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毒蕈碱受体拮抗剂复合物的异构化

Isomerization of the muscarinic receptor . antagonist complex.

作者信息

Järv J, Hedlund B, Bartfai T

出版信息

J Biol Chem. 1979 Jul 10;254(13):5595-8.

PMID:447668
Abstract

The mechanism of binding of two antagonists, 3-quinuclidinyl benzilate and N-methyl-4-piperidinyl benzilate, to the muscarinic receptor was studied. The pseudo-first order rate constant of association showed a hyperbolic dependence on the concentration of the antagonist(s) indicating that the interaction involves two equilibria. The first binding equilibrium is reached rapidly and is characterized by dissociation constants 2.7 +/- 0.4 nM and 6.7 +/- 2.5 nM in phosphate buffer (0.05 M, pH = 7.4) for 3-quinuclidinyl benzilate and N-methyl-4-piperidinyl benzilate, respectively. The first binding equilibrium is followed by a slower isomerization step of the receptor . antagonist complex. The equilibrium constants for the isomerization step of the complex for both ligands were about 0.15. The overall constant of binding obtained as the product of the above constants shows good agreement with the results of equilibrium binding studies.

摘要

研究了两种拮抗剂,即3-奎宁环基苯甲酸酯和N-甲基-4-哌啶基苯甲酸酯与毒蕈碱受体的结合机制。缔合的准一级速率常数显示出对拮抗剂浓度的双曲线依赖性,表明这种相互作用涉及两个平衡。第一个结合平衡迅速达到,在磷酸盐缓冲液(0.05M,pH = 7.4)中,3-奎宁环基苯甲酸酯和N-甲基-4-哌啶基苯甲酸酯的解离常数分别为2.7±0.4 nM和6.7±2.5 nM。第一个结合平衡之后是受体-拮抗剂复合物较慢的异构化步骤。两种配体复合物异构化步骤的平衡常数约为0.15。作为上述常数的乘积获得的总体结合常数与平衡结合研究的结果显示出良好的一致性。

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