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利用表面增强拉曼光谱鉴定新出现的流感病毒。

Identification of Newly Emerging Influenza Viruses by Surface-Enhanced Raman Spectroscopy.

机构信息

Department of Bio-convergence Engineering, Korea University , Seoul, 136-713, Korea.

Department of Medical & Pharmaceutical Sciences, Sookmyung Women's University , Seoul, 140-742, Korea.

出版信息

Anal Chem. 2015 Dec 1;87(23):11652-9. doi: 10.1021/acs.analchem.5b02661. Epub 2015 Nov 16.

Abstract

In this work, we demonstrate in situ virus identification based on surface-enhanced Raman scattering (SERS). We hypothesized that newly emerging influenza viruses possess surface proteins and lipids that can generate distinctive Raman signals. To test this hypothesis, SERS signals were measured from the surface of a noninfluenza virus, two different influenza viruses, and a genetically shuffled influenza virus. To ensure the safety for experimenters we constructed nonreplicating pseudotyped viruses that display main influenza virus surface components. Pseudotype with influenza virus components produced enhanced Raman peaks, on gold nanoparticles, that are easily distinguishable from those of pseudotype with a noninfluenza virus component, vesicular stomatitis virus G protein (VSVG). Furthermore, virus with the surface components of a newly emerging influenza strain, A/California/04/2009 (H1N1), generated Raman peaks different from those of viruses with components of the conventional laboratory-adapted influenza strain, A/WSN/33 (H1N1). Interestingly, the virus simultaneously displaying surface components of both influenza strains, a model mutant with genome reassortment, also produced a Raman signal pattern that is clearly distinguishable from those of each strain. This work highlights that SERS can provide a powerful label-free strategy to quickly identify newly emerging and potentially fatal influenza viruses.

摘要

在这项工作中,我们展示了基于表面增强拉曼散射(SERS)的原位病毒识别。我们假设新出现的流感病毒具有可以产生独特拉曼信号的表面蛋白和脂质。为了验证这一假设,我们测量了非流感病毒、两种不同流感病毒和基因改组流感病毒表面的 SERS 信号。为了确保实验人员的安全,我们构建了不复制的假型病毒,这些病毒展示了主要的流感病毒表面成分。具有流感病毒成分的假型病毒在金纳米粒子上产生了增强的拉曼峰,这些峰很容易与具有非流感病毒成分(水疱性口炎病毒 G 蛋白(VSVG))的假型病毒的拉曼峰区分开来。此外,具有新型流感毒株(A/加利福尼亚/04/2009(H1N1))表面成分的病毒产生的拉曼峰与具有常规实验室适应流感毒株(A/WSN/33(H1N1))成分的病毒产生的拉曼峰不同。有趣的是,同时显示两种流感株表面成分的病毒,即具有基因组重配的模型突变体,也产生了一种明显可与每种株区分开来的拉曼信号模式。这项工作强调了 SERS 可以提供一种强大的无标记策略,用于快速识别新出现的和潜在致命的流感病毒。

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