Bago Ruzica, Malik Nazma, Munson Michael J, Prescott Alan R, Davies Paul, Sommer Eeva, Shpiro Natalia, Ward Richard, Cross Darren, Ganley Ian G, Alessi Dario R
*MRC Protein Phosphorylation and Ubiquitylation Unit, College of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
†Division of Cell Signalling and Immunology, College of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K.
Biochem J. 2014 Nov 1;463(3):413-27. doi: 10.1042/BJ20140889.
The Vps34 (vacuolar protein sorting 34) class III PI3K (phosphoinositide 3-kinase) phosphorylates PtdIns (phosphatidylinositol) at endosomal membranes to generate PtdIns(3)P that regulates membrane trafficking processes via its ability to recruit a subset of proteins possessing PtdIns(3)P-binding PX (phox homology) and FYVE domains. In the present study, we describe a highly selective and potent inhibitor of Vps34, termed VPS34-IN1, that inhibits Vps34 with 25 nM IC50 in vitro, but does not significantly inhibit the activity of 340 protein kinases or 25 lipid kinases tested that include all isoforms of class I as well as class II PI3Ks. Administration of VPS34-IN1 to cells induces a rapid dose-dependent dispersal of a specific PtdIns(3)P-binding probe from endosome membranes, within 1 min, without affecting the ability of class I PI3K to regulate Akt. Moreover, we explored whether SGK3 (serum- and glucocorticoid-regulated kinase-3), the only protein kinase known to interact specifically with PtdIns(3)P via its N-terminal PX domain, might be controlled by Vps34. Mutations disrupting PtdIns(3)P binding ablated SGK3 kinase activity by suppressing phosphorylation of the T-loop [PDK1 (phosphoinositide-dependent kinase 1) site] and hydrophobic motif (mammalian target of rapamycin site) residues. VPS34-IN1 induced a rapid ~50-60% loss of SGK3 phosphorylation within 1 min. VPS34-IN1 did not inhibit activity of the SGK2 isoform that does not possess a PtdIns(3)P-binding PX domain. Furthermore, class I PI3K inhibitors (GDC-0941 and BKM120) that do not inhibit Vps34 suppressed SGK3 activity by ~40%. Combining VPS34-IN1 and GDC-0941 reduced SGK3 activity ~80-90%. These data suggest SGK3 phosphorylation and hence activity is controlled by two pools of PtdIns(3)P. The first is produced through phosphorylation of PtdIns by Vps34 at the endosome. The second is due to the conversion of class I PI3K product, PtdIns(3,4,5)P3 into PtdIns(3)P, via the sequential actions of the PtdIns 5-phosphatases [SHIP1/2 (Src homology 2-domain-containing inositol phosphatase 1/2)] and PtdIns 4-phosphatase [INPP4B (inositol polyphosphate 4-phosphatase type II)]. VPS34-IN1 will be a useful probe to delineate physiological roles of the Vps34. Monitoring SGK3 phosphorylation and activity could be employed as a biomarker of Vps34 activity, in an analogous manner by which Akt is used to probe cellular class I PI3K activity. Combining class I (GDC-0941) and class III (VPS34-IN1) PI3K inhibitors could be used as a strategy to better analyse the roles and regulation of the elusive class II PI3K.
III类磷脂酰肌醇3激酶(PI3K)Vps34(液泡蛋白分选蛋白34)在内体膜上使磷脂酰肌醇(PtdIns)磷酸化,生成磷脂酰肌醇-3-磷酸(PtdIns(3)P),该物质通过招募具有PtdIns(3)P结合PX(吞噬细胞氧化还原同源性)和FYVE结构域的部分蛋白质来调节膜运输过程。在本研究中,我们描述了一种Vps34的高选择性强效抑制剂,称为VPS34-IN1,它在体外以25 nM的半数抑制浓度(IC50)抑制Vps34,但对所测试的340种蛋白激酶和25种脂质激酶的活性没有显著抑制作用,这些激酶包括I类以及II类PI3K的所有亚型。将VPS34-IN1施用于细胞会在1分钟内诱导特定的PtdIns(3)P结合探针从内体膜上快速出现剂量依赖性分散,而不影响I类PI3K调节Akt的能力。此外,我们探究了血清和糖皮质激素调节激酶3(SGK3)是否受Vps34调控,SGK3是唯一已知通过其N端PX结构域与PtdIns(3)P特异性相互作用的蛋白激酶。破坏PtdIns(3)P结合的突变通过抑制T环[磷酸肌醇依赖性激酶1(PDK1)位点]和疏水基序(雷帕霉素哺乳动物靶点位点)残基的磷酸化消除了SGK3激酶活性。VPS34-IN1在1分钟内使SGK3磷酸化快速丧失约50 - 60%。VPS34-IN1不抑制不具有PtdIns(3)P结合PX结构域的SGK2亚型的活性。此外,不抑制Vps34的I类PI3K抑制剂(GDC-0941和BKM120)使SGK3活性降低约40%。联合使用VPS34-IN1和GDC-0941可使SGK3活性降低约80 - 90%。这些数据表明SGK3的磷酸化以及活性受两池PtdIns(3)P调控。第一池是通过Vps34在内体使PtdIns磷酸化产生。第二池是由于I类PI3K产物磷脂酰肌醇-3,4,5-三磷酸(PtdIns(3,4,5)P3)通过磷脂酰肌醇5-磷酸酶[含Src同源2结构域的肌醇磷酸酶1/2(SHIP1/2)]和磷脂酰肌醇4-磷酸酶[II型肌醇多磷酸4-磷酸酶(INPP4B)]的相继作用转化为PtdIns(3)P。VPS34-IN1将是描绘Vps34生理作用的有用探针。监测SGK3磷酸化和活性可作为Vps34活性的生物标志物,类似于用Akt来探测细胞I类PI3K活性的方式。联合使用I类(GDC-0941)和III类(VPS34-IN1)PI3K抑制剂可作为一种策略,以更好地分析难以捉摸的II类PI3K的作用和调控。