.  Isolation of an angiotensin II-binding protein from liver. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. Wilchek,et al.  The avidin-biotin complex in immunology. , 1984, Immunology today.

[15]  G. Guillon,et al.  Angiotensin-induced changes in the apparent size of rat liver angiotensin receptors. , 1984, Journal of receptor research.

[16]  I. Sen,et al.  Solubilization and characterization of an angiotensin II binding protein from liver. , 1983, European journal of biochemistry.

[17]  M. Aubert,et al.  Binding sites for lactogenic and somatogenic hormones from rabbit mammary gland and liver. , 1983, The Journal of biological chemistry.

[18]  M. Vallotton,et al.  Solubilization of adrenal angiotensin II receptors with a zwitterionic detergent. , 1983, Journal of receptor research.

[19]  S. Jard,et al.  The liver angiotensin receptor involved in the activation of glycogen phosphorylase. , 1982, The Biochemical journal.

[20]  G. Orr,et al.  The purification of avidin and its derivatives on 2-iminobiotin-6-aminohexyl-Sepharose 4B. , 1981, Analytical biochemistry.

[21]  E. Escher,et al.  Photoaffinity labeling of the angiotensin II receptor. 1. Synthesis and biological activities of the labeling peptides. , 1978, Journal of medicinal chemistry.

[22]  P. Fraker,et al.  Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphrenylglycoluril. , 1978, Biochemical and biophysical research communications.

[23]  C. Selve,et al.  Reactifs de couplage peptidique I (1) - l'hexafluorophosphate de benzotriazolyl N-oxytrisdimethylamino phosphonium (B.O.P.) , 1975 .

[24]  D. Regoli,et al.  Role of the N-terminal amino acid for the biological activities of angiotensin and inhibitory analogues. , 1974, Canadian journal of physiology and pharmacology.

[25]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[26]  D. Neville Isolation of an organ specific protein antigen from cell-surface membrane of rat liver. , 1968, Biochimica et biophysica acta.

[27]  S. Shaltiel Thiolysis of some dinitrophenyl derivatives of amino acids. , 1967, Biochemical and biophysical research communications.

[28]  A. Smoczkiewiczowa,et al.  Separation and Determination of Millimicrogram Amounts of Cobalt and Microgram Amounts of Copper in Biological Material , 1958, Nature.

[29]  A. Mcfarlane,et al.  Efficient Trace-labelling of Proteins with Iodine , 1958, Nature.