Hepler J R, Biddlecome G H, Kleuss C, Camp L A, Hofmann S L, Ross E M, Gilman A G
Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas 75235, USA.
J Biol Chem. 1996 Jan 5;271(1):496-504. doi: 10.1074/jbc.271.1.496.
Gq alpha is palmitoylated at residues Cys9 and Cys10. Removal of palmitate from purified Gq alpha with palmitoylthioesterase in vitro failed to alter interactions of Gq alpha with phospholipase C-beta 1, the G protein beta gamma subunit complex, or m1 muscarinic cholinergic receptors. Mutants C9A, C10A, C9A/C10A, C9S/C10S, and truncated Gq alpha (removal of residues 1-6) were synthesized in Sf9 cells and purified. Loss of both Cys residues or truncation prevented palmitoylation of Gq alpha. However, truncated Gq alpha and the single Cys mutants activated phospholipase C-beta 1 normally, while the double Cys mutants were poor activators. Loss of both Cys residues impaired but did not abolish interaction of Gq alpha with m1 receptors. These Cys residues are thus important regardless of their state of palmitoylation. When expressed in HEK-293 or Sf9 cells, all of the proteins studied associated entirely or predominantly with membranes, although a minor fraction of nonpalmitoylated Gq alpha proteins accumulated in the cytosol of HEK-293 cells. When subjected to TX-114 phase partitioning, a significant fraction of all of the proteins, including those with no palmitate, was found in the detergent-rich phase. Removal of residues 1-34 of Gq alpha caused a loss of surface hydrophobicity as evidenced by complete partitioning into the aqueous phase. The Cys residues at the amino terminus of Gq alpha are thus important for its interactions with effector and receptor, and the amino terminus conveys a hydrophobic character to the protein distinct from that contributed by palmitate.
Gqα在半胱氨酸9和半胱氨酸10位点被棕榈酰化。在体外使用棕榈酰硫酯酶从纯化的Gqα上去除棕榈酸酯,未能改变Gqα与磷脂酶C-β1、G蛋白βγ亚基复合物或m1毒蕈碱胆碱能受体之间的相互作用。在Sf9细胞中合成并纯化了突变体C9A、C10A、C9A/C10A、C9S/C10S以及截短的Gqα(去除第1至6位残基)。两个半胱氨酸残基的缺失或截短阻止了Gqα的棕榈酰化。然而,截短的Gqα和单个半胱氨酸突变体正常激活磷脂酶C-β1,而双半胱氨酸突变体则是较差的激活剂。两个半胱氨酸残基的缺失损害但并未消除Gqα与m1受体的相互作用。因此,无论其棕榈酰化状态如何,这些半胱氨酸残基都很重要。当在HEK-293或Sf9细胞中表达时,所有研究的蛋白质都全部或主要与膜相关,尽管一小部分未棕榈酰化的Gqα蛋白在HEK-293细胞的细胞质中积累。当进行TX-114相分配时,所有蛋白质中相当一部分,包括那些没有棕榈酸酯的蛋白质,都存在于富含去污剂的相中。去除Gqα的第1至34位残基导致表面疏水性丧失,这通过完全分配到水相中得到证明。因此,Gqα氨基末端的半胱氨酸残基对于其与效应器和受体的相互作用很重要,并且氨基末端赋予蛋白质一种不同于棕榈酸酯所贡献的疏水性特征。