Department of Biochemistry and Structural Biology, Lund University, Lund, Sweden.
Vitam Horm. 2020;112:95-117. doi: 10.1016/bs.vh.2019.08.002. Epub 2019 Sep 13.
Human Aquaporin 2 (AQP2) is a membrane-bound water channel found in the kidney collecting duct whose regulation by trafficking plays a key role in regulating urine volume. AQP2 trafficking is tightly controlled by the pituitary hormone arginine vasopressin (AVP), which stimulates translocation of AQP2 residing in storage vesicles to the apical membrane. The AVP-dependent translocation of AQP2 to and from the apical membrane is controlled by multiple phosphorylation sites in the AQP2 C-terminus, the phosphorylation of which alters its affinity to proteins within the cellular membrane protein trafficking machinery. The aim of this chapter is to provide a summary of what is currently known about AVP-mediated AQP2 trafficking, dissecting the roles of individual phosphorylation sites, kinases and phosphatases and interacting proteins. From this, the picture of an immensely complex process emerges, of which many structural and molecular details remains to be elucidated.
人水通道蛋白 2(AQP2)是一种位于肾脏集合管的膜结合水通道,其通过运输的调节在调节尿量方面起着关键作用。AQP2 的运输受垂体激素精氨酸加压素(AVP)的严格控制,AVP 刺激驻留在储存小泡中的 AQP2 易位到顶端膜。AVP 依赖性 AQP2 从顶端膜的易位和返回是由 AQP2 C 末端的多个磷酸化位点控制的,其磷酸化改变了它与细胞内膜蛋白运输机制中的蛋白质的亲和力。本章的目的是提供对 AVP 介导的 AQP2 运输的当前认识的总结,剖析各个磷酸化位点、激酶和磷酸酶以及相互作用蛋白的作用。由此,一个极其复杂的过程的画面出现了,其中许多结构和分子细节仍有待阐明。