Autry J M, Jones L R
Department of Medicine and the Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
J Biol Chem. 1997 Jun 20;272(25):15872-80. doi: 10.1074/jbc.272.25.15872.
The utility of the baculovirus cell expression system for investigating Ca2+-ATPase and phospholamban regulatory interactions was examined. cDNA encoding the canine cardiac sarco(endo)plasmic Ca2+-ATPase pump (SERCA2a) was cloned for the first time and expressed in the presence and absence of phospholamban in Spodoptera frugiperda (Sf21) insect cells. The recombinant Ca2+ pump was produced in high yield, contributing 20% of the total membrane protein in Sf21 microsomes. At least 70% of the expressed pumps were active. Co-expression of wild-type, pentameric phospholamban with the Ca2+-ATPase decreased the apparent affinity of the ATPase for Ca2+, but had no effect on the maximum velocity of the enzyme, similar to phospholamban's action in cardiac sarcoplasmic reticulum vesicles. To investigate the importance of the oligomeric structure of phospholamban in ATPase regulation, SERCA2a was co-expressed with a monomeric mutant of phospholamban, in which leucine residue 37 was changed to alanine. Surprisingly, monomeric phospholamban suppressed SERCA2a Ca2+ affinity more strongly than did wild-type phospholamban, demonstrating that the pentamer is not essential for Ca2+ pump inhibition and that the monomer is the more active species. To test if phospholamban functions as a Ca2+ channel, Sf21 microsomes expressing either SERCA2a or SERCA2a plus phospholamban were actively loaded with Ca2+ and then assayed for unidirectional 45Ca2+ efflux. No evidence for a Ca2+ channel activity of phospholamban was obtained. We conclude that the phospholamban monomer is an important regulatory component inhibiting SERCA2a in cardiac sarcoplasmic reticulum membranes, and that the channel activity of phospholamban previously observed in planar bilayers is not involved in the mechanism of ATPase regulation.
研究了杆状病毒细胞表达系统在研究Ca2 + -ATP酶和受磷蛋白调节相互作用方面的实用性。首次克隆了编码犬心肌肌浆网Ca2 + -ATP酶泵(SERCA2a)的cDNA,并在草地贪夜蛾(Sf21)昆虫细胞中在有和没有受磷蛋白的情况下进行表达。重组Ca2 +泵高产,占Sf21微粒体总膜蛋白的20%。至少70%的表达泵具有活性。野生型五聚体受磷蛋白与Ca2 + -ATP酶的共表达降低了ATP酶对Ca2 +的表观亲和力,但对酶的最大速度没有影响,这与受磷蛋白在心肌肌浆网囊泡中的作用相似。为了研究受磷蛋白的寡聚结构在ATP酶调节中的重要性,SERCA2a与受磷蛋白的单体突变体共表达,其中亮氨酸残基37变为丙氨酸。令人惊讶的是,单体受磷蛋白比野生型受磷蛋白更强烈地抑制SERCA2a的Ca2 +亲和力,表明五聚体对于Ca2 +泵抑制不是必需的,并且单体是更具活性的物种。为了测试受磷蛋白是否作为Ca2 +通道起作用,将表达SERCA2a或SERCA2a加受磷蛋白的Sf21微粒体主动加载Ca2 +,然后测定单向45Ca2 +流出。没有获得受磷蛋白具有Ca2 +通道活性的证据。我们得出结论,受磷蛋白单体是抑制心肌肌浆网膜中SERCA2a的重要调节成分,并且先前在平面双层中观察到的受磷蛋白的通道活性不参与ATP酶调节机制。