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香豆素抑制剂与胺/氨基酸激活剂与人碳酸酐酶的结合部位比较。

Binding site comparison for coumarin inhibitors and amine/amino acid activators of human carbonic anhydrases.

机构信息

Department NEUROFARBA - Pharmaceutical and nutraceutical section, University of Firenze, via Ugo Schiff 6, 50019, Sesto Fiorentino (Florence), Italy.

Chemistry Department, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Saudi Arabia.

出版信息

Eur J Med Chem. 2021 Dec 15;226:113875. doi: 10.1016/j.ejmech.2021.113875. Epub 2021 Sep 30.

DOI:10.1016/j.ejmech.2021.113875
PMID:34634741
Abstract

The first structural analysis comparing the binding mode to the target carbonic anhydrases (CAs, EC 4.2.1.1) of two opposite classes of modulators is presented here: coumarin derivatives act as prodrug CA inhibitors (CAIs), being hydrolyzed by the enzyme esterase activity to 2-hydroxycinnamic acids that occlude the active site entrance; CA activators (CAAs) belonging of the amine and amino acid types, enhance the CA activity by increasing the efficiency of the rate-determining proton shuttling step in the CA catalytic cycle. Analysis of the crystallographic data available for the human CA isoform II in adduct with two coumarin CAIs and some CAAs showed that both types of CA modulators bind in the same region of the enzyme active site, basically interacting with superimposable amino acid residues, that are Trp5, Asn62, His64, Asn67, Gln92, Thr200. A plethora of water molecules also participate in the adducts formation. This structural analysis showed that presence of certain chemical groups in the compound structure is mandatory to produce an activating rather than inhibitory action, such as multiple nitrogen- and oxygen-based moieties capable of shuttling protons or forming extended H-bond networks nearby the proton shuttle residue. This constitutes the only known example among all enzymes of an identical binding site for inhibitors and activators, which, in addition, possess significant pharmacological applications.

摘要

本文首次对两类相反的调节剂的靶碳酸酐酶(CA,EC 4.2.1.1)结合模式进行了结构分析:香豆素衍生物作为前药 CA 抑制剂(CAI),被酶酯酶活性水解为 2-羟基肉桂酸,从而封闭活性部位入口;属于胺和氨基酸类型的 CA 激活剂(CAA)通过增加 CA 催化循环中速率决定质子转移步骤的效率来增强 CA 活性。对与两种香豆素 CAI 和一些 CAA 结合的人 CA 同工型 II 的晶体学数据进行分析表明,这两种类型的 CA 调节剂都结合在酶活性部位的相同区域,基本上与可叠加的氨基酸残基相互作用,这些残基是 Trp5、Asn62、His64、Asn67、Gln92、Thr200。大量水分子也参与了加合物的形成。这种结构分析表明,化合物结构中存在某些化学基团对于产生激活作用而不是抑制作用是必需的,例如能够传递质子或在质子转移残基附近形成扩展氢键网络的多个含氮和含氧部分。这是在所有具有相同结合位点的酶中抑制剂和激活剂的唯一已知示例,此外,它们还具有重要的药理学应用。

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