Becker E L, Talley V, Showell H J, Naccache P H, Sha'afi R I
J Cell Biol. 1978 May;77(2):329-33. doi: 10.1083/jcb.77.2.329.
Addition of the synthetic chemotactic factor, formyl-methionyl-leucyl-phenylala-nine (F-Met-Leu-Phe) to medium containing magnesium, sodium, and potassium results in a doubling of the "Na+, K+"-ATPase activity of the plasma membrane fraction from polymophonuclear leukocytes (PMN). This activation is sensitive to ouabain inhibition and is dose dependent, maximal activity occuring at 10(-9)MF-Met-Leu-Phe. Equivalent activation was observed with the nonformylated derivative Met-Leu-Phe at 10(-9)M. The dipeptide, carbobenzoxy-methionylphenylalanine, which acts as an antagonist for F-Met-Leu-Phe, prevents the stimulation of the "Na+, K+"-ATPase by F-Met-Leu-Phe.
在含有镁、钠和钾的培养基中添加合成趋化因子甲酰甲硫氨酰亮氨酰苯丙氨酸(F-Met-Leu-Phe),会使多形核白细胞(PMN)质膜部分的“Na +,K +”-ATP酶活性加倍。这种激活对哇巴因抑制敏感且呈剂量依赖性,最大活性出现在10(-9)M F-Met-Leu-Phe时。在10(-9)M时,未甲酰化的衍生物Met-Leu-Phe也观察到了同等程度的激活。作为F-Met-Leu-Phe拮抗剂的二肽苄氧羰基甲硫氨酰苯丙氨酸可阻止F-Met-Leu-Phe对“Na +,K +”-ATP酶的刺激。