Vilsen B, Andersen J P, MacLennan D H
Danish Biomembrane Research Centre, Institute of Physiology, University of Aarhus.
J Biol Chem. 1991 Oct 5;266(28):18839-45.
Site-specific mutagenesis was used to investigate the functional roles of amino acids in the relatively hydrophobic sequence Ile-Thr-Thr-Cys-Leu-Ala-320, located at the M4S4 boundary of the sarcomplasmic reticulum Ca(2+)-ATPase. Each of the residues was replaced with either a less hydrophogic, a polar, or a charged residue. Mutants Ile-315----Arg and Leu-319----Arg were devoid of any Ca2+ transport function or ATPase activity, while the mutant Thr-317----Asp retained about 5 and 7% of the wild-type Ca2+ transport and ATPase activities, respectively. These three mutants were able to form the ADP-sensitive phosphoenzyme intermediate (E1P) by reaction with ATP, but this intermediate decayed very slowly to the ADP-insensitive phosphoenzyme intermediate (E2P). In the mutants Ile-315----Arg and Leu-319----Arg, the level of E2P formed in the backward reaction with inorganic phosphate was extremely low, but hydrolysis of E2P occurred at a normal rate. These mutants, in addition, displayed a higher apparent affinity for Ca2+ than the wild-type enzyme. In the mutants Ile-315----Ser and Ile-315----Asp, the Ca2+ transport and ATPase activities were moderately reduced to 30-40% of the wild-type activities, but normal affinities for Ca2+, Pi, and ATP were retained, as was the low affinity modulatory effect of ATP. Mutation of Thr-316 to Asp, Thr-317 to Ala, Cys-318 to Ala and Ala-320 to Arg had little or no effect on Ca2+ transport or ATPase activities. Introduction of two negative and one positive charge by triple mutation of the Ile-Thr-Thr-317 sequence created a mutant enzyme that, although completely inactive, was inserted into the membrane, consistent with a location of these residues on the cytoplasmic side of the M4S4 interface. Our findings suggest that the amphipathic character of the S4 helix and/or the distribution of charges in S4 is important for the stability of the E2P intermediate.
位点特异性诱变被用于研究位于肌浆网Ca(2+)-ATP酶M4S4边界的相对疏水序列Ile-Thr-Thr-Cys-Leu-Ala-320中氨基酸的功能作用。每个残基都被替换为疏水性更低、极性或带电荷的残基。突变体Ile-315----Arg和Leu-319----Arg丧失了任何Ca2+转运功能或ATP酶活性,而突变体Thr-317----Asp分别保留了约5%和7%的野生型Ca2+转运和ATP酶活性。这三个突变体能够通过与ATP反应形成ADP敏感的磷酸化酶中间体(E1P),但该中间体向ADP不敏感的磷酸化酶中间体(E2P)的衰减非常缓慢。在突变体Ile-315----Arg和Leu-319----Arg中,与无机磷酸盐的逆向反应中形成的E2P水平极低,但E2P的水解以正常速率发生。此外,这些突变体对Ca2+的表观亲和力高于野生型酶。在突变体Ile-315----Ser和Ile-315----Asp中,Ca2+转运和ATP酶活性适度降低至野生型活性的30-40%,但对Ca2+、Pi和ATP的正常亲和力得以保留,ATP的低亲和力调节作用也得以保留。Thr-316突变为Asp、Thr-317突变为Ala、Cys-318突变为Ala以及Ala-320突变为Arg对Ca2+转运或ATP酶活性几乎没有影响。通过Ile-Thr-Thr-317序列的三重突变引入两个负电荷和一个正电荷产生了一种突变酶,尽管其完全无活性,但被插入到膜中,这与这些残基位于M4S4界面的细胞质一侧一致。我们的研究结果表明,S4螺旋的两亲性特征和/或S4中的电荷分布对于E2P中间体的稳定性很重要。