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基于 γ-环糊精与四苯乙烯-甘草酸二钠缀合物主客体识别的荧光“开启”型酶响应超两亲分子的构建。

Fluorescence "Turn-On" Enzyme-Responsive Supra-Amphiphile Fabricated by Host-Guest Recognition between γ-Cyclodextrin and a Tetraphenylethylene-Sodium Glycyrrhetinate Conjugate.

机构信息

Key Laboratory of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, China.

Department of Chemistry, University of Victoria, Victoria, British Columbia V8P 5C2, Canada.

出版信息

Langmuir. 2021 May 18;37(19):6062-6068. doi: 10.1021/acs.langmuir.1c00781. Epub 2021 May 7.

Abstract

A novel fluorescence "turn-on" enzyme-responsive supra-amphiphile is developed based on the host-guest recognition between γ-cyclodextrin (γ-CD) and an amphiphilic tetraphenylethene-sodium glycyrrhetinate conjugate (TPE-SGA). The covalent amphiphile TPE-SGA displayed strong fluorescence in aqueous solution owing to the aggregation-induced emission. Upon addition of γ-CD, the fluorescence of TPE-SGA was effectively turned off due to the host-guest recognition with γ-CD prohibiting the aggregation of TPE-SGA in aqueous solution. The as-formed nonfluorescent supra-amphiphile (TPE-SGA/γ-CD) inherited the α-amylase-responsive property of γ-CD. In the presence of α-amylase, the fluorescence of the supra-amphiphile was gradually turned on owing to the hydrolysis of γ-CD, and the fluorescence intensity linearly correlated to the activity of α-amylase. This study enriches the field of supra-amphiphile on the basis of cyclodextrin-based host-guest chemistry and provides a novel strategy to construct fluorescence turn-on functioned self-assemblies. It is anticipated that the fluorescence turn-on supra-amphiphile has potential applications in biological analysis and diagnosis of pancreatic diseases.

摘要

一种基于γ-环糊精(γ-CD)与两亲性四苯乙烯-甘草次酸钠轭合物(TPE-SGA)之间主客体识别的新型荧光“开启”酶响应超两亲分子被开发出来。由于聚集诱导发射,共价两亲分子 TPE-SGA 在水溶液中显示出强荧光。当加入γ-CD 时,由于主客体识别,TPE-SGA 的荧光被有效关闭,阻止了 TPE-SGA 在水溶液中的聚集。所形成的非荧光超两亲分子(TPE-SGA/γ-CD)继承了 γ-CD 的α-淀粉酶响应特性。在α-淀粉酶存在下,由于γ-CD 的水解,超两亲分子的荧光逐渐开启,荧光强度与α-淀粉酶的活性呈线性相关。本研究丰富了基于环糊精主体客体化学的超两亲分子领域,并提供了一种构建荧光开启功能自组装体的新策略。预计荧光开启超两亲分子在胰腺疾病的生物分析和诊断中有潜在的应用。

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