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Tachykinin NK-1 receptor probed with constrained analogues of substance P
Authors:Sandrine Sagan,Hubert Josien,Philippe Karoyan,Alié   Brunissen,Gé  rard Chassaing,Solange Lavielle
Affiliation:

Laboratoire de Chimie Organique Biologique, CNRS URA 493, Université P. et M. Curie, 4, place Jussieu, 75005, Paris, France

Abstract:The action of rotameric probes introduced either in position 7 or 8 in the sequence of substance P (SP) was investigated, i.e. -tetrahydroisoquinoleic acid (Tic), -fluorenylglycine (Flg), -diphenylalanine (Dip), the diastereoisomers of -1-indanylglycine (Ing) and -benz[ƒ]indanylglycine (Bfi), the Z- and E-isomers of dehydrophenylalanine and dehydronaphthylalanine (ΔZPhe, ΔEPhe, ΔZNal, ΔENal) and (Dmp). The aim of this study was the topographical characterization of the binding subsites of human NK-1 receptor expressed in CHO cells, especially the S7 and S8 subsites, corresponding to residues Phe7 and Phe8 of substance P. According to the binding potencies of these substituted-SP analogues, the S7 binding subsite is smaller than the S8 subsite: the S7 subsite accepts only one aromatic nucleus, while the S8 can accommodate three coplanar nuclei altogether. These findings are compatible with the idea that the S8 binding subsite may reside in the extracellular loops of the hNK-1 receptor. NK-1 agonists bind to human NK-1 receptor and activate the production of both inositol phosphates and cyclic AMP. As already quoted for septide, [pGlu6, Pro9]SP(6–11), discrepancies are observed between affinity (Ki) and activity (EC50) values for IPs production. While a weak correlation between Ki and EC50 values for IPs production could be found (r = 0.70), an excellent correlation could be demonstrated between their affinities (Ki) and their potencies (EC50) for cAMP production (r = 0.97). The high potency (EC50) observed for ‘septide-like’ molecules on PI hydrolysis, compared to their affinity is not an artefact related to the high level of NK-1 receptors expressed on CHO cells since a good correlation was found between EC50 values obtained for PI hydrolysis and those measured for spasmogenic activity in guinea pig ileum bioassay (r = 0.94).

According to the binding potencies of constrained analogues of phenylalanine, the S7 binding subsite of human NK-1 receptor is small, whereas the S8, which can accommodate three coplanar nuclei, might probably reside in the extracellular loop. The discrepancies observed between affinity (Ki) and activity (EC50) values for IPs production are not an artefact of CHO cells since a good correlation was found between EC50 for PI hydrolysis and those measured in guinea pig ileum bioassay.

Keywords:Abbreviations: the abbreviations for the amino acids are in accordance with the recommendations of the IUPAC-IUB Joint Commission on Biochemical nomenclature (Eur. J. Chem.1984, 138, 9). The symbols represent the   font-variant: small-caps"  >l-isomer except when indicated otherwise. For the three code-letters nomenclature of the non-natural amino acids see Fig. 1, and footnote of Fig. 1. The other abbreviations used are as follows: CHO cells, Chinese hamster ovary cells   PI, phosphatidylinositol   cAMP, cyclic adenosine 5′-phosphate   GPI, guinea-pig ileum   SDS, sodium dodecyl sulfate   THF, tetrahydrofuran   LDA, lithium diisopropyl amide   HMPA, hexamethylphosphorous triamide   TFA, trifluoroacetic acid   TLC, thin layer chromatography   HPLC, high pressure liquid chromatography   NMR, nuclear magnetic resonance   DMF, dimethylformamide   DMSO, dimethylsulfoxide
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