De Vries L, Elenko E, Hubler L, Jones T L, Farquhar M G
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093-0651, USA.
Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15203-8. doi: 10.1073/pnas.93.26.15203.
GAIP (G Alpha Interacting Protein) is a member of the recently described RGS (Regulators of G-protein Signaling) family that was isolated by interaction cloning with the heterotrimeric G-protein G alpha i3 and was recently shown to be a GTPase-activating protein (GAP). In AtT-20 cells stably expressing GAIP, we found that GAIP is membrane-anchored and faces the cytoplasm, because it was not released by sodium carbonate treatment but was digested by proteinase K. When Cos cells were transiently transfected with GAIP and metabolically labeled with [35S]methionine, two pools of GAIP--a soluble and a membrane-anchored pool--were found. Since the N terminus of GAIP contains a cysteine string motif and cysteine string proteins are heavily palmitoylated, we investigated the possibility that membrane-anchored GAIP might be palmitoylated. We found that after labeling with [3H]palmitic acid, the membrane-anchored pool but not the soluble pool was palmitoylated. In the yeast two-hybrid system, GAIP was found to interact specifically with members of the G alpha i subfamily, G alpha i1, G alpha i2, G alpha i3, G alpha z, and G alpha o, but not with members of other G alpha subfamilies, G alpha s, G alpha q, and G alpha 12/13. The C terminus of G alpha i3 is important for binding because a 10-aa C-terminal truncation and a point mutant of G alpha i3 showed significantly diminished interaction. GAIP interacted preferentially with the activated (GTP) form of G alpha i3, which is in keeping with its GAP activity. We conclude that GAIP is a membrane-anchored GAP with a cysteine string motif. This motif, present in cysteine string proteins found on synaptic vesicles, pancreatic zymogen granules, and chromaffin granules, suggests GAIP's possible involvement in membrane trafficking.
GAIP(Gα相互作用蛋白)是最近描述的RGS(G蛋白信号调节剂)家族的成员,它通过与异源三聚体G蛋白Gαi3的相互作用克隆而分离出来,最近被证明是一种GTP酶激活蛋白(GAP)。在稳定表达GAIP的AtT-20细胞中,我们发现GAIP是膜锚定的且面向细胞质,因为它不会被碳酸钠处理释放,但会被蛋白酶K消化。当用GAIP瞬时转染Cos细胞并用[35S]甲硫氨酸进行代谢标记时,发现了两个GAIP池——一个可溶性池和一个膜锚定池。由于GAIP的N末端包含一个半胱氨酸串基序,并且半胱氨酸串蛋白高度棕榈酰化,我们研究了膜锚定的GAIP可能被棕榈酰化的可能性。我们发现用[3H]棕榈酸标记后,膜锚定池而非可溶性池被棕榈酰化。在酵母双杂交系统中,发现GAIP与Gαi亚家族的成员Gαi1、Gαi2、Gαi3、Gαz和Gαo特异性相互作用,但不与其他Gα亚家族的成员Gαs、Gαq和Gα12/13相互作用。Gαi3的C末端对于结合很重要,因为Gαi3的10个氨基酸的C末端截短和一个点突变显示相互作用明显减弱。GAIP优先与Gαi3的活化(GTP)形式相互作用,这与其GAP活性一致。我们得出结论,GAIP是一种具有半胱氨酸串基序的膜锚定GAP。这个基序存在于突触小泡、胰腺酶原颗粒和嗜铬颗粒上发现的半胱氨酸串蛋白中,表明GAIP可能参与膜运输。