Cruz L J, Kupryszewski G, LeCheminant G W, Gray W R, Olivera B M, Rivier J
Clayton Foundation Laboratories for Peptide Biology, Salk Institute, La Jolla, California 92037.
Biochemistry. 1989 Apr 18;28(8):3437-42. doi: 10.1021/bi00434a043.
The peptide conotoxin GIIIA from Conus geographus L. venom, which specifically blocks sodium channels in muscle, has been synthesized by a solid-phase method. The three disulfide bridges were formed by air oxidation. After HPLC purification, the synthetic product was shown to be identical with the native conotoxin GIIIA from Conus geographus. A high specific activity, 125I derivative of mu-conotoxin was prepared and used for binding assays to the Na channel from Electrophorus electric organ. Specific binding could be abolished by competition with tetrodotoxin. The radiolabeled toxin was specifically cross-linked to the Na channel. These studies demonstrate that mu-conotoxin GIIIA can be used to define the guanidinium toxin binding site and will be a useful ligand for understanding functionally important differences between Na channel subtypes.
来自地纹芋螺毒液的肽类芋螺毒素GIIIA可特异性阻断肌肉中的钠通道,已通过固相法合成。三条二硫键通过空气氧化形成。经高效液相色谱纯化后,合成产物显示与来自地纹芋螺的天然芋螺毒素GIIIA相同。制备了具有高比活性的μ-芋螺毒素的125I衍生物,并用于对电鳗电器官钠通道的结合测定。与河豚毒素竞争可消除特异性结合。放射性标记的毒素可特异性交联到钠通道上。这些研究表明,μ-芋螺毒素GIIIA可用于确定胍基毒素结合位点,并且将是理解钠通道亚型之间功能重要差异的有用配体。