Massenburg D, Han J S, Liyanage M, Patton W A, Rhee S G, Moss J, Vaughan M
Laboratory of Cellular Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11718-22. doi: 10.1073/pnas.91.24.11718.
Two major forms of phospholipase D (PLD) activity, solubilized from rat brain membranes with Triton X-100, were separated by HPLC on a heparin-5PW column with buffer containing octyl glucoside. One form was completely dependent on sodium oleate for activity. The other, which was dramatically activated by the addition of ADP-ribosylation factor (ARF) 1 and guanine 5' [gamma-thio]triphosphate, required the presence of phosphatidylinositol 4,5-bisphosphate in the phosphatidylcholine substrate for demonstration of activity, as described by others. Oleate-dependent activity was unaffected by guanine 5' [gamma-thio]triphosphate, or phosphatidylinositol 4,5-bisphosphate. Both sodium oleate-and ARF-dependent activities catalyzed transphosphatidylation, thus identifying them as PLDs. ARF-dependent PLD was activated by recombinant ARF5 (class II) and ARF6 (class III), as well as ARF1 (class I). Myristoylated recombinant ARFs were more effective than their nonmyristoylated counterparts. ARFs were originally identified as activators of cholera toxin ADP-ribosyltransferase activity. The effects of recombinant ARF proteins from the three classes on cholera toxin activity (assayed under conditions identical to those used to assay PLD activity) did not, however, correlate with those on PLD, consistent with the notion that different aspects of ARF structure are involved in the two functions.
用Triton X-100从大鼠脑膜中溶解出来的磷脂酶D(PLD)活性的两种主要形式,通过在含辛基葡糖苷的缓冲液中,在肝素-5PW柱上进行高效液相色谱(HPLC)分离。一种形式的活性完全依赖于油酸钠。另一种形式,在加入ADP-核糖基化因子(ARF)1和鸟嘌呤5'-[γ-硫代]三磷酸后被显著激活,如其他人所描述的,其在磷脂酰胆碱底物中需要磷脂酰肌醇4,5-二磷酸的存在才能表现出活性。依赖油酸盐的活性不受鸟嘌呤5'-[γ-硫代]三磷酸或磷脂酰肌醇4,5-二磷酸的影响。油酸钠依赖性和ARF依赖性活性都催化转磷脂酰基反应,因此将它们鉴定为PLD。ARF依赖性PLD被重组ARF5(II类)和ARF6(III类)以及ARF1(I类)激活。肉豆蔻酰化的重组ARF比未肉豆蔻酰化的更有效。ARF最初被鉴定为霍乱毒素ADP-核糖基转移酶活性的激活剂。然而,来自这三类的重组ARF蛋白对霍乱毒素活性的影响(在与用于测定PLD活性相同的条件下测定)与对PLD的影响不相关,这与ARF结构的不同方面参与这两种功能的观点一致。