Davis A
Eur J Pharmacol. 1984 Oct 30;106(1):159-65. doi: 10.1016/0014-2999(84)90690-3.
[3H]3-Cyanoimipramine has been characterised as a pseudoirreversible ligand at imipramine binding sites making it useful for molecular characterisation studies. Using this ligand, I now report that it is possible to solubilise the binding site molecule with cholate. Gel permeation chromatography on a Sepharose 4B column equilibrated in 0.1% cholate revealed a micellar size of 4.1 nm. Subsequent removal of cholate (from an initial concentration of 2% to less than 0.02%) in the presence of Azolectin (soybean lipid extract) led to reconstituted material that could be retained on glass fibre filters. Electron microscopy revealed apparent micelles of approximately 1 micron diameter. Over 16% of the original, membrane-bound, binding sites were recovered in the reconstituted material along with a similar percentage of the protein. This reconstituted material was moderately stable for up to 3 days after its preparation.
[3H]3-氰基丙咪嗪已被表征为丙咪嗪结合位点的一种假不可逆配体,这使其在分子表征研究中很有用。使用这种配体,我现在报告,用胆酸盐可以使结合位点分子增溶。在0.1%胆酸盐中平衡的琼脂糖4B柱上进行凝胶渗透色谱分析,显示胶束大小为4.1纳米。随后在大豆脂质提取物Azolectin存在的情况下,将胆酸盐从初始浓度2%去除至低于0.02%,得到了可保留在玻璃纤维滤器上的重组物质。电子显微镜显示直径约为1微米的明显胶束。在重组物质中回收了超过16%的原始膜结合结合位点以及相似比例的蛋白质。这种重组物质在制备后长达3天内具有适度的稳定性。