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荧光酞菁组装可区分不同类型氨基酸和糖的手性异构体。

Fluorescent Phthalocyanine Assembly Distinguishes Chiral Isomers of Different Types of Amino Acids and Sugars.

机构信息

Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry, University of Science and Technology Beijing , Beijing 100083, P.R. China.

出版信息

Langmuir. 2017 Jul 25;33(29):7239-7247. doi: 10.1021/acs.langmuir.7b01602. Epub 2017 Jul 12.

Abstract

The functions of some natural supramolecular architectures, such as ribosomes, are dependent on the recognition of different types of chiral biomolecules. However, the recognition of different types of chiral molecules (multiobject chiral recognition), such as amino acids and sugars, by independent and identically artificial supramolecular assembly, was rarely achieved. In this article, simple amphiphilic achiral phthalocyanine was found to form supramolecular chiral assemblies with charged water-soluble polymers upon host-guest interactions at the air/water interface. Among these systems, one identical phthalocyanine/poly(l-lysine) assembly not only can distinguish enantiomers of different amino acids but also can recognize several epimers of monose. The chiral recognitions were achieved by comparing either the steady-state fluorescence intensity or fluorescence quenching rate of phthalocyanine/poly(l-lysine) assemblies, before and after interaction with different small chiral molecules. It was demonstrated that the interactions between poly(l-lysine) and different small chiral molecules could change the aggregation of phthalocyanines. And the sensitivity of fluorescence and the excellent multiobject chiral recognition properties of the phthalocyanine/poly(l-lysine) assembly are dependent on the subtle molecular packing mode and the cooperation of different noncovalent interactions.

摘要

一些天然超分子结构的功能,如核糖体,依赖于对不同类型手性生物分子的识别。然而,独立且相同的人工超分子组装对不同类型手性分子(多对象手性识别),如氨基酸和糖的识别,很少被实现。在本文中,我们发现简单的两亲性非手性酞菁在空气/水界面通过主客体相互作用与带电水溶性聚合物形成超分子手性组装体。在这些体系中,一个相同的酞菁/聚(L-赖氨酸)组装体不仅可以区分不同氨基酸的对映体,还可以识别几种单糖的差向异构体。通过比较与不同小的手性分子相互作用前后酞菁/聚(L-赖氨酸)组装体的稳态荧光强度或荧光猝灭率,实现了手性识别。结果表明,聚(L-赖氨酸)与不同小的手性分子之间的相互作用可以改变酞菁的聚集。并且酞菁/聚(L-赖氨酸)组装体的荧光灵敏度和优异的多对象手性识别性能取决于微妙的分子堆积方式和不同非共价相互作用的协同作用。

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