Adamo H P, Verma A K, Sanders M A, Heim R, Salisbury J L, Wieben E D, Penniston J T
Mayo Foundation, Department of Biochemistry and Molecular Biology, Rochester, MN 55905.
Biochem J. 1992 Aug 1;285 ( Pt 3)(Pt 3):791-7. doi: 10.1042/bj2850791.
A full-length cDNA corresponding to the hPMCA4 plasma membrane Ca2+ pump was assembled and expressed in COS-1 cells. The original sequence of hPMCA4 gave a very low expression. The mutation of the initiation translation site of this sequence to the consensus A/G-X-X-AUG-G increased the production of the protein. The Ca2+ pump activity in transfected cells was 1.5-3.5-fold higher than in controls. The Ca(2+)-dependence and the calmodulin stimulation of hPMCA4 expressed in COS-1 cells were comparable with those of the erythrocyte Ca2+ pump. Immunohistochemistry experiments showed that most of the expressed protein remained in intracellular membranes. Possible explanations for this targeting of the pump are discussed.
构建了与hPMCA4质膜Ca2+泵对应的全长cDNA,并在COS-1细胞中进行表达。hPMCA4的原始序列表达水平很低。将该序列的起始翻译位点突变为一致序列A/G-X-X-AUG-G后,蛋白质产量增加。转染细胞中的Ca2+泵活性比对照高1.5至3.5倍。在COS-1细胞中表达的hPMCA4的Ca(2+)依赖性和钙调蛋白刺激作用与红细胞Ca2+泵相当。免疫组织化学实验表明,大多数表达的蛋白质保留在细胞内膜中。文中讨论了该泵这种靶向定位的可能解释。