Kao P N, James-Kracke M R, Kao C Y
Pflugers Arch. 1983 Aug;398(3):199-203. doi: 10.1007/BF00657151.
The relative potencies of saxitoxin at pH 7.25 and 8.25 have been determined on the squid giant axon under voltage-clamp conditions or by Vmax of the propagated action potential. Of the two guanidinium groups in saxitoxin, the 7, 8, 9 group has been identified as the biologically active group. The evidence lies in the demonstration of a quantitative agreement between the relative abundance of the protonated, positively charged form of that group at pH's 7.25 and 8.25 (ratio 1.80) with the relative potencies (ratio 1.79) of the toxin. The 1, 2, 3 group is excluded by the lack of agreement between the relative abundance of the protonated form (ratio 1.00) and the relative potencies at these pH's. The 1, 2, 3 group is further excluded by the observation that neosaxitoxin is equally potent at pH 6.50 and 7.25, in spite of a difference of 6-fold in the abundance of a deprotonated hydroxyl group on N-1 which should have influenced the potency.
在电压钳制条件下,或通过传播动作电位的最大速率,已测定了在pH值7.25和8.25时石房蛤毒素的相对效价。在石房蛤毒素的两个胍基中,7、8、9基团已被确定为生物活性基团。证据在于,该基团在pH值7.25和8.25时质子化、带正电荷形式的相对丰度(比率为1.80)与毒素的相对效价(比率为1.79)之间呈现出定量一致性。由于质子化形式的相对丰度(比率为1.00)与这些pH值下的相对效价之间缺乏一致性,1、2、3基团被排除在外。尽管N-1上未质子化羟基的丰度相差6倍,而这应该会影响效价,但新石房蛤毒素在pH值6.50和7.25时的效价相同,这一观察结果进一步排除了1、2、3基团。