Spectroscopy and Spectral Analysis, Volume. 40, Issue 10, 3021(2020)

Research Progress and Application of Surface-Enhanced Raman Scattering Technique in Nucleic Acid Detection

Hui-yan TIAN1...1,*, Yu LIU1,1, Jiao-qi HUANG1,1, Feng-xin XIE1,1, Guo-rong HUANG1,1, Pu LIAO1,1, Wei-ling FU1,1, and Yang ZHANG11 |Show fewer author(s)
Author Affiliations
  • 1[in Chinese]
  • 11. Department of Clinical Laboratory, The First Affiliated Hospital of the Army Military Medical University, Chongqing 400038, China
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    Figures & Tables(9)
    Principle of SERS(a) Illustration of the collective oscillation of free electrons in metal nanoparticles upon excitation by an electromagnetic wave; (b) Chemical enhancement results from charge transfer resonance between signal molecules and metal nanostructures, which is usually weaker than electromagnetic enhancement
    SERS-based nucleic acid analysis using a label-free SERS approach (left) or SERS tags (right)In label-free SERS, the spectroscopic signal results from analyte adsorption onto the SERS substrate, whereas in SERS tags-based specific recognition assays, the spectroscopic signal results from the reporter molecules on the SERS tags
    Scheme of SERS-based nucleic acid detection based on sandwich structure[18]
    (A) Schematic illustration of the synthetic procedures of Raman dye-coded Au-RNNPs using DNA-modified AuNPs as templates (a) and Ag-HMSs using bacteria as template; (B) Schematic illustration of the multiplex SERS assay for triple-target miRNA detection; (C)SERS spectra of the nanoprobes obtained in the presence of (a) single and (b) multiple miRNA[19]
    Scheme of SERS-based nucleic acid detection based on hairpin structure[18]
    (a) Schematic illustration of the molecular beacons functionalized-SERS sensor for simultaneously measuring multiple miRNAs[24]; (b) Detection scheme of the SERS “inverse Molecular Sentinel” nanoprobes[25]
    Scheme of SERS-based nucleic acid detection based on the signal amplification of hybridization chain reaction[26,27]
    • Table 1. Analysis of the label-free SERS approach and SERS tags-based nucleic acid assays

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      Table 1. Analysis of the label-free SERS approach and SERS tags-based nucleic acid assays

      检测方法优点缺点
      无标记检测(1) 步骤简单, 无需对样品进行处理, 可以避免对生物体的破坏, 最大限度地保持生物体的活性;
      (2)可以充分发挥SERS作为振动光谱具有指纹识别的优势, 得到DNA自身的结构信息。
      (1) 在实际SERS检测中, 由于碱基的拉曼散射截面很小, 导致DNA/RNA的SERS信号很弱, 检测灵敏度较低;
      (2) 不同的DNA/RNA序列具有相同的碱基种类只是碱基排列顺序不同, 因而具有相似的SERS光谱, 很难直接通过SERS信号来确定特定的DNA序列, 需要借助一些数据分析手段。
      标记型检测特异性好, 灵敏度高, 可直接进行定量检测在检测结构及探针的设计上有一定的难度。
    • Table 2. Typical research about SERS used for detection on nucleic acids

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      Table 2. Typical research about SERS used for detection on nucleic acids

      目标核酸SERS检测方法LOD/判别正确率参考文献
      肝癌miRNA标志物(miRNA-21, miRNA-122, miRNA-223)“夹心法”检测: Ag微球偶联DNA捕获链, Au RNNP-44DP/4ATP/DTNB DNA探针10 fmol·L-1[15]
      乙型肝炎病毒DNA“夹心法”检测: Ag nanorice @MGITC @SiO250 amol·L-1[16]
      复合病原体 DNA“夹心法”检测: Au NPS DNA探针, 150 nm 的金纳米棒上构建检测基底10 pmol·L-1[17]
      肺癌miRNA标志物(miRNA 21, miRNA 486, miRNA 375)“信号开—关法”: 发夹探针-ROX/Cy5/FAM, Ag NRs微阵列增强基底miRNA 21/393 amol·L-1, miRNA 486/176 amol·L-1, miRNA 375/144 amol·L-1[20]
      肺癌miRNA标志物(miRNA 21, miRNA 34a)“信号关—开法”: 发夹探针-Cy5/Cy5.5, Ag-coated Au nanostars增强基底成功实现对生物样本中混合miRNA标志物的检测[21]
      miRNA 141“HCR信号放大法”: Au NPS在DNA聚合物上形成“热点”效应0.17 fmol·L-1[22]
      miRNA 21“HCR信号放大法”: Ag NPS在DNA聚合物上形成“热点”效应对单碱基突变及双碱基突变序列的检测信号点分别仅为12.4%和4.6%(定义对靶序列miRNA-21的检测信号点100%)[23]
      miRNA-150“信号开—关法”: 发夹探针-Cy5-Au NPS70.2 amol·L-1[24]
      DNA“热点效应”: 通过ss-DNA的自组装在Au NPS间形成“热点”, 再利用酶切技术进行“热点”消除通过检测拉曼报告分子拉曼信号的变化, 证明该方法可行[25]
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    Hui-yan TIAN, Yu LIU, Jiao-qi HUANG, Feng-xin XIE, Guo-rong HUANG, Pu LIAO, Wei-ling FU, Yang ZHANG. Research Progress and Application of Surface-Enhanced Raman Scattering Technique in Nucleic Acid Detection[J]. Spectroscopy and Spectral Analysis, 2020, 40(10): 3021

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    Paper Information

    Category: Research Articles

    Received: Jul. 17, 2019

    Accepted: --

    Published Online: Jun. 18, 2021

    The Author Email: TIAN Hui-yan (393602704@qq.com)

    DOI:10.3964/j.issn.1000-0593(2020)10-3021-08

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