Medical Research Council (MRC) Laboratory for Molecular Cell Biology, University College London (UCL), London WC1E 6BT, UK.
Medical Research Council (MRC) Laboratory for Molecular Cell Biology, University College London (UCL), London WC1E 6BT, UK.
Trends Biochem Sci. 2017 Mar;42(3):219-231. doi: 10.1016/j.tibs.2016.10.008. Epub 2016 Nov 19.
Phosphate, as a cellular energy currency, essentially drives most biochemical reactions defining living organisms, and thus its homeostasis must be tightly regulated. Investigation into the role of inositol pyrophosphates (PP-IPs) has provided a novel perspective on the regulation of phosphate homeostasis. Recent data suggest that metabolic and signaling interplay between PP-IPs, ATP, and inorganic polyphosphate (polyP) influences and is influenced by cellular phosphate homeostasis. Different studies have demonstrated that the SPX protein domain is a key component of proteins involved in phosphate metabolism. How PP-IPs control some aspects of phosphate homeostasis has become clearer with the recently acquired crystal structures of SPX domains. We review here recent studies on eukaryote phosphate homeostasis and provide insights into future research.
磷酸盐作为细胞能量货币,本质上驱动着大多数定义生物的生化反应,因此其动态平衡必须受到严格调控。对肌醇焦磷酸盐(PP-IPs)的研究为磷酸盐动态平衡的调控提供了新的视角。最近的数据表明,PP-IPs、ATP 和无机多磷酸盐(polyP)之间的代谢和信号相互作用影响并受细胞磷酸盐动态平衡的影响。不同的研究表明,SPX 蛋白结构域是涉及磷酸盐代谢的蛋白质的关键组成部分。随着最近获得的 SPX 结构域晶体结构,PP-IPs 如何控制磷酸盐动态平衡的某些方面变得更加清晰。在这里,我们回顾了真核生物磷酸盐动态平衡的最新研究,并为未来的研究提供了见解。