Krauss Michael, Haucke Volker
Institute of Chemistry and Biochemistry, Department of Membrane Biochemistry, Freie Universität Berlin, Takustrasse 6, 14195 Berlin, Germany.
FEBS Lett. 2007 May 22;581(11):2105-11. doi: 10.1016/j.febslet.2007.01.089. Epub 2007 Feb 12.
Phosphoinositides serve as important spatio-temporal regulators of intracellular trafficking and cell signalling events. In addition to their recognition by specific phosphoinositide binding domains present within cytoplasmic adaptor proteins or membrane integral channels and transporters phosphoinositides may affect membrane transport by eliciting conformational changes within proteins or by regulating enzymatic activities. During adaptor-mediated membrane traffic phosphoinositides form part of coincidence detection systems that aid in targeting pools of specific phosphoinositides to select intracellular transport pathways. In this review, we discuss potential mechanisms for conferring selectivity onto the phosphoinositide code as well as possible avenues for future research.
磷酸肌醇作为细胞内运输和细胞信号传导事件的重要时空调节因子。除了通过细胞质衔接蛋白或膜整合通道及转运蛋白中存在的特定磷酸肌醇结合结构域对其进行识别外,磷酸肌醇还可能通过引发蛋白质构象变化或调节酶活性来影响膜运输。在衔接蛋白介导的膜运输过程中,磷酸肌醇构成了巧合检测系统的一部分,有助于将特定磷酸肌醇池靶向到特定的细胞内运输途径。在本综述中,我们讨论了赋予磷酸肌醇编码选择性的潜在机制以及未来研究的可能途径。