Jørgensen P L, Petersen J, Rees W D
Biochim Biophys Acta. 1984 Aug 8;775(1):105-10. doi: 10.1016/0005-2736(84)90240-2.
A polypeptide of Mr 34 000 is photolabeled with [3H]bumethanide after binding of this drug to membranes from the outer renal medulla and irradiation at 345 nm, a wavelength where bumethanide has an absorption maximum. Our data show that the polypeptide of Mr 34 000 is a component of the Na+/K+/Cl--cotransport system. The [3H]bumethanide binding protein is not extracted by concentrations of the nonionic detergent C12E8 that solubilizes 67% of the protein of the membranes including (Na+ + K+)-ATPase. This step increases the capacity for binding of [3H]bumethanide to 681 pmol/mg protein. Extraction of the binding protein requires high ionic strength suggesting that the Na+/K+/Cl--cotransport protein is associated with cytoskeleton components. This association may be important for control of the entry of NaCl into the cytoplasm and for cellular regulation of the rate of active transport of NaCl across the tubule cells in the thick ascending limb of Henles loop.
一种分子量为34000的多肽在布美他尼与肾外髓质膜结合并在345nm波长(布美他尼在此波长有最大吸收峰)照射后,被[³H]布美他尼光标记。我们的数据表明,分子量为34000的多肽是Na⁺/K⁺/Cl⁻共转运系统的一个组成部分。[³H]布美他尼结合蛋白不能被非离子去污剂C12E8的浓度所提取,该去污剂可溶解包括(Na⁺ + K⁺)-ATP酶在内的67%的膜蛋白。这一步骤使[³H]布美他尼的结合能力增加到681pmol/mg蛋白。结合蛋白的提取需要高离子强度,这表明Na⁺/K⁺/Cl⁻共转运蛋白与细胞骨架成分有关。这种关联对于控制NaCl进入细胞质以及对Henle袢厚升支中NaCl跨肾小管细胞的主动转运速率的细胞调节可能很重要。