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- W64902986 abstract "The authors recently showed that human platelets bear specific vasopressin (AVP) V1-vascular receptors. They now present the identification of AVP intra-platelet messenger and solubilization of AVP receptors. AVP binding to its platelet receptors is modulated by divalent cations but not TP or Gpp(NH)p, (10 /sup 3/M). AVP-induced reduction of adenylate cyclase activity is blocked by a phospholipase C inhibitor. In the presence of calcium (1 mM), AVP stimulates the phosphorylation of two endogenous proteins (M.W. = 40,000 and 20,000 daltons) which are substrates for protein kinase C and calcium calmodulin-dependent kinase, respectively. Phosphorylation is also stimulated by a V1-vascular agonist but not V2-renal agonists and is more potently blocked by a V1-vascular antagonist than by a V2-renal antagonist. AVP platelet membrane receptor is solubilized with 3-((3-cholamidopropyl)-dimethylammonio)-1-propane sulfonate. Separation of free (/sub 3/H)AVP from solubilized receptor-hormone complexes is done by filtration through polyethylenimine-treated filters. The solubilized receptor retains its binding characteristics (Kd = 11.03 +/- 1.86 nM, Bmax 288 +/- 66 fmol/mg protein, n = 6). In human platelets, AVP intra-cellular messengers are diacylglycerol and calcium, not adenylate cyclase. Solubilization of AVP human receptor opens the way to its purification." @default.
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- W64902986 date "1986-03-01" @default.
- W64902986 modified "2023-09-23" @default.
- W64902986 title "Characterization and solubilization of the human platelet vasopressin receptor" @default.
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