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Biochem Biophys Res Commun ; 179(3): 1232-40, 1991 Sep 30.
Article in English | MEDLINE | ID: mdl-1718267

ABSTRACT

A cDNA encoding the human substance P receptor (SPR) was isolated and the primary structure of the protein was deduced by nucleotide sequence analysis. This SPR consists of 407 residues and is a member of the G-protein coupled receptor superfamily. Comparison of rat and human SPR sequences demonstrated a 94.5% identity. The receptor was expressed in a COS-7 cell line and displayed a Kd for Tyr-1-SP binding of 0.24 nM. Ligand displacement by naturally occurring tachykinin peptides was SP much greater than neurokinin A greater than neurokinin B. SP stimulation of transfected cells resulted in a rapid and transient inositol 1,4,5-trisphosphate response. RNA blot hybridization and solution hybridization demonstrated that SPR mRNA was about 4.5 Kb in size, and was expressed in IM-9 lymphoblast and U373-MG astrocytoma cells, as well as in spinal cord and lung but not in liver.


Subject(s)
Receptors, Neurotransmitter/genetics , Amino Acid Sequence , Animals , Base Sequence , Binding, Competitive , Cell Line , Cloning, Molecular/methods , DNA/genetics , DNA/isolation & purification , Exons , Humans , Inositol 1,4,5-Trisphosphate/metabolism , Kinetics , Molecular Sequence Data , Oligodeoxyribonucleotides , Polymerase Chain Reaction/methods , RNA, Messenger/genetics , Rats , Receptors, Neurokinin-1 , Receptors, Neurotransmitter/metabolism , Recombinant Proteins/metabolism , Sequence Homology, Nucleic Acid , Substance P/metabolism , Transfection
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