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核基因组和线粒体基因组中的平行 G-四链体 DNA 结构触发了基于氟硼的无荧光纳米聚集染料的发射增强。

Parallel G-Quadruplex DNA Structures from Nuclear and Mitochondrial Genomes Trigger Emission Enhancement in a Nonfluorescent Nano-aggregated Fluorine-Boron-Based Dye.

机构信息

Department of Medical Biochemistry and Biophysics, Umeå University, 90187 Umeå, Sweden.

Department of Chemistry, Umeå University, 90187 Umeå, Sweden.

出版信息

J Phys Chem Lett. 2023 Feb 23;14(7):1862-1869. doi: 10.1021/acs.jpclett.2c03301. Epub 2023 Feb 13.

DOI:10.1021/acs.jpclett.2c03301
PMID:36779779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9940295/
Abstract

Molecular self-assembly is a powerful tool for the development of functional nanostructures with adaptive optical properties. However, in aqueous solution, the hydrophobic effects in the monomeric units often afford supramolecular architectures with typical side-by-side π-stacking arrangement with compromised emissive properties. Here, we report on the role of parallel DNA guanine quadruplexes (G4s) as supramolecular disaggregating-capture systems capable of coordinating a zwitterionic fluorine-boron-based dye and promoting activation of its fluorescence signal. The dye's high binding affinity for parallel G4s compared to nonparallel topologies leads to a selective disassembly of the dye's supramolecular state upon contact with parallel G4s. This results in a strong and selective disaggregation-induced emission that signals the presence of parallel G4s observable by the naked eye and inside cells. The molecular recognition strategy reported here will be useful for a multitude of affinity-based applications with potential in sensing and imaging systems.

摘要

分子自组装是一种强大的工具,可用于开发具有自适应光学特性的功能纳米结构。然而,在水溶液中,单体单元中的疏水效应往往会提供具有典型并排 π-堆积排列的超分子结构,从而损害发光性能。在这里,我们报告了平行 DNA 鸟嘌呤四链体 (G4) 作为超分子解聚-捕获系统的作用,该系统能够协调两性离子氟硼基染料并促进其荧光信号的激活。与非平行拓扑结构相比,染料对平行 G4 的高结合亲和力导致与平行 G4 接触时,染料的超分子状态选择性解组装。这导致强烈且选择性的解组装诱导发射,可通过肉眼和细胞内观察到平行 G4 的存在。这里报道的分子识别策略将有助于多种基于亲和力的应用,在传感和成像系统中具有潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/b0322cdf44ad/jz2c03301_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/f5d6ae432348/jz2c03301_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/bb9b6daf5c4b/jz2c03301_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/4dcc5efb6057/jz2c03301_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/89ee76cf320e/jz2c03301_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/ec45b0cc7d53/jz2c03301_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/b0322cdf44ad/jz2c03301_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/f5d6ae432348/jz2c03301_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/bb9b6daf5c4b/jz2c03301_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/4dcc5efb6057/jz2c03301_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/89ee76cf320e/jz2c03301_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/ec45b0cc7d53/jz2c03301_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee6/9940295/b0322cdf44ad/jz2c03301_0005.jpg

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