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自组装的银(I)-碱基纳米纤维中的类 DNA 光物理性质

DNA-like Photophysics in Self-Assembled Silver(I)-Nucleobase Nanofibers.

机构信息

Department of Chemistry and Biochemistry , The Ohio State University , 100 West 18th Avenue , Columbus , Ohio 43210 , United States.

出版信息

J Phys Chem B. 2019 Jul 18;123(28):5985-5994. doi: 10.1021/acs.jpcb.9b00660. Epub 2019 Jul 8.

Abstract

Supramolecular assemblies form when silver nitrate is added to an aqueous solution of adenine (Ade) or 2-aminopurine (2AP) in a 2:1 mole ratio. Atomic force microscopy images reveal nanofibers that are ∼30 nm in diameter and micrometers in length in the dried film formed from a room-temperature solution. Femtosecond broadband transient absorption spectroscopy was used to investigate the dynamics of excited states formed by UV excitation of the nanofibers in room-temperature aqueous solutions in an effort to learn how nonradiative decay pathways of the uncomplexed nucleobases are altered in the silver-ion-mediated assemblies. The changes in the spectroscopy and dynamics of Ade and 2AP upon forming nanofibers with silver ions closely parallel the ones seen when these bases are organized into DNA strands. The similarities strongly suggest that these structures feature extensive π-π stacking interactions between nucleobases. The results show that time-resolved spectroscopy combined with growing understanding of the photophysics of DNA strands can deliver new insights into the properties of metal-nucleobase nanoassemblies.

摘要

当硝酸银以 2:1 的摩尔比添加到腺嘌呤(Ade)或 2-氨基嘌呤(2AP)的水溶液中时,会形成超分子组装体。原子力显微镜图像显示,在室温下形成的干燥薄膜中,纳米纤维的直径约为 30nm,长度为数微米。飞秒宽带瞬态吸收光谱用于研究在室温水溶液中通过纳米纤维的 UV 激发形成的激发态的动力学,以了解未配位的核碱基的非辐射衰减途径在银离子介导的组装体中如何被改变。腺嘌呤和 2AP 在与银离子形成纳米纤维时,其光谱和动力学的变化与这些碱基在 DNA 链中组织时的变化非常相似。这些相似之处强烈表明这些结构具有核碱基之间广泛的π-π 堆积相互作用。结果表明,时间分辨光谱学结合对 DNA 链光物理的不断深入理解,可以为金属-核碱基纳米组装体的性质提供新的见解。

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