Taylor S J, Smith J A, Exton J H
Howard Hughes Medical Institute Laboratory, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0295.
J Biol Chem. 1990 Oct 5;265(28):17150-6.
Cholate-solubilized extracts from bovine liver plasma membranes preincubated with the nonhydrolyzable GTP analog guanosine 5'-(3-O-thio)triphosphate (GTP gamma S) displayed enhanced phosphoinositide-specific phospholipase C activity compared with extracts from membranes incubated without nucleotide or with ATP or GDP analog. Resolution of the GTP gamma S-elicited activator of phospholipase C was achieved using heparin-Sepharose which bound the phospholipase C activity. Recombination of non-adsorbed extract with salt-eluted phospholipase C activity resulted in a stimulation of enzyme activity. The GTP gamma S-dependent activator was purified, on the basis of its ability to activate partially purified phospholipase C, by sequential chromatography on Q-Sepharose, Sephacryl S-300, octyl-Sepharose, and Mono Q. The presence of G-protein beta subunits and the alpha subunits of Gi1, Gi2, and Gi3 was detected, by immunoblot analysis, in Mono Q-purified phospholipase C activator preparations. Resolution of the activator from these alpha subunits was achieved by incubation with pertussis toxin in the presence of millimolar NAD+ followed by rechromatography on Mono Q. The phospholipase C activator, thus resolved from ADP-ribosylated alpha i subunits, possessed an approximate Mr of 42 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and copurified with a substoichiometric amount of beta subunit. Immunoblot analysis of fractions from the final Mono Q column revealed cross-reactivity of the 42-kDa phospholipase C activator with antipeptide antibodies raised against residues 160-169 of alpha i1 and a region of sequence common to all known G-protein alpha subunits. The 42-kDa activator was not recognized by other alpha subunit-specific or common antibodies. These findings identify the purified phospholipase C activator as a novel G-protein alpha subunit. This may represent the active subunit of the pertussis toxin-insensitive G-protein mediating receptor-stimulated phosphoinositide breakdown in mammalian liver.
与未经核苷酸预孵育或与ATP或GDP类似物预孵育的膜提取物相比,用不可水解的GTP类似物鸟苷5'-(3 - O -硫代)三磷酸(GTPγS)预孵育的牛肝质膜胆酸盐溶解提取物显示出增强的磷酸肌醇特异性磷脂酶C活性。使用结合磷脂酶C活性的肝素 - 琼脂糖实现了对GTPγS诱导的磷脂酶C激活剂的分离。未吸附提取物与盐洗脱的磷脂酶C活性的重组导致酶活性的刺激。基于其激活部分纯化的磷脂酶C的能力,通过在Q -琼脂糖、Sephacryl S - 300、辛基 - 琼脂糖和Mono Q上的连续色谱法对GTPγS依赖性激活剂进行纯化。通过免疫印迹分析,在Mono Q纯化的磷脂酶C激活剂制剂中检测到G蛋白β亚基以及Gi1、Gi2和Gi3的α亚基的存在。通过在毫摩尔NAD⁺存在下与百日咳毒素孵育,然后在Mono Q上重新色谱,从这些α亚基中分离出激活剂。由此从ADP -核糖基化的αi亚基中分离出的磷脂酶C激活剂,在十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳上的近似分子量为42 kDa,并与亚化学计量的β亚基共纯化。对最终Mono Q柱的馏分进行免疫印迹分析显示,42 kDa的磷脂酶C激活剂与针对αi1的160 - 169位残基和所有已知G蛋白α亚基共有的序列区域产生的抗肽抗体具有交叉反应性。42 kDa的激活剂未被其他α亚基特异性或通用抗体识别。这些发现将纯化的磷脂酶C激活剂鉴定为一种新型G蛋白α亚基。这可能代表了在哺乳动物肝脏中介导受体刺激的磷酸肌醇分解的百日咳毒素不敏感G蛋白的活性亚基。