Mancini J A, Abramovitz M, Cox M E, Wong E, Charleson S, Perrier H, Wang Z, Prasit P, Vickers P J
Department of Pharmacology, Merck Frosst Centre for Therapeutic Research, Quebec, Canada.
FEBS Lett. 1993 Mar 8;318(3):277-81. doi: 10.1016/0014-5793(93)80528-3.
5-Lipoxygenase-activating protein (FLAP) is an 18-kDa integral membrane protein which is essential for cellular leukotriene (LT) synthesis, and is the target of LT biosynthesis inhibitors. However, the mechanism by which FLAP activates 5-LO has not been determined. We have expressed high levels of human FLAP in Spodoptera frugiperda (Sf9) insect cells infected with recombinant baculovirus, and used this system to demonstrate that FLAP specifically binds [125I]L-739,059, a novel photoaffinity analog of arachidonic acid. This binding is inhibited by both arachidonic acid and MK-886, an LT biosynthesis inhibitor which specifically interacts with FLAP. These studies suggest that FLAP may activate 5-LO by specifically binding arachidonic acid and transferring this substrate to the enzyme.
5-脂氧合酶激活蛋白(FLAP)是一种18 kDa的整合膜蛋白,对细胞白三烯(LT)合成至关重要,并且是LT生物合成抑制剂的作用靶点。然而,FLAP激活5-脂氧合酶(5-LO)的机制尚未确定。我们已在感染重组杆状病毒的草地贪夜蛾(Sf9)昆虫细胞中高水平表达人FLAP,并利用该系统证明FLAP特异性结合[125I]L-739,059,一种新型花生四烯酸光亲和类似物。花生四烯酸和MK-886(一种与FLAP特异性相互作用的LT生物合成抑制剂)均可抑制这种结合。这些研究表明,FLAP可能通过特异性结合花生四烯酸并将该底物转移至酶来激活5-LO。