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非甾体抗炎药S-酮洛芬与L/D-色氨酸在磷脂膜中的相互作用的立体选择性

Stereoselectivity of Interaction of Nonsteroidal Anti-Inflammatory Drug S-Ketoprofen with L/D-Tryptophan in Phospholipid Membranes.

作者信息

Mastova Anna V, Selyutina Olga Yu, Polyakov Nikolay E

机构信息

Institute of Chemical Kinetics and Combustion, Institutskaya Str. 3, 630090 Novosibirsk, Russia.

出版信息

Membranes (Basel). 2022 Apr 24;12(5):460. doi: 10.3390/membranes12050460.

Abstract

The mechanisms of stereoselectivity of the interaction of chiral drugs with active sites of enzymes and cell receptors attract significant attention. The first reason is the difference in therapeutic activity of the enantiomers of the common drugs. Another reason is the interest in the role of chiral inversion of amino acids involved in various peptides in the development of many diseases including Alzheimer's, Parkinson's, type II diabetes, and a number of other pathological conditions. In our study we use elementary chemical process-electron transfer (ET) to simulate individual stages of ligand-receptor and enzyme-substrate interactions. In particular, previous studies of photoinduced ET in chiral donor-acceptor dyads consisting of the nonsteroidal anti-inflammatory drug (R/S)-ketoprofen and (L)-tryptophan show the stereo and spin selectivity of ET in diastereomers. The present study is devoted to the interaction of (S)-ketoprofen with L- and D-enantiomers of tryptophan in homogeneous aqueous solution and in phospholipid membranes. The study was done using the NMR technique and molecular modeling. These approaches confirm efficient penetration of ketoprofen into the lipid bilayer and binding with tryptophan molecule. The short-lived paramagnetic intermediates formed during the photoinduced ET from electron donor tryptophan to ketoprofen have been detected using the chemically induced dynamic nuclear polarization (CIDNP) technique. It was found that S-ketoprofen interacts stereoselectively with tryptophan enantiomers in the lipid membrane. The formation of the ketyl radical of ketoprofen under irradiation leads to the oxidation of membrane lipids and may be the cause of ketoprofen phototoxicity. However, in contrast to a homogeneous solution in phosphate buffer saline, where the amino acid tryptophan accelerates the photodecomposition of KP due to intramolecular hydrogen transfer, tryptophan in a lipid membrane significantly reduces the rate of photodegradation due to a reversible electron (or hydrogen) transfer reaction. The stereoselectivity in the rate of KP and lipids decomposition under UV irradiation of S-ketoprofen in the presence of tryptophan enantiomers in lipid bilayer has been detected.

摘要

手性药物与酶及细胞受体活性位点相互作用的立体选择性机制备受关注。首要原因是常见药物对映体在治疗活性上存在差异。另一个原因是人们对参与各种肽类的氨基酸手性翻转在包括阿尔茨海默病、帕金森病、II型糖尿病及许多其他病理状况等多种疾病发展过程中的作用感兴趣。在我们的研究中,我们使用基本化学过程——电子转移(ET)来模拟配体-受体和酶-底物相互作用的各个阶段。特别地,先前对由非甾体抗炎药(R/S)-酮洛芬和(L)-色氨酸组成的手性供体-受体二元体系中光诱导ET的研究表明,非对映体中ET具有立体和自旋选择性。本研究致力于(S)-酮洛芬与色氨酸的L-和D-对映体在均相水溶液和磷脂膜中的相互作用。该研究使用了核磁共振技术和分子建模。这些方法证实了酮洛芬能有效穿透脂质双层并与色氨酸分子结合。利用化学诱导动态核极化(CIDNP)技术检测到了在从电子供体色氨酸到酮洛芬的光诱导ET过程中形成的短寿命顺磁中间体。研究发现,S-酮洛芬在脂质膜中与色氨酸对映体发生立体选择性相互作用。光照下酮洛芬酮基自由基的形成会导致膜脂质氧化,这可能是酮洛芬光毒性的原因。然而,与磷酸盐缓冲盐水中的均相溶液不同,在均相溶液中氨基酸色氨酸由于分子内氢转移会加速酮洛芬的光分解,而在脂质膜中的色氨酸由于可逆的电子(或氢)转移反应会显著降低光降解速率。在脂质双层中存在色氨酸对映体的情况下,检测到了S-酮洛芬在紫外线照射下酮洛芬和脂质分解速率的立体选择性。

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