Wu Mingxuan, Dul Barbara E, Trevisan Alexandra J, Fiedler Dorothea
Department of Chemistry, Princeton University, Washington Rd., 85 Princeton, NJ, 08544, USA. Tel: +1 609 258 1025.
Chem Sci. 2013 Jan;4(1):405-410. doi: 10.1039/C2SC21553E.
The diphosphoinositol polyphosphates (PP-IPs) are a central group of eukaryotic second messengers. They regulate numerous processes, including cellular energy homeostasis and adaptation to environmental stresses. To date, most of the molecular details in PP-IP signalling have remained elusive, due to a lack of appropriate methods and reagents. Here we describe the expedient synthesis of methylene-bisphosphonate PP-IP analogues. Their characterization revealed that the analogues exhibit significant stability and mimic their natural counterparts very well. This was further confirmed in two independent biochemical assays, in which our analogues potently inhibited phosphorylation of the protein kinase Akt and hydrolytic activity of the Ddp1 phosphohydrolase. The non-hydrolysable PP-IPs thus emerge as important tools and hold great promise for a variety of applications.
二磷酸肌醇多磷酸(PP-IPs)是真核生物第二信使的核心基团。它们调节众多过程,包括细胞能量稳态和对环境压力的适应。迄今为止,由于缺乏合适的方法和试剂,PP-IP信号传导中的大多数分子细节仍不清楚。在这里,我们描述了亚甲基双膦酸酯PP-IP类似物的便捷合成。它们的表征表明,这些类似物具有显著的稳定性,并且能很好地模拟其天然对应物。这在两项独立的生化分析中得到了进一步证实,在这些分析中,我们的类似物有效地抑制了蛋白激酶Akt的磷酸化和Ddp1磷酸水解酶的水解活性。因此,不可水解的PP-IPs成为重要工具,并在各种应用中具有巨大潜力。