Sprague Brian L, McNally James G
Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, MD 20892, USA.
Trends Cell Biol. 2005 Feb;15(2):84-91. doi: 10.1016/j.tcb.2004.12.001.
Dynamic molecular interactions are fundamental to all cellular processes. In vivo analyses of these interactions are frequently done using fluorescence recovery after photobleaching (FRAP). Proper interpretation of FRAP data yields information about the binding interactions of fluorescently tagged molecules, including the number of binding states and the binding strength of each state. This binding information can be gleaned from appropriate models of the process underlying a FRAP recovery. Continued application and development of these approaches promise to provide crucial information for a quantitative description of the molecular networks that regulate cellular function.
动态分子相互作用是所有细胞过程的基础。对这些相互作用的体内分析通常使用光漂白后荧光恢复(FRAP)技术来完成。对FRAP数据的正确解读可得出有关荧光标记分子结合相互作用的信息,包括结合状态的数量以及每种状态的结合强度。这种结合信息可以从FRAP恢复过程的适当模型中获取。这些方法的持续应用和发展有望为定量描述调节细胞功能的分子网络提供关键信息。