Riley Andrew M, Dozol Helene, Spiess Bernard, Potter Barry V L
Wolfson Laboratory of Medicinal Chemistry, Department of Pharmacy and Pharmacology, University of Bath, Bath BA2 7AY, UK.
Biochem Biophys Res Commun. 2004 May 28;318(2):444-52. doi: 10.1016/j.bbrc.2004.04.051.
2-O-(2-Aminoethyl)-Ins(1,4,5)P(3), (5), a novel derivative of the Ca(2+)-mobilising second messenger d-myo-inositol 1,4,5-trisphosphate [Ins(1,4,5)P(3)], was synthesised from myo-inositol. 5 was found to be a potent mobiliser of intracellular Ca(2+), and an Ins(1,4,5)P(3) affinity matrix synthesised from 5 was effective at selectively binding N-terminal fragments of the Ins(1,4,5)P(3) receptor containing the intact Ins(1,4,5)P(3) binding site. The microprotonation scheme for 5 was resolved and the related constants were determined in comparison with Ins(1,4,5)P(3) and another reactive Ins(1,4,5)P(3) analogue 1-O-(2-aminoethyl-1-phospho)-Ins(4,5)P(2), (2a), by potentiometric and NMR titration methods. The (31)P and (1)H NMR titration curves for compound 5 and Ins(1,4,5)P(3) are remarkably close, indicating analogous acid-base properties and intramolecular interactions for the two compounds. The 1-phosphate-modified Ins(1,4,5)P(3) derivative 2a, on the contrary, behaves as a bisphosphorylated rather than a trisphosphorylated inositol. Thus, 5 is a new reactive Ins(1,4,5)P(3) analogue of considerable potential for investigation of the chemical biology of Ins(1,4,5)P(3)-mediated cellular signalling.
2 - O -(2 - 氨基乙基) - 肌醇(1,4,5)三磷酸酯(5)是钙离子动员第二信使d - 肌醇1,4,5 - 三磷酸酯[Ins(1,4,5)P(3)]的一种新型衍生物,由肌醇合成。发现5是细胞内钙离子的有效动员剂,由5合成的Ins(1,4,5)P(3)亲和基质能有效选择性结合含有完整Ins(1,4,5)P(3)结合位点的Ins(1,4,5)P(3)受体的N端片段。解析了5的微质子化方案,并通过电位滴定和核磁共振滴定法与Ins(1,4,5)P(3)及另一种反应性Ins(1,4,5)P(3)类似物1 - O -(2 - 氨基乙基 - 1 - 磷酸) - 肌醇(4,5)二磷酸酯(2a)比较确定了相关常数。化合物5和Ins(1,4,5)P(3)的³¹P和¹H核磁共振滴定曲线非常接近,表明这两种化合物具有类似的酸碱性质和分子内相互作用。相反,1 - 磷酸修饰的Ins(1,4,5)P(3)衍生物2a表现为双磷酸化而非三磷酸化的肌醇。因此,5是一种新的具有相当潜力的反应性Ins(1,4,5)P(3)类似物,可用于研究Ins(1,4,5)P(3)介导的细胞信号转导的化学生物学。