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

被引:171
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
相关论文
共 25 条
[1]   PHOTOAFFINITY-LABELING THE SUBSTANCE-P RECEPTOR USING A DERIVATIVE OF SUBSTANCE-P CONTAINING P-BENZOYLPHENYLALANINE [J].
BOYD, ND ;
WHITE, CF ;
CERPA, R ;
KAISER, ET ;
LEEMAN, SE .
BIOCHEMISTRY, 1991, 30 (02) :336-342
[2]   A SIMPLE, SENSITIVE, AND SPECIFIC RADIORECEPTOR ASSAY FOR INOSITOL 1,4,5-TRISPHOSPHATE IN BIOLOGICAL TISSUES [J].
BREDT, DS ;
MOUREY, RJ ;
SNYDER, SH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 159 (03) :976-982
[3]  
CARTER MS, 1990, J NEUROSCI, V10, P2203
[4]  
CASCIERI MA, 1983, J BIOL CHEM, V258, P5158
[5]   MASS MEASUREMENTS OF INOSITOL(1,4,5)TRISPHOSPHATE IN RAT CEREBRAL-CORTEX SLICES USING A RADIORECEPTOR ASSAY - EFFECTS OF NEUROTRANSMITTERS AND DEPOLARIZATION [J].
CHALLISS, RAJ ;
BATTY, IH ;
NAHORSKI, SR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (02) :684-691
[6]   AMINO-ACID SEQUENCE OF SUBSTANCE P [J].
CHANG, MM ;
LEEMAN, SE ;
NIALL, HD .
NATURE-NEW BIOLOGY, 1971, 232 (29) :86-+
[7]   DIVERSITY IN MAMMALIAN TACHYKININ PEPTIDERGIC NEURONS - MULTIPLE PEPTIDES, RECEPTORS, AND REGULATORY MECHANISMS [J].
HELKE, CJ ;
KRAUSE, JE ;
MANTYH, PW ;
COUTURE, R ;
BANNON, MJ .
FASEB JOURNAL, 1990, 4 (06) :1606-1615
[8]  
HERSHEY AD, 1991, J BIOL CHEM, V266, P4366
[9]   MOLECULAR CHARACTERIZATION OF A FUNCTIONAL CDNA-ENCODING THE RAT SUBSTANCE-P RECEPTOR [J].
HERSHEY, AD ;
KRAUSE, JE .
SCIENCE, 1990, 247 (4945) :958-962
[10]  
HERSHEY AD, 1991, THESIS WASHINGTON U