Characterization of the Interaction of Nerve Agent Mimics with Selected Synthetic Receptors

Carolina Braga Barbosa, Patrick Gass, Daniel J. Hamsch, Stefan Kubik
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引用次数: 1

Abstract

Qualitative NMR spectroscopic and quantitative calorimetric binding studies were performed to characterize the interaction of nontoxic mimics of the V-type nerve agent VX and the Novichok nerve agent A-234 with a series of receptors in 100 mM aqueous phosphate buffer at pH 7.4 and 37 °C. These investigations provided information about the preferred geometry with which the nerve agent mimics are included into the receptor cavities and about the stability of the complexes formed. According to the results, the positively charged VX mimic prefers to bind to cation receptors such as sulfonated calixarenes and an acyclic cucurbituril but does not noticeably interact with cyclodextrins. While binding to the acyclic cucurbituril is stronger than that to calixarenes, the mode of inclusion into the sulfonatocalix[4]arene cavity is better suited for the development of scavengers that bind and detoxify V-type nerve agents. The neutral Novichok mimic, on the other hand, only interacts with the acyclic cucurbituril with a strength required for scavenger development. These binding studies thus provided guidelines for the further development of nerve agent scavengers.

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神经毒剂模拟物与选定的合成受体相互作用的表征
定性核磁共振波谱和定量量热结合研究表征了v型神经毒剂VX和诺维乔克神经毒剂a -234的无毒模拟物与一系列受体在pH 7.4和37°C的100 mM磷酸水缓冲液中的相互作用。这些研究提供了有关神经毒剂模拟物进入受体腔的首选几何形状以及形成的复合物的稳定性的信息。结果表明,带正电荷的VX模拟物倾向于与磺化杯芳烃和无环葫芦脲等阳离子受体结合,但与环糊精没有明显的相互作用。虽然与无环葫芦脲的结合强于与杯芳烃的结合,但包裹入磺环环芳烃腔的方式更适合于开发结合和解毒v型神经毒剂的清除剂。另一方面,中性的诺维乔克模拟物仅与无环葫芦脲相互作用,其强度要求清道夫发展。这些结合研究为神经毒剂清除剂的进一步开发提供了指导。
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CiteScore
3.70
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0.00%
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0
审稿时长
12 weeks
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