Kerr D E, Kissinger L F, Gentry L E, Purchio A F, Shoyab M
Oncogen, Seattle, Washington 98121.
Biochem Biophys Res Commun. 1987 Oct 29;148(2):776-82. doi: 10.1016/0006-291x(87)90943-0.
Phospholipid-dependent, Ca++-sensitive protein kinase (protein kinase C) is activated by phorbol esters and diacylglycerols. A series of diacylglycerols was synthesized with different substituents at positions 1 and 2 in order to expand known structure-activity relationships for these compounds with respect to binding and activating purified protein kinase C. Compounds were synthesized with saturated and unsaturated long chain fatty acyl groups at position 1 and acetyl, butyryl, or hexanoyl groups at position 2. Binding to protein kinase C correlated well with in-vitro activation of the enzyme. These diacylglycerols activated protein kinase C in an intact cellular system causing the phosphorylation of pp60c-src. This indicates that the length of the fatty acyl group at C2 is critical and that the existence of unsaturation in the fatty acyl group at C1 is not essential.
磷脂依赖性、Ca++敏感蛋白激酶(蛋白激酶C)可被佛波酯和二酰基甘油激活。为了拓展这些化合物在结合和激活纯化的蛋白激酶C方面已知的构效关系,合成了一系列在1位和2位具有不同取代基的二酰基甘油。在1位合成了具有饱和和不饱和长链脂肪酰基、在2位合成了具有乙酰基、丁酰基或己酰基的化合物。与蛋白激酶C的结合与该酶的体外激活密切相关。这些二酰基甘油在完整细胞系统中激活蛋白激酶C,导致pp60c-src磷酸化。这表明C2位脂肪酰基的长度至关重要,而C1位脂肪酰基中不饱和键的存在并非必需。