Subramanian Preeti, Vora Mohsin, Gentile Luciana B, Stahelin Robert V, Chalfant Charles E
Department of Biochemistry, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA 23298-0614, USA.
J Lipid Res. 2007 Dec;48(12):2701-8. doi: 10.1194/jlr.M700356-JLR200. Epub 2007 Sep 21.
Previously, ceramide-1-phosphate (C1P) and phosphatidylinositol-4,5-bisphosphate [PI(4,5)P2] were demonstrated to be potent and specific activators of group IVA cytosolic phospholipase A2 (cPLA2alpha). In this study, we hypothesized that these anionic lipids functionally activated the enzyme by distinctly different mechanisms. Indeed, surface plasmon resonance and surface dilution kinetics demonstrated that C1P was a more potent effector than PI(4,5)P2 in decreasing the dissociation constant of the cPLA2alpha-phosphatidylcholine (PC) interaction and increasing the residence time of the enzyme on the vesicles/micelles. PI(4,5)P2, in contrast to C1P, decreased the Michaelis-Menten constant, increasing the catalytic efficiency of the enzyme. Furthermore, PI(4,5)P2 activated cPLA2alpha with a stoichiometry of 1:1 versus C1P at 2.4:1. Lastly, PI(4,5)P2, but not C1P, increased the penetration ability of cPLA2alpha into PC-rich membranes. Therefore, this study demonstrates two distinct mechanisms for the activation of cPLA2alpha by anionic lipids. First, C1P activates cPLA2alpha by increasing the residence time of the enzyme on membranes. Second, PI(4,5)P2 activates the enzyme by increasing catalytic efficiency through increased membrane penetration.
此前,已证实神经酰胺 -1-磷酸(C1P)和磷脂酰肌醇 -4,5-二磷酸[PI(4,5)P2]是IVA型胞质磷脂酶A2(cPLA2α)的强效特异性激活剂。在本研究中,我们假设这些阴离子脂质通过截然不同的机制在功能上激活该酶。事实上,表面等离子体共振和表面稀释动力学表明,在降低cPLA2α与磷脂酰胆碱(PC)相互作用的解离常数以及增加该酶在囊泡/微团上的停留时间方面,C1P比PI(4,5)P2是更有效的效应物。相比之下,PI(4,5)P2降低了米氏常数,提高了该酶的催化效率。此外,PI(4,5)P2以1:1的化学计量比激活cPLA2α,而C1P的化学计量比为2.4:1。最后,PI(4,5)P2而非C1P增加了cPLA2α进入富含PC的膜的穿透能力。因此,本研究证明了阴离子脂质激活cPLA2α的两种不同机制。第一,C1P通过增加该酶在膜上的停留时间来激活cPLA2α。第二,PI(4,5)P2通过增加膜穿透来提高催化效率从而激活该酶。