HUMAN KIDNEY AMILORIDE-BINDING PROTEIN - CDNA STRUCTURE AND FUNCTIONAL EXPRESSION

被引:75
作者
BARBRY, P
CHAMPE, M
CHASSANDE, O
MUNEMITSU, S
CHAMPIGNY, G
LINGUEGLIA, E
MAES, P
FRELIN, C
TARTAR, A
ULLRICH, A
LAZDUNSKI, M
机构
[1] GENENTECH INC,S SAN FRANCISCO,CA 94080
[2] INST PASTEUR,CNRS,UA 1309,SERV CHIM MOLEC,F-59019 LILLE,FRANCE
关键词
Epithelium; Na[!sup]+[!/sup] transport; Primary sequence;
D O I
10.1073/pnas.87.19.7347
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Phenamil, an analog of amiloride, is a potent blocker of the epithelial Na+ channel. It has been used to purify the porcine kidney amiloride-binding protein. Synthetic oligonucleotides derived from partial sequences have been used to screen a human kidney cDNA library and to isolate the cDNA encoding the human amiloride-binding protein. The primary structure was deduced from the DNA sequence analysis. The protein is 713 residues long, with a 19-amino acid signal peptide. The mRNA was expressed in 293-S and NIH 3T3 cells, yielding a glycoprotein (i) that binds amiloride and amiloride analogs with affinities similar to the amiloride receptor associated with the apical Na+ channel in pig kidney membranes and (ii) that is immunoprecipitated with monoclonal antibodies raised against pig kidney amiloride-binding protein.
引用
收藏
页码:7347 / 7351
页数:5
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