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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Gold nanoprobe-based method for sensing activated leukocyte cell adhesion molecule (ALCAM) gene expression, as a breast cancer biomarker
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Gold nanoprobe-based method for sensing activated leukocyte cell adhesion molecule (ALCAM) gene expression, as a breast cancer biomarker

机译:基于金纳米探针的检测活化白细胞粘附分子(ALCAM)基因表达的方法,作为乳腺癌的生物标志物

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摘要

Abstract In breast cancer, a proper biomarker for the assessment of metastasis and poor prognosis is the RNA of activated leukocyte cell adhesion molecule (ALCAM) gene, which is expressed at high levels in breast tumor. We applied DNA-functionalized gold nanoparticles as the target-specific probes, for detecting specific sequences of DNA or RNA. At high MgCL2 concentrations, nanoprobes aggregate in the absence of the complementary DNA sequence and alteration in the solution color is detectable by evaluating the localized surface plasmon resonance (LSPR). But in the presence of complementary DNA, nanoprobes hybridize to the complementary sequence; therefore, no aggregation takes place, and no color change is observed. We designed a gold nanoprobe-based method that promptly detects the ALCAM gene expression in a low reaction volume with high sensitivity and specificity. This method is simple, fast, selective, and quantitative and can be done with small concentrations of the target (fmol/μL). Limit of detection of the method corresponded to 300?fmol/μL of synthetic ALCAM target.
机译:摘要乳腺癌中活化白细胞粘附分子(ALCAM)基因的RNA在乳腺癌中高表达,是评估转移和预后不良的合适生物标志物。我们将DNA功能化的金纳米颗粒用作目标特异性探针,以检测DNA或RNA的特定序列。在高MgCL2浓度下,纳米探针在不存在互补DNA序列的情况下聚集,并且可以通过评估局部表面等离振子共振(LSPR)来检测溶液颜色的变化。但是在存在互补DNA的情况下,纳米探针会与互补序列杂交。因此,没有发生聚集,也没有观察到颜色变化。我们设计了一种基于金纳米探针的方法,该方法可在低反应量下以高灵敏度和特异性迅速检测ALCAM基因的表达。该方法简单,快速,选择性和定量,可以用低浓度的目标物(fmol /μL)完成。该方法的检出限相当于合成ALCAM靶标的300 µfmol /μL。

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