Mathews W R, Guido D M, Huff R M
Biopolymer Chemistry, Upjohn Company, Kalamazoo, Michigan 49001.
Anal Biochem. 1988 Jan;168(1):63-70. doi: 10.1016/0003-2697(88)90010-3.
The analysis of inositol phosphates by anion-exchange HPLC is described. The method employs a citrate buffer gradient to resolve several inositol phosphates including inositol 1-phosphate, inositol 1,4-bisphosphate (IP2), and inositol 1,4,5-trisphosphate (IP3), as well as some of the isomers of these compounds. Since the buffer system does not contain any phosphate, we can use a phosphate assay to examine the chromatographic behavior of phosphate-containing compounds. The method shows good resolution and recovery (greater than 95% for IP2 and IP3). Total analysis time, including reequilibration, is about 90 min. In addition, an isocratic system that can rapidly (less than 10 min) measure IP3 is described. The HPLC system was used to characterize inositol phosphate turnover in thrombin-stimulated platelets and formylmethionyl-leucyl-phenylalanine-stimulated HL-60 cells.
本文描述了通过阴离子交换高效液相色谱法(HPLC)分析肌醇磷酸酯的方法。该方法采用柠檬酸盐缓冲液梯度来分离几种肌醇磷酸酯,包括肌醇-1-磷酸、肌醇-1,4-二磷酸(IP2)和肌醇-1,4,5-三磷酸(IP3),以及这些化合物的一些异构体。由于缓冲系统不含任何磷酸盐,我们可以使用磷酸盐测定法来检测含磷化合物的色谱行为。该方法具有良好的分离度和回收率(IP2和IP3的回收率大于95%)。包括重新平衡在内的总分析时间约为90分钟。此外,还描述了一种能够快速(少于10分钟)测量IP3的等度系统。该HPLC系统用于表征凝血酶刺激的血小板和甲酰甲硫氨酰-亮氨酰-苯丙氨酸刺激的HL-60细胞中肌醇磷酸酯的周转情况。