ISOLATION, PURIFICATION, AND CHARACTERIZATION OF CALCITONIN-GENE-RELATED PEPTIDE RECEPTOR

被引:27
作者
WIMALAWANSA, SJ [1 ]
GUNASEKERA, RD [1 ]
ZHANG, FG [1 ]
机构
[1] ROYAL POSTGRAD MED SCH,DEPT CHEM PATHOL,BIOCHEM ENDOCRINOL UNIT,LONDON W12 ONN,ENGLAND
关键词
AFFINITY CHROMATOGRAPHY; SDS-PAGE; MOLECULAR WEIGHT; MEMBRANE RECEPTORS; CEREBELLUM;
D O I
10.1016/0196-9781(93)90099-3
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
Intact calcitonin gene-related peptide (CGRP) receptors were solubilized from porcine neural membranes using sodium cholate:potassium buffer. The solubilized receptors were purified sequentially by hydrophobic interaction and ion-exchange chromatography.followed by specific affinity chromatography. Using these procedures, we have isolated 2 nmol of highly purified active CGRP receptor to a homogeneity (5 X 10(8)-fold purification). The isolated receptors retained their specificity and the capacity to bind to I-125-CGRP, and showed no cross-reactivity with a number of other peptides, except with amylin having 46% amino acid sequence homology to h-CGRP. The solubilized receptors were adsorbed by WGA-agarose and concanavalin-A, suggesting a glycoprotein nature. SDS-PAGE, size-exclusion HPLC, and autoradiography confirmed that CGRP receptor is a monomeric membrane protein with M(r) 66 kDa.
引用
收藏
页码:691 / 699
页数:9
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