Srinivasan S, Shibata M, Rein R
Department of Biophysics, Roswell Park Memorial Institute, Buffalo, New York 14263.
Prog Clin Biol Res. 1987;253:171-80.
Snake toxins bind to the periphery of acetylcholine receptor which overlaps with the agonist site, thus inhibiting the ion channel opening mechanism. It has been proposed (Stroud and Finer-Moore, 1985) that the residues lying between Cys 130 and Cys 142 of the alpha-subunit of the acetylcholine receptor participate in the binding of toxins. A three-dimensional model of acetylcholine with cobratoxin and erabutoxin is built based on the interaction scheme proposed by Smart et al. (1984). The differences in the hydrogen bonding schemes between the two complexes are discussed. The results show the effect of the conservative substitution (Asp/Glu) at position 42 in the toxins on the binding interactions.
蛇毒素与乙酰胆碱受体的外周结合,该外周与激动剂位点重叠,从而抑制离子通道开放机制。有人提出(斯特劳德和芬纳 - 摩尔,1985年),乙酰胆碱受体α亚基中位于半胱氨酸130和半胱氨酸142之间的残基参与毒素的结合。基于斯马特等人(1984年)提出的相互作用方案,构建了乙酰胆碱与眼镜蛇毒素和海蛇毒素的三维模型。讨论了两种复合物之间氢键方案的差异。结果显示了毒素中第42位保守取代(天冬氨酸/谷氨酸)对结合相互作用的影响。