Li Guangpu, Qian Hong
Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Cell Biochem Biophys. 2003;39(1):45-59. doi: 10.1385/CBB:39:1:45.
Intracellular signal transduction pathways transmit signals from the cell surface to various intracellular destinations, such as cytoskeleton and nucleus through a cascade of protein-protein interactions and activation events, leading to phenotypic changes such as cell proliferation, differentiation, and death. Over the past two decades, numerous signaling proteins and signal transduction pathways have been discovered and characterized. There are two major classes of signaling proteins: phosphoproteins (e.g., mitogen-activated protein kinases) and guanosine triphosphatases (GTPases; e.g., Ras and G proteins). They both function as molecular switches by addition and removal of one or more high-energy phosphate groups. This review discusses developments that seek to quantify the signal transduction processes with kinetic analysis and mathematical modeling of the signaling phosphoproteins and GTPases. These studies have provided insights into the sensitivity and specificity amplification of biological signals in integrated systems.
细胞内信号转导通路通过一系列蛋白质-蛋白质相互作用和激活事件,将信号从细胞表面传递到各种细胞内目的地,如细胞骨架和细胞核,从而导致细胞增殖、分化和死亡等表型变化。在过去二十年中,已发现并表征了众多信号蛋白和信号转导通路。信号蛋白主要有两大类:磷蛋白(如丝裂原活化蛋白激酶)和鸟苷三磷酸酶(GTP酶;如Ras和G蛋白)。它们都通过添加和去除一个或多个高能磷酸基团来充当分子开关。本综述讨论了旨在通过对信号磷蛋白和GTP酶进行动力学分析和数学建模来量化信号转导过程的研究进展。这些研究为综合系统中生物信号的敏感性和特异性放大提供了见解。