STRUCTURAL CHARACTERIZATION OF CANINE PYY

被引:38
作者
EYSSELEIN, VE
EBERLEIN, GA
GRANDT, D
SCHAEFFER, M
ZEHRES, B
BEHN, U
SCHAEFER, D
GOEBELL, H
DAVIS, M
LEE, TD
SHIVELY, JE
MEYER, HE
REEVE, JR
机构
[1] CALIF BIOTECHNOL INC,MT VIEW,CA 94043
[2] UNIV ESSEN GESAMTHSCH,DEPT GASTROENTEROL & SURG,W-4300 ESSEN 1,GERMANY
[3] CITY HOPE NATL MED CTR,BECKMAN RES INT,DIV IMMUNOL,DUARTE,CA 91010
[4] RUHR UNIV BOCHUM,INST PHYSIOL CHEM 1,W-4630 BOCHUM,GERMANY
[5] UNIV CALIF LOS ANGELES,VET ADM WADSWORTH MED CTR,CTR ULCER RES & EDUC,DEPT MED,LOS ANGELES,CA 90073
关键词
Fast protein liquid chromatography; Gastric acid secretion; gastrointestinal hormones; High performance liquid chromatography; Microsequence analysis; Molecular heterogeneity; Motility; Neuropeptide Y (NPY); Pancreatic secretion; Peptide YY (PYY); Radioimmunoassay;
D O I
10.1016/0196-9781(90)90118-O
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
PYY was purified from canine colonic mucosa by sequential steps of reverse phase HPLC and ion-exchange FPLC. Microsequence, amino acid and mass spectral analyses of the purified peptide and its tryptic fragments were consistent with the structure: YPAKPEAPGEDASPEELSRYYASLRHYLNLVTRQRY-amide. Canine PYY(1-36) has the identical sequence as porcine and rat PYY but differs from human PYY at position 3, with Ala instead of Ile, and position 18, with Ser instead of Asn. A smaller form, PYY(3-36), was also purified and characterized. It may differ in its biological activity from the intact peptide and could act as a partial antagonist or agonist of PYY(1-36). © 1990.
引用
收藏
页码:111 / 116
页数:6
相关论文
共 30 条
[11]  
HAWKE D, 1982, ANAL BIOCHEM, V120, P302, DOI 10.1016/0003-2697(82)90351-7
[12]   CHARACTERIZATION OF PEPTIDE-YY RECEPTORS IN THE BRAIN [J].
INUI, A ;
OKITA, M ;
INOUE, T ;
SAKATANI, N ;
OYA, M ;
MORIOKA, H ;
SHII, K ;
YOKONO, K ;
MIZUNO, N ;
BABA, S .
ENDOCRINOLOGY, 1989, 124 (01) :402-409
[13]   SUCCESSIVE CLEAVAGE OF N-TERMINAL ARG1-PRO2 AND LYS3-PRO4 FROM SUBSTANCE-P BUT NO RELEASE OF ARG1-PRO2 FROM BRADYKININ, BY X-PRO DIPEPTIDYL-AMINOPEPTIDASE [J].
KATO, T ;
NAGATSU, T ;
FUKASAWA, K ;
HARADA, M ;
NAGATSU, I ;
SAKAKIBARA, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 525 (02) :417-422
[14]   PEPTIDE-YY INHIBITS NUTRIENT-STIMULATED, HORMONAL-STIMULATED, AND VAGALLY-STIMULATED PANCREATIC EXOCRINE SECRETION [J].
LLUIS, F ;
GOMEZ, G ;
FUJIMURA, M ;
GREELEY, GH ;
THOMPSON, JC .
PANCREAS, 1987, 2 (04) :454-462
[15]   VASCULAR EFFECTS OF THE PEPTIDES PYY AND PHI - COMPARISON WITH APP AND VIP [J].
LUNDBERG, JM ;
TATEMOTO, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1982, 83 (1-2) :143-146
[16]   PANCREATIC-POLYPEPTIDE FAMILY (APP, BPP, NPY AND PYY) IN RELATION TO SYMPATHETIC VASOCONSTRICTION RESISTANT TO ALPHA-ADRENOCEPTOR BLOCKADE [J].
LUNDBERG, JM ;
TATEMOTO, K .
ACTA PHYSIOLOGICA SCANDINAVICA, 1982, 116 (04) :393-402
[17]   PEPTIDE-YY RELEASE BY FATTY-ACIDS IS SUFFICIENT TO INHIBIT GASTRIC-EMPTYING IN DOGS [J].
PAPPAS, TN ;
DEBAS, HT ;
CHANG, AM ;
TAYLOR, IL .
GASTROENTEROLOGY, 1986, 91 (06) :1386-1389
[18]   ENTEROGASTRONE-LIKE EFFECT OF PEPTIDE YY IS VAGALLY MEDIATED IN THE DOG [J].
PAPPAS, TN ;
DEBAS, HT ;
TAYLOR, IL .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (01) :49-53
[19]   PEPTIDE-YY - METABOLISM AND EFFECT ON PANCREATIC-SECRETION IN DOGS [J].
PAPPAS, TN ;
DEBAS, HT ;
TAYLOR, IL .
GASTROENTEROLOGY, 1985, 89 (06) :1387-1392
[20]  
REEVE JR, 1983, J BIOL CHEM, V258, P5582