Sensitive detection of point mutation using exponential strand displacement amplification-based surface enhanced Raman spectroscopy

• Published in: Biosensors & bioelectronics Vol. 65; pp. 191 - 197
• Main Authors: Huang, Si-qiang, Hu, Juan, Zhu, Guichi, Zhang, Chun-yang
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 15.03.2015
• Subjects: Amplification; Biosensing Techniques - methods; Biosensors; Diagnosis; Displacement; Exponential strand displacement amplification; Genes, ras; HEK293 Cells; Humans; K-ras gene; Mutations; Nucleic Acid Amplification Techniques - methods; Point Mutation; Raman spectroscopy; Recognition; Spectrum Analysis, Raman - methods; Strands; Surface enhanced Raman spectroscopy; Exponential strand displacement amplification; K-ras gene; Point mutation; Surface enhanced Raman spectroscopy
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2014.10.035

Accurate identification of point mutation is particularly imperative in the field of biomedical research and clinical diagnosis. Here, we develop a sensitive and specific method for point mutation assay using exponential strand displacement amplification (SDA)-based surface enhanced Raman spectroscopy (SERS). In this method, a discriminating probe and a hairpin probe are designed to specifically recognize the sequence of human K-ras gene. In the presence of K-ras mutant target (C→T), the 3′-terminal of discriminating probe and the 5′-terminal of hairpin probe can be ligated to form a SDA template. Subsequently, the 3′-terminal of hairpin probe can function as a primer to initiate the SDA reaction, producing a large amount of triggers. The resultant triggers can further hybridize with the discriminating probes to initiate new rounds of SDA reaction, leading to an exponential amplification reaction. With the addition of capture probe-modified gold nanoparticles (AuNPs) and the Rox-labeled reporter probes, the amplified triggers can be assembled on the surface of AuNPs through the formation of sandwich hybrids of capture probe–trigger–reporter probe, generating a strong Raman signal. While in the presence of K-ras wild-type target (C), neither ligation nor SDA reaction can be initiated and no Raman signal is observed. The proposed method exhibits high sensitivity with a detection limit of 1.4pM and can accurately discriminate as low as 1% variant frequency from the mixture of mutant target and wild-type target. Importantly, this method can be further applied to analyze the mutant target in the spiked HEK293T cell lysate, holding great potential for genetic analysis and disease prognosis. •We develop a new method for point mutation assay using exponential strand displacement amplification (SDA)-based SERS.•This method exhibits high sensitivity and can accurately discriminate as low as 1% variant frequency.•This method can be further applied to analyze the mutant target in the spiked HEK293T cell lysate.