Anholt R R
Department of Physiology, Duke University Medical Center, Durham, North Carolina 27710.
Biochemistry. 1988 Aug 23;27(17):6464-8. doi: 10.1021/bi00417a040.
Chemosensory cilia isolated from the olfactory epithelium of Rana catesbeiana were solubilized with Lubrol PX in the presence of supplementary lipid, forskolin, and sodium fluoride. Subsequent removal of the detergent by adsorption onto Biobeads SM2 results in the formation of proteoliposomes that display forskolin- and GTP gamma S-sensitive adenylate cyclase activity. Sucrose gradient centrifugation of liposomes formed in the presence of fluorescently labeled phosphatidylcholine demonstrates association between the olfactory adenylate cyclase and the exogenously added lipid. Forskolin stimulates the enzyme in reconstituted membranes with the same potency as in native membranes (EC50 = 1-2 microM). However, GTP gamma S is 350-fold more potent in native membranes (EC50 = 4.0 +/- 0.5 nM) than in reconstituted membranes (EC50 = 1.4 +/- 0.3 microM). These studies represent a first step toward the functional reconstitution and molecular dissection of the olfactory membrane.
从牛蛙嗅上皮分离出的化学感受纤毛,在补充脂质、福斯高林和氟化钠存在的情况下,用Lubrol PX进行溶解。随后通过吸附到BioBeads SM2上去除去污剂,导致形成显示出对福斯高林和GTPγS敏感的腺苷酸环化酶活性的蛋白脂质体。在存在荧光标记磷脂酰胆碱的情况下形成的脂质体进行蔗糖梯度离心,证明嗅觉腺苷酸环化酶与外源添加的脂质之间存在关联。福斯高林刺激重组膜中的酶的效力与在天然膜中相同(EC50 = 1-2 microM)。然而,GTPγS在天然膜中(EC50 = 4.0 +/- 0.5 nM)比在重组膜中(EC50 = 1.4 +/- 0.3 microM)效力高350倍。这些研究是迈向嗅觉膜功能重组和分子剖析的第一步。