Angelides K J
Biochemistry. 1981 Jul 7;20(14):4107-18. doi: 10.1021/bi00517a025.
Fluorescent and photoactivatable fluorescent derivatives of tetrodotoxin (TTX) have been synthesized. N-Methylanthraniloylglycine hydrazide, anthraniloyl hydrazide, and 2-azidoanthraniloylglycine hydrazide were coupled to the carbonyl at C6 of oxidized tetrodotoxin to form stable fluorescent hydrazones. The C6 ketone can be reductively aminated with either ammonium or methylammonium acetate to form 6-amino- or 6-(methylamino)tetrodotoxin, which can then be acylated by a variety of fluorescent reagents. The biological activity, competitive binding with [3H]tetrodotoxin for the receptor on rat axonal membranes, and equilibrium binding isotherms obtained by fluorescence enhancement or anisotropy indicate that the derivatives are only about 2-5 times less active then tetrodotoxin itself. The 2-azidoanthraniloylglycine hydrazone of oxidized tetrodotoxin, when activated by light, generates a reactive nitrene which is capable of covalent insertion into the toxin receptor. The product of the photolysis is a highly fluorescent tetrodotoxin derivative which is irreversibly linked to the receptor site. The excitation and emission spectra of the fluorescent tetrodotoxin derivatives vary with solvent polarity, and this sensitivity has been used to determine the immediate environmental characteristics of the toxin binding site of the sodium channel. It is concluded that the toxin binding site is highly polar. Emission and excitation spectra reveal that radiationless energy is transferred from tryptophan residues of the receptor to the anthraniloyl group of the TTX derivatives.
河豚毒素(TTX)的荧光和光活化荧光衍生物已被合成。N-甲基邻氨基苯甲酰甘氨酸酰肼、邻氨基苯甲酰肼和2-叠氮基邻氨基苯甲酰甘氨酸酰肼与氧化河豚毒素C6位的羰基偶联,形成稳定的荧光腙。C6酮可以用醋酸铵或醋酸甲铵进行还原胺化反应,形成6-氨基-或6-(甲基氨基)河豚毒素,然后可以用各种荧光试剂进行酰化。通过荧光增强或各向异性获得的生物活性、与大鼠轴突膜上受体的[3H]河豚毒素竞争性结合以及平衡结合等温线表明,这些衍生物的活性仅比河豚毒素本身低约2-5倍。氧化河豚毒素的2-叠氮基邻氨基苯甲酰甘氨酸腙在光激活时会产生一种活性氮烯,它能够共价插入毒素受体。光解产物是一种与受体位点不可逆连接的高荧光河豚毒素衍生物。荧光河豚毒素衍生物的激发光谱和发射光谱随溶剂极性而变化,这种敏感性已被用于确定钠通道毒素结合位点的直接环境特征。得出的结论是,毒素结合位点具有高度极性。发射光谱和激发光谱表明,无辐射能量从受体的色氨酸残基转移到TTX衍生物的邻氨基苯甲酰基。