Guillou Hervé, Stephens Len R, Hawkins Phillip T
The Inositide Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge, United Kingdom.
Methods Enzymol. 2007;434:117-30. doi: 10.1016/S0076-6879(07)34007-X.
The activation of class I phosphoinositide 3-kinases (PI(3)Ks) by cell surface receptors represents the initiation of a large and complex signaling network that couples many growth factors, antigens, and inflammatory stimuli to important cellular responses, such as cell growth, survival, and movement. The most direct measurement of class I PI(3)K activity in cells is the rate of production of its lipid product, phosphatidylinositol 3,4,5-trisphosphate [PtdIns(3,4,5)P(3)]. This chapter describes in detail two approaches used to estimate the levels of PtdIns(3,4,5)P(3) in cells. One approach uses radiotracer labeling of cells, lipid extraction, deacylation, and subsequent quantitation of phosphoinositides by anion-exchange high-performance liquid chromatography. The second approach uses a novel, nonradioactive assay in which the cellular lipids are extracted, phosphoinositides are enriched through binding to a neomycin matrix, dried onto a nitrocellulose membrane, and PtdIns(3,4,5)P(3) quantified by a protein-lipid overlay approach using a GRP(1) PH domain probe.
细胞表面受体激活I类磷酸肌醇3激酶(PI(3)Ks)代表了一个庞大而复杂的信号网络的启动,该网络将许多生长因子、抗原和炎症刺激与重要的细胞反应(如细胞生长、存活和运动)联系起来。细胞中I类PI(3)K活性的最直接测量方法是其脂质产物磷脂酰肌醇3,4,5-三磷酸[PtdIns(3,4,5)P(3)]的产生速率。本章详细描述了用于估计细胞中PtdIns(3,4,5)P(3)水平的两种方法。一种方法是对细胞进行放射性示踪剂标记、脂质提取、脱酰基,然后通过阴离子交换高效液相色谱法对磷酸肌醇进行定量。第二种方法使用一种新型的非放射性检测方法,其中提取细胞脂质,通过与新霉素基质结合富集磷酸肌醇,干燥在硝酸纤维素膜上,并使用GRP(1) PH结构域探针通过蛋白质-脂质覆盖法对PtdIns(3,4,5)P(3)进行定量。