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Human kidney amiloride-binding protein: cDNA structure and functional expression.

机译:人肾阿米洛利结合蛋白:cDNA结构和功能表达。

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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.
机译:Phenamil是阿米洛利的类似物,是上皮Na +通道的有效阻滞剂。它已被用于纯化猪肾阿米洛利结合蛋白。来源于部分序列的合成寡核苷酸已经用于筛选人肾脏cDNA文库并分离编码人阿米洛利结合蛋白的cDNA。从DNA序列分析推导了一级结构。该蛋白长713个残基,带有19个氨基酸的信号肽。 mRNA在293-S和NIH 3T3细胞中表达,产生一种糖蛋白(i)以与猪肾膜顶端Na +通道相关的阿米洛利受体相似的亲和力结合阿米洛利和阿米洛利类似物,以及(ii)用抗猪肾脏阿米洛利结合蛋白的单克隆抗体。

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