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关于钙调蛋白与D600、三氟拉嗪及其他一些疏水药物相互作用的113Cd和1H核磁共振研究。

A 113Cd and 1H NMR study of the interaction of calmodulin with D600, trifluoperazine and some other hydrophobic drugs.

作者信息

Andersson A, Drakenberg T, Thulin E, Forsén S

出版信息

Eur J Biochem. 1983 Aug 15;134(3):459-65. doi: 10.1111/j.1432-1033.1983.tb07589.x.

Abstract

The interaction of calmodulin with D600 (a methoxy derivative of verapamil), trifluoperazine and some other drugs was studied by 113Cd and 1H NMR. All four cation binding sites of calmodulin were found to be affected by the binding of the drugs to calmodulin. The physiologically active and inactive forms of felodipine were found to give qualitatively the same changes in the 113Cd NMR spectra of calmodulin. The interpretation of this observation in terms of the physiological relevance of the binding to calmodulin is discussed. The binding constants for the two strongly bound trifluoperazine molecules were found to differ by one or two orders of magnitude. A competition study showed that trifluoperazine replaces D600 from at least one binding site on calmodulin. Moreover the binding of D600 was found to be calcium dependent. The data indicate that two calcium ions bound to calmodulin are sufficient to render the binding site(s) accessible for D600.

摘要

利用113Cd和1H核磁共振研究了钙调蛋白与D600(维拉帕米的甲氧基衍生物)、三氟拉嗪及其他一些药物的相互作用。发现钙调蛋白的所有四个阳离子结合位点都受到药物与钙调蛋白结合的影响。发现非洛地平的生理活性和非活性形式在钙调蛋白的113Cd核磁共振谱中产生定性相同的变化。讨论了根据与钙调蛋白结合的生理相关性对这一观察结果的解释。发现两个紧密结合的三氟拉嗪分子的结合常数相差一到两个数量级。一项竞争研究表明,三氟拉嗪从钙调蛋白上的至少一个结合位点取代了D600。此外,发现D600的结合是钙依赖性的。数据表明,与钙调蛋白结合的两个钙离子足以使D600的结合位点可及。

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