Longoni S, Carafoli E
Biochem Biophys Res Commun. 1987 Jun 30;145(3):1059-63. doi: 10.1016/0006-291x(87)91544-0.
The Na+/Ca2+ exchanger of calf heart sarcolemma has been identified in solubilized membrane preparations with the help of specific antibodies as a molecule of approximate Mr of 30 KDa. The conclusion supports the previous proposal by Soldati et al. (J. Biol. Chem. 260, 13321-13327, 1985) that the exchanger is a molecule of Mr about 33 KDa. Antibodies (IgG) were raised in rabbits by injecting proteins electroeluted from different regions of preparative SDS gels of solubilized heart sarcolemma. After purification the IgG against the proteins of the 30 KDa region recognized the 33 KDa component but also proteins of Mr about 70 and 140 KDa. Conversely, antibodies against the 140 KDa protein(s) also recognized the 70 and the 33 KDa proteins. However, if the solubilized sarcolemma extract was treated with DTT prior to the transfer to nitrocellulose the 140 KDa protein was not seen. Both the antibodies against the 30 KDa and those against the 140 KDa proteins inhibited the Na+/Ca2+ exchange activity of sarcolemma vesicles. It is proposed that the basic unit of the Na+/Ca2+ exchanger of heart sarcolemma is a monomer of Mr about 33 KDa, the functionally active exchanger being a tetramer in which the four 33 KDa subunits are held together by disulfide bonds. In the monomer-tetramer transition an intermediate dimeric state of Mr 70 KDa is also formed.
利用特异性抗体,在溶解的膜制剂中已鉴定出小牛心脏肌膜的钠/钙交换体是一种分子量约为30 kDa的分子。这一结论支持了索尔达蒂等人(《生物化学杂志》260, 13321 - 13327, 1985)之前的提议,即该交换体是一种分子量约为33 kDa的分子。通过注射从溶解的心脏肌膜制备的SDS凝胶不同区域电洗脱的蛋白质,在兔体内产生抗体(IgG)。纯化后,针对30 kDa区域蛋白质的IgG识别33 kDa的成分,但也识别分子量约为70 kDa和140 kDa的蛋白质。相反,针对140 kDa蛋白质的抗体也识别70 kDa和33 kDa的蛋白质。然而,如果在转移到硝酸纤维素膜之前,将溶解的肌膜提取物用二硫苏糖醇(DTT)处理,则看不到140 kDa的蛋白质。针对30 kDa蛋白质的抗体和针对140 kDa蛋白质的抗体都抑制了肌膜囊泡的钠/钙交换活性。有人提出,心脏肌膜钠/钙交换体的基本单位是一个分子量约为33 kDa的单体,功能活跃的交换体是一个四聚体,其中四个33 kDa的亚基通过二硫键结合在一起。在单体 - 四聚体转变过程中,还形成了一个分子量为70 kDa的中间二聚体状态。