Enzymatic ablation of bimetallic Au@Ag nanocomposites enabling the smartphone-based colorimetric visualization of S1 nuclease

IF 3.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Ziqing Qiu , Xiaojun Liu , Yanfei Zhang , Shu Zhu , Meiyun Chen , Yujie Zhao , Xingyu Luo
{"title":"Enzymatic ablation of bimetallic Au@Ag nanocomposites enabling the smartphone-based colorimetric visualization of S1 nuclease","authors":"Ziqing Qiu ,&nbsp;Xiaojun Liu ,&nbsp;Yanfei Zhang ,&nbsp;Shu Zhu ,&nbsp;Meiyun Chen ,&nbsp;Yujie Zhao ,&nbsp;Xingyu Luo","doi":"10.1016/j.snb.2025.137487","DOIUrl":null,"url":null,"abstract":"<div><div>S1 nuclease is an important endonuclease involved in multiple biological processes. It is essential to develop suitable detection methods to analyze the S1 nuclease activity for further understanding its biological functions. Although conventional methods for S1 nuclease detection have been well-designed including the gold nanoparticles (AuNPs)-related analytical methods. It still remains challenges in further improving their detection performances. To address these challenges, we report a novel smartphone-based colorimetric sensing method using the bimetallic Au@Ag nanocomposites (Au@Ag NCs) to realize the portable, sensitive, analytical instrument-free, and visual detection of S1 nuclease in real samples. In this method, the bare AuNPs was primarily modified with L1 DNA for supporting the silver (Ag) shell. With the formation of Ag shell, the prepared Au@Ag NCs display the enhanced localized surface plasma resonance (LSPR) effect by producing the characteristic UV–vis absorption peak of Ag (<em>Abs</em><sub>Ag</sub>), while the <em>Abs</em><sub>Au</sub>/<em>Abs</em><sub>Ag</sub> values will be promoted by the enzymatic ablation of Ag shell when L1 DNA was cleaved by S1 nuclease. Thus, Au@Ag NCs allow the colorimetric, sensitive and selective sensing toward S1 nuclease activity with the detection linear range varied from 0.1 to 50 U/mL and the detection limit as low as 0.02 U/mL. Furthermore, the colorimetric signals change also display the obvious color change in Au@Ag NCs and a smartphone-based sensing platform has been constructed to reveal the Red/Green/Blue (RGB) quantification and visual analysis of S1 nuclease in different scenarios. Therefore, this method will hold great potential in realizing the S1 nuclease detection with preferable detection performances.</div></div>","PeriodicalId":425,"journal":{"name":"Sensors and Actuators B: Chemical","volume":"432 ","pages":"Article 137487"},"PeriodicalIF":3.7000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sensors and Actuators B: Chemical","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S092540052500262X","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

S1 nuclease is an important endonuclease involved in multiple biological processes. It is essential to develop suitable detection methods to analyze the S1 nuclease activity for further understanding its biological functions. Although conventional methods for S1 nuclease detection have been well-designed including the gold nanoparticles (AuNPs)-related analytical methods. It still remains challenges in further improving their detection performances. To address these challenges, we report a novel smartphone-based colorimetric sensing method using the bimetallic Au@Ag nanocomposites (Au@Ag NCs) to realize the portable, sensitive, analytical instrument-free, and visual detection of S1 nuclease in real samples. In this method, the bare AuNPs was primarily modified with L1 DNA for supporting the silver (Ag) shell. With the formation of Ag shell, the prepared Au@Ag NCs display the enhanced localized surface plasma resonance (LSPR) effect by producing the characteristic UV–vis absorption peak of Ag (AbsAg), while the AbsAu/AbsAg values will be promoted by the enzymatic ablation of Ag shell when L1 DNA was cleaved by S1 nuclease. Thus, Au@Ag NCs allow the colorimetric, sensitive and selective sensing toward S1 nuclease activity with the detection linear range varied from 0.1 to 50 U/mL and the detection limit as low as 0.02 U/mL. Furthermore, the colorimetric signals change also display the obvious color change in Au@Ag NCs and a smartphone-based sensing platform has been constructed to reveal the Red/Green/Blue (RGB) quantification and visual analysis of S1 nuclease in different scenarios. Therefore, this method will hold great potential in realizing the S1 nuclease detection with preferable detection performances.

Abstract Image

酶消融双金属Au@Ag纳米复合材料,实现基于智能手机的S1核酸酶比色可视化
S1核酸酶是一种重要的核酸内切酶,参与多种生物过程。为了进一步了解S1核酸酶的生物学功能,有必要建立合适的检测方法来分析其活性。虽然传统的S1核酸酶检测方法已经设计得很好,包括金纳米颗粒(AuNPs)相关的分析方法。如何进一步提高它们的检测性能仍然是一个挑战。为了解决这些挑战,我们报告了一种新的基于智能手机的比色传感方法,该方法使用双金属Au@Ag纳米复合材料(Au@Ag NCs)实现了真实样品中S1核酸酶的便携式,灵敏,无分析仪器和视觉检测。在这种方法中,裸AuNPs主要用L1 DNA修饰以支持银(Ag)壳。随着银壳的形成,制备的Au@Ag纳米碳纳米管通过产生银的特征紫外-可见吸收峰(AbsAg)表现出增强的局部表面等离子体共振(LSPR)效应,而当S1核酸酶切割L1 DNA时,Ag壳的酶切会提高AbsAu/AbsAg值。因此,Au@Ag NCs可对S1核酸酶活性进行比色、灵敏和选择性检测,检测线性范围为0.1 ~ 50 U/mL,检出限低至0.02 U/mL。此外,比色信号的变化也显示了Au@Ag NCs中明显的颜色变化,并构建了基于智能手机的传感平台,揭示了S1核酸酶在不同场景下的红/绿/蓝(RGB)定量和可视化分析。因此,该方法在实现具有较好检测性能的S1核酸酶检测方面具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Sensors and Actuators B: Chemical
Sensors and Actuators B: Chemical 工程技术-电化学
CiteScore
14.60
自引率
11.90%
发文量
1776
审稿时长
3.2 months
期刊介绍: Sensors & Actuators, B: Chemical is an international journal focused on the research and development of chemical transducers. It covers chemical sensors and biosensors, chemical actuators, and analytical microsystems. The journal is interdisciplinary, aiming to publish original works showcasing substantial advancements beyond the current state of the art in these fields, with practical applicability to solving meaningful analytical problems. Review articles are accepted by invitation from an Editor of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信