PURIFICATION AND CHARACTERIZATION OF THE ACTIVATED MINERALOCORTICOID RECEPTOR FROM RAT-KIDNEY

被引:13
|
作者
LAZAR, G
PAGANO, M
AGARWAL, MK
机构
[1] CTR UNIV CORDELIERS,UFR BROUSSAIS,DEPT BIOCHEM,F-75270 PARIS 06,FRANCE
[2] CTR UNIV CORDELIERS,UFR BROUSSAIS,DEPT PHYSIOL,F-75270 PARIS 06,FRANCE
[3] CTR UNIV CORDELIERS,UFR BROUSSAIS,HORMONE LAB,F-75270 PARIS 06,FRANCE
来源
INTERNATIONAL JOURNAL OF BIOCHEMISTRY | 1990年 / 22卷 / 06期
关键词
D O I
10.1016/0020-711X(90)90039-6
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
1. 1. The mineralcorticoid receptor (MR) from rat kidney was purified within 8hr by the following, successive steps: stabilization with synthetic, tritiated steroids (RU 26752 or R 5020), phosphocellulose passage, heat activation (25°C), and DNA-cellulose batch elution. 2. 2. The purified preparation was resolved as a single, 75 KDa band on SDS-PAGE electrophoresis although the exact degree of purity was difficult to assess by the charcoal assay due to denaturation. 3. 3. The natural hormone, aldosterone, was unsuitable for receptor purification and characterization. 4. 4. The MR purified with different ligands behaved identically during ion exchange and gel permeation analyses, suggesting post-translational modifications of the native receptor in whole cytosol that exhibits molecular heterogeneity. © 1990.
引用
收藏
页码:621 / 630
页数:10
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