Institute of Biochemistry & Genetics, Department of Biomedicine, University of Basel, Mattenstrasse 28, 4058 Basel, Switzerland.
Chembiochem. 2012 Sep 24;13(14):2022-35. doi: 10.1002/cbic.201200089. Epub 2012 Sep 10.
Since its discovery in the late 1980s, phosphoinositide 3-kinase (PI3K), and its isoforms have arguably reached the forefront of signal transduction research. Regulation of this lipid kinase, its functions, its effectors, in short its entire signaling network, has been extensively studied. PI3K inhibitors are frequently used in biochemistry and cell biology. In addition, many pharmaceutical companies have launched drug-discovery programs to identify modulators of PI3Ks. Despite these efforts and a fairly good knowledge of the PI3K signaling network, we still have only a rudimentary picture of the signaling dynamics of PI3K and its lipid products in space and time. It is therefore essential to create and use novel biological and chemical tools to manipulate the phosphoinositide signaling network with spatial and temporal resolution. In this review, we discuss the current and potential future tools that are available and necessary to unravel the various functions of PI3K and its isoforms.
自 20 世纪 80 年代末发现以来,磷酸肌醇 3-激酶(PI3K)及其同工酶无疑已成为信号转导研究的前沿。该脂激酶的调节、功能、效应器,简而言之,其整个信号网络已得到广泛研究。PI3K 抑制剂在生物化学和细胞生物学中经常使用。此外,许多制药公司已经启动了药物发现计划,以确定 PI3Ks 的调节剂。尽管做出了这些努力,并且对 PI3K 信号网络有了相当好的了解,但我们对 PI3K 及其脂质产物在空间和时间上的信号动力学仍然只有一个初步的了解。因此,必须创建和使用新的生物和化学工具,以具有时空分辨率来操纵磷酸肌醇信号网络。在这篇综述中,我们讨论了当前和潜在的未来工具,这些工具对于揭示 PI3K 及其同工酶的各种功能是必要的。