Low W, Kasir J, Rahamimoff H
Department of Biochemistry, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
FEBS Lett. 1993 Jan 18;316(1):63-7. doi: 10.1016/0014-5793(93)81737-k.
A functional rat heart Na(+)-Ca2+ exchanger gene has been obtained by splicing and ligating two partially overlapping clones isolated from a rat heart lambda ZAP cDNA library. The deduced primary structure of the protein encoded by the open reading frame corresponds to 971 amino acids, that can be organized into 12 transmembrane helices. The cloned gene was functionally expressed in HeLa cells. Maximal expression was detected 18 h after transfection, after which transport activity rapidly declined. The electrogenic properties of the cloned transporter were demonstrated following reconstitution of the expressed exchanger protein into a tightly sealed phospholipid membrane.
通过拼接和连接从大鼠心脏λZAP cDNA文库中分离出的两个部分重叠的克隆,获得了一个具有功能的大鼠心脏钠钙交换器基因。开放阅读框编码的蛋白质的推导一级结构对应于971个氨基酸,可组织成12个跨膜螺旋。克隆的基因在HeLa细胞中进行了功能表达。转染后18小时检测到最大表达,此后转运活性迅速下降。将表达的交换蛋白重组到紧密密封的磷脂膜中后,证明了克隆转运体的生电特性。