Liberali Prisca, Rämö Pauli, Pelkmans Lucas
Institute of Molecular Systems Biology, ETH Zurich, CH-8093 Zurich, Switzerland.
Annu Rev Cell Dev Biol. 2008;24:501-23. doi: 10.1146/annurev.cellbio.041008.145637.
The field of endocytosis is in strong need of formal biophysical modeling and mathematical analysis. At the same time, endocytosis must be much better integrated into cellular physiology to understand the former's complex behavior in such a wide range of phenotypic variations. Furthermore, the concept that endocytosis provides the space-time for signal transduction can now be experimentally addressed. In this review, we discuss these principles and argue for a systematic and top-down approach to study the endocytic membrane system. We provide a summary of published observations on protein kinases regulating endocytic machinery components and discuss global unbiased approaches to further map out kinase regulatory networks. In particular, protein phosphorylation is at the heart of controlling the physical properties of endocytosis and of integrating these physical properties into the signal transduction networks of the cell to allow a fine-tuned response to the continuously varying physiological conditions of a cell.
内吞作用领域迫切需要形式化的生物物理建模和数学分析。与此同时,内吞作用必须更好地融入细胞生理学,以理解其在如此广泛的表型变异中的复杂行为。此外,内吞作用为信号转导提供时空的概念现在可以通过实验来探讨。在这篇综述中,我们讨论这些原理,并主张采用系统的自上而下的方法来研究内吞膜系统。我们总结了已发表的关于调节内吞机制组件的蛋白激酶的观察结果,并讨论了进一步绘制激酶调控网络的全局无偏方法。特别是,蛋白质磷酸化是控制内吞作用物理特性以及将这些物理特性整合到细胞信号转导网络中以实现对细胞不断变化的生理条件进行微调反应的核心。