LaBelle E F, Lee S O
Biochemistry. 1982 May 25;21(11):2693-7. doi: 10.1021/bi00540a018.
An octyl glucoside extract has been formed from rabbit kidney medulla microsomes from which reconstituted proteoliposomes can be formed by lipid addition and dialysis to remove detergent. These proteoliposomes are capable of amiloride-inhibited 22Na+ transport. The amiloride-inhibited Na+ transport process is complete within 10 min and directly proportional to the vesicle protein concentration. Sodium accumulation by the proteoliposomes has been proven to represent transport by the demonstration that all Na+ taken up by the vesicles can be removed by the ionophore nigericin. The process has been shown to be specific for amiloride by the demonstration that the effect of amiloride on Na+ transport could not be reproduced by the similar compound sulfaguanidine nor by pyrazine, 2-pyrazinecarboxamide, 2-pyrazinecarboxylate, or 3-amino-2-pyrazinecarboxylate. The relationship between Na+ uptake into proteoliposomes and Na+ concentration was similar to the relationship between Na+ uptake and concentration observed with medulla microsomes. The concentration of amiloride required for half-maximal inhibition of Na+ uptake into either proteoliposomes or medulla microsomes was also the same. The evidence seems clear that the protein responsible for amiloride-inhibited Na+ transport into rabbit kidney medulla microsomes has been extracted from the membranes and incorporated into purified lipid vesicles.
已从兔肾髓质微粒体中提取出辛基葡糖苷提取物,通过添加脂质和透析去除去污剂,可由此形成重组蛋白脂质体。这些蛋白脂质体能够进行氨氯吡脒抑制的22Na+转运。氨氯吡脒抑制的Na+转运过程在10分钟内完成,且与囊泡蛋白浓度成正比。通过证明离子载体尼日利亚菌素可去除囊泡摄取的所有Na+,已证实蛋白脂质体的钠积累代表转运。通过证明氨氯吡脒对Na+转运的作用不能被类似化合物磺胺胍、吡嗪、2-吡嗪甲酰胺、2-吡嗪羧酸盐或3-氨基-2-吡嗪羧酸盐重现,已表明该过程对氨氯吡脒具有特异性。蛋白脂质体对Na+的摄取与Na+浓度之间的关系,类似于在髓质微粒体中观察到的Na+摄取与浓度之间的关系。抑制蛋白脂质体或髓质微粒体对Na+摄取达到半数最大抑制所需的氨氯吡脒浓度也相同。证据似乎很清楚,负责将氨氯吡脒抑制的Na+转运到兔肾髓质微粒体中的蛋白质已从膜中提取出来并整合到纯化的脂质囊泡中。