摘要
目的:寻找猪血小板中蛋白激酶CK2可能的天然底物。方法:以[γ-32P]GTP为磷酸供体,用精胺激活蛋白激酶CK2和用肝素抑制蛋白激酶CK2活性,然后用放射自显影的方法检测底物蛋白磷酸化。结果:精胺可增加17.4kD蛋白磷酸化;肝素能完全抑制43kD和66kD底物蛋白磷酸化,肝素还增加39.4kD底物磷酸化。结论:猪血小板中17.4kD。
Objective:To search for natural substrates of protein kinase CK2 in pig platelets.Methods:[γ 32 P]GTP was used as phosphate donor.Activity of protein kinase CK2 was stimulated by spermine and was inhibited by heparin. Protein phosphorylation was detected by autoradiography.Results:Spermine induced 17.4kD polypeptide phosphorylation;heparin completely inhibited 43kD and 66kD polypeptide phosphorylation and also induced 39.4kD polypeptide phosphorylation.Conclusion:17.4kD、43kD and 66kD proteins may be natural substrates of protein kinase CK2 in pig platelets.
出处
《广东医学院学报》
1998年第1期17-18,共2页
Journal of Guangdong Medical College
基金
广东省重点学科基金
关键词
蛋白激酶CK2
底物
蛋白磷酸化
血小板
protein kinase CK2
substrate
protein phosphorylation
platelet