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电化学发光 CdS 量子点生物传感器用于线性 DNA 分析物不同位置的癌症基因突变检测。

Electrochemiluminescent CdS Quantum Dots Biosensor for Cancer Mutation Detection at Different Positions on Linear DNA Analytes.

机构信息

School of Chemistry, Chemical Engineering, and Life Science, Wuhan University of Technology, Wuhan, Hubei 430070, China.

Shaoxing Institute for Advanced Research, Wuhan University of Technology, Shaoxing, Zhejiang 312300, China.

出版信息

Anal Chem. 2023 Sep 19;95(37):14016-14024. doi: 10.1021/acs.analchem.3c02649. Epub 2023 Sep 8.

Abstract

PCR-based techniques routinely employed for the detection of mutated linear DNA molecules, including circulating tumor DNA (ctDNA), require large nucleotide sections on both sides of the mutation for primer annealing. This means that DNA fragments with a mutation positioned closer to the extremities are unlikely to be detected. Thus, sensors capable of recognizing linear DNA with characteristic mutations closer to the ends would be advantageous over the state-of-the-art approaches. Here, an electrochemiluminescence-resonance energy transfer (ECL-RET) biosensor comprising capped CdS quantum dots and hairpin DNA probes labeled with Au nanoparticles was developed for the detection of epidermal growth factor receptor (EGFR) ctDNA carrying the critical T790M lung cancer mutation. The ECL-RET system detected different DNA molecules including single-stranded 18-nucleotides (nt) and 40-nt as well as double-stranded 100-nt with the single nucleotide polymorphism (SNP) coding for T790M located either in the middle or only 7 nt from one end. For all target DNA, the sensor's limits of detection (LODs) were in the aM range, with excellent selectivity. It was the case of 100-nt target linear ctDNA fragments with LODs of 8.1 and 3.4 aM when the EGFR T790M SNP was either in the middle or at the end, respectively. These results show that ECL-RET systems can sense mutations in DNA fragments that would remain undetected by standard techniques.

摘要

基于 PCR 的技术常用于检测突变线性 DNA 分子,包括循环肿瘤 DNA(ctDNA),需要在突变两侧有较大的核苷酸序列用于引物退火。这意味着位于突变位置更接近末端的 DNA 片段不太可能被检测到。因此,能够识别特征性突变更接近末端的线性 DNA 的传感器将比现有技术更具优势。在这里,开发了一种包含盖帽 CdS 量子点和带有金纳米粒子标记的发夹 DNA 探针的电化学发光共振能量转移(ECL-RET)生物传感器,用于检测携带关键 T790M 肺癌突变的表皮生长因子受体(EGFR)ctDNA。ECL-RET 系统检测了不同的 DNA 分子,包括单链 18 个核苷酸(nt)和 40-nt 以及双链 100-nt,其中 SNP 编码 T790M 位于中间或仅离一端 7 nt 处。对于所有目标 DNA,传感器的检测限(LOD)在 aM 范围内,具有优异的选择性。对于 100-nt 目标线性 ctDNA 片段,当 EGFR T790M SNP 分别位于中间或末端时,其 LOD 分别为 8.1 和 3.4 aM。这些结果表明,ECL-RET 系统可以检测到标准技术无法检测到的 DNA 片段中的突变。

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