Imagawa Toshiaki, Yamamoto Tetsuya, Kaya Shunji, Sakaguchi Kazuyasu, Taniguchi Kazuya
Biochemistry, Division of Chemistry, Graduate School of Science, Hokkaido University, Nishi, Sapporo 060-0810, Japan.
J Biol Chem. 2005 May 13;280(19):18736-44. doi: 10.1074/jbc.M500137200. Epub 2005 Mar 11.
The highly conserved amino acids of rat Na,K-ATPase, Thr-774 in the transmembrane helices M5, Val-920 and Gln-923 in M8, and Glu-953 and Glu-954 in M9, the side chains of which appear to be in close proximity, were mutated, and the resulting proteins, T774A, E953A/K, and E954A/K, V920E and Q923N/E/D/L, were expressed in HeLa cells. Ouabain-resistant cell lines were obtained from T774A, V920E, E953A, and E954A, whereas Q923N/E/D/L, E953K, and E954K could only be transiently expressed as fusion proteins with an enhanced green fluorescent protein. The apparent K0.5 values for Na+, as estimated by the Na+-dependent phosphoenzyme formation (K0.5(Na,EP)) or Na,K-ATPase activity (K(0.5)(Na,ATPase)), were increased by around 2 approximately 8-fold in the case of T774A, V920E, and E954A. The apparent K0.5 values for K+, as estimated by the Na,K-ATPase (K0.5(K,ATPase)) or p-nitrophenylphosphatase activity (K0.5(K,pNPPase)), were affected only slightly by the 3 mutations, except that V920E showed a 1.7-fold increase in the K0.5(K,ATPase). The apparent K0.5 values for ATP (K0.5(EP)), as estimated by phosphorylation (a high affinity ATP effect), were increased by 1.6 approximately 2.6-fold in the case of T774A, V920E, and E954A. Those estimated by Na,K-ATPase activity (K0.5(ATPase)) and ATP-induced inhibition (K(i,0.5)(pNPPase)) of K-pNPPase activity (low affinity ATP effects) were, respectively, increased by 1.8-fold and unchanged in the case of T774A but decreased by 2- and 4.8-fold in the case of V920E and were slightly changed and increased by 1.7-fold in the case of E954A. The E953A showed little significant change in the apparent affinities. These results suggest that Gln-923 in M8 is crucial for the active transport of Na+ and/or K+ across membranes and that the side chain oxygen atom of Thr-774 in M5, the methyl group(s) of Val-920 in M8, and the carboxyl oxygen(s) of Glu-954 in M9 mainly play some role in the transport of Na+ and also in the high and low affinity ATP effects rather than the transport of K+.
大鼠钠钾ATP酶中高度保守的氨基酸,即跨膜螺旋M5中的苏氨酸 - 774、M8中的缬氨酸 - 920和谷氨酰胺 - 923以及M9中的谷氨酸 - 953和谷氨酸 - 954,它们的侧链似乎彼此靠近,对这些氨基酸进行了突变,并将产生的蛋白质T774A、E953A/K、E954A/K、V920E和Q923N/E/D/L在HeLa细胞中表达。从T774A、V920E、E953A和E954A获得了哇巴因抗性细胞系,而Q923N/E/D/L、E953K和E954K只能作为与增强型绿色荧光蛋白的融合蛋白瞬时表达。通过钠依赖性磷酸酶形成(K0.5(Na,EP))或钠钾ATP酶活性(K(0.5)(Na,ATPase))估计的Na+的表观K0.5值,在T774A、V920E和E954A的情况下增加了约2至8倍。通过钠钾ATP酶(K0.5(K,ATPase))或对硝基苯磷酸酶活性(K0.5(K,pNPPase))估计的K+的表观K0.5值,除V920E的K0.5(K,ATPase)增加了1.7倍外,这3种突变对其影响很小。通过磷酸化(高亲和力ATP效应)估计的ATP的表观K0.5值(K0.5(EP)),在T774A、V920E和E954A的情况下增加了1.6至2.6倍。通过钠钾ATP酶活性(K0.5(ATPase))和ATP对K - pNPPase活性的抑制(K(i,0.5)(pNPPase))(低亲和力ATP效应)估计的那些值,在T774A的情况下分别增加了1.8倍且没有变化,但在V920E的情况下分别降低了2倍和4.8倍,在E954A的情况下略有变化并增加了1.7倍。E953A在表观亲和力方面几乎没有显著变化。这些结果表明,M8中的谷氨酰胺 - 923对于Na+和/或K+跨膜的主动转运至关重要,并且M5中的苏氨酸 - 774的侧链氧原子、M8中的缬氨酸 - 920的甲基以及M9中的谷氨酸 - 954的羧基氧主要在Na+的转运以及高亲和力和低亲和力ATP效应中起作用,而不是在K+的转运中起作用。