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基于钌的含唑配体 CO 释放分子:与蛋白质的相互作用及 X 射线晶体学揭示的 CO 释放机制。

Ru-Based CO releasing molecules with azole ligands: interaction with proteins and the CO release mechanism disclosed by X-ray crystallography.

机构信息

Department of Chemical Sciences, University of Naples Federico II, Complesso Universitario di Monte Sant' Angelo, Via Cinthia, I-80126, Napoli, Italy.

Department of Chemistry, University of Florence, Via della Lastruccia 3, 50019, Sesto Fiorentino, Italy.

出版信息

Dalton Trans. 2017 Jul 25;46(29):9621-9629. doi: 10.1039/c7dt01991b.

Abstract

fac-[Ru(CO)Cl(N-Imidazole)] (RuIM), fac-[Ru(CO)Cl(N-methyl-imidazole)] (RuMIM) and fac-[Ru(CO)Cl(N-methyl-benzimidazole)] (RuMBI) are three ruthenium based CO releasing molecules (Ru-CORMs) that are cytotoxic towards ovarian and colon carcinoma cell lines. Detailed structural information on the adducts formed upon reaction of RuIM and RuMIM with hen egg white lysozyme and of the three Ru-CORMs with bovine pancreatic ribonuclease is provided here by X-ray crystallography. Comparative analysis of seven crystal structures of these adducts allows one to delineate some general trends in the reactivity of these Ru-CORMs with proteins. Indeed, in all cases Ru-CORMs bind these model systems upon detachment of the azole ligand and concomitant coordination to a protein His or Asp residue. Apparently the three Ru-CORMs progressively dissociate losing azoles, chlorides, and one or two CO molecules. Data were compared with those reported in the literature for adducts of the same proteins with other Ru-CORMs and with in-solution data previously obtained on the same systems. These results are potentially useful for a better understanding of the chemistry, potential toxicity and mechanism of actions of these interesting Ru-CORMs and are helpful in defining the molecular mechanisms of CO release.

摘要

fac-[Ru(CO)Cl(N-咪唑)](RuIM)、fac-[Ru(CO)Cl(N-甲基咪唑)](RuMIM)和 fac-[Ru(CO)Cl(N-甲基苯并咪唑)](RuMBI)是三种基于钌的一氧化碳释放分子(Ru-CORM),对卵巢和结肠癌细胞系具有细胞毒性。通过 X 射线晶体学提供了 RuIM 和 RuMIM 与鸡卵清溶菌酶以及三种 Ru-CORM 与牛胰腺核糖核酸酶反应形成的加合物的详细结构信息。对这些加合物的七个晶体结构的比较分析可以描绘出这些 Ru-CORM 与蛋白质反应的一些一般趋势。事实上,在所有情况下,Ru-CORM 都在脱附唑配体并与蛋白质 His 或 Asp 残基配位后结合这些模型系统。显然,三种 Ru-CORM 逐渐解离,失去唑、氯和一个或两个 CO 分子。数据与文献中相同蛋白质与其他 Ru-CORMs 的加合物以及以前在相同体系中获得的溶液数据进行了比较。这些结果对于更好地理解这些有趣的 Ru-CORM 的化学、潜在毒性和作用机制具有潜在的用途,并有助于定义 CO 释放的分子机制。

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