MOLECULAR-CLONING, STRUCTURAL CHARACTERIZATION AND FUNCTIONAL EXPRESSION OF THE HUMAN SUBSTANCE-P RECEPTOR

被引:169
|
作者
TAKEDA, Y
CHOU, KB
TAKEDA, J
SACHAIS, BS
KRAUSE, JE
机构
[1] Department of Anatomy, Neurobiology Washington University School of Medicine, St. Louis, MO 63110
关键词
D O I
10.1016/0006-291X(91)91704-G
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 ≫ neurokinin A > 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. © 1991.
引用
收藏
页码:1232 / 1240
页数:9
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