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
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