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双功能封端剂介导的银纳米三角形向银纳米簇的转变用于双模式生物传感

Dual-Functional Capping Agent-Mediated Transformation of Silver Nanotriangles to Silver Nanoclusters for Dual-Mode Biosensing.

作者信息

He Meng-Qi, Ai Yongjian, Hu Wanting, Jia Xiaomeng, Wu Lei, Ding Mingyu, Liang Qionglin

机构信息

MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Laboratory of Flexible Electronics Technology, Center for Synthetic and Systems Biology, Tsinghua University-Peking University Joint Centre for Life Sciences, Tsinghua University, Beijing 100084, P. R. China.

出版信息

Anal Chem. 2023 Apr 11;95(14):6130-6137. doi: 10.1021/acs.analchem.3c00426. Epub 2023 Mar 31.

Abstract

The localized surface plasmon resonance (LSPR) property, depending on the structure (morphology and assembly) of nanoparticles, is very sensitive to the environmental fluctuation. Retaining the colorimetric effect derived from the LSPR property while introducing new optical properties (such as fluorescence) that provide supplementary information is an effective means to improve the controllability in structures and reproducibility in optical properties. DNA as a green and low-cost etching agent has been demonstrated to effectively control the morphology and optical properties (the blue shift of the LSPR peak) of the plasmonic nanoparticles. Herein, taking silver nanotriangles (AgNTs) as a proof of concept, we report a novel strategy to induce precisely tunable LSPR and fluorescence-composited dual-mode signals by using mono-DNA first as an etching agent for etching the morphology of AgNTs and later as a template for synthesizing fluorescent silver nanoclusters (AgNCs). In addition, common templates for synthesizing AgNCs, such as l-glutathione and bovine serum albumin, were demonstrated to have the capability to serve as etching agents. More importantly, these biomolecules as dual-functional capping agents (etching agents and templates) follow the size-dependent rule: as the size of the thiolated biomolecule increases, the blue shift of the LSPR peak increases; at the same time, the fluorescence intensity increases. The enzyme that can change the molecular weight (size) of the biomolecular substrates (DNA, peptides, and proteins) through an enzymatic cleavage reaction was explored to regulate the LSPR and fluorescent properties of the resulting nanoparticles (by etching of AgNTs and synthesis of AgNCs), achieving excellent performance in detection of cancer-related proteases. This study can be expanded to other biopolymers to impact both fundamental nanoscience and applications and provide powerful new tools for bioanalytical biosensors and nanomedicine.

摘要

局域表面等离子体共振(LSPR)特性取决于纳米粒子的结构(形态和组装),对环境波动非常敏感。在引入提供补充信息的新光学特性(如荧光)的同时,保留源自LSPR特性的比色效应,是提高结构可控性和光学特性再现性的有效手段。DNA作为一种绿色且低成本的蚀刻剂,已被证明能有效控制等离子体纳米粒子的形态和光学特性(LSPR峰的蓝移)。在此,以银纳米三角形(AgNTs)作为概念验证,我们报告了一种新颖的策略,即首先使用单链DNA作为蚀刻剂来蚀刻AgNTs的形态,随后将其作为合成荧光银纳米团簇(AgNCs)的模板,从而诱导出精确可调的LSPR和荧光复合双模式信号。此外,已证明用于合成AgNCs的常见模板,如L-谷胱甘肽和牛血清白蛋白,有能力作为蚀刻剂。更重要的是,这些作为双功能封端剂(蚀刻剂和模板)的生物分子遵循尺寸依赖规则:随着硫醇化生物分子尺寸的增加,LSPR峰的蓝移增加;同时,荧光强度增加。通过酶促裂解反应改变生物分子底物(DNA、肽和蛋白质)分子量(尺寸)的酶被用于调节所得纳米粒子的LSPR和荧光特性(通过蚀刻AgNTs和合成AgNCs),在癌症相关蛋白酶的检测中取得了优异的性能。这项研究可扩展到其他生物聚合物,以影响基础纳米科学和应用,并为生物分析生物传感器和纳米医学提供强大的新工具。

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