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Energy Transfer-Based Multiplexed Assay of Proteases by Using Gold Nanoparticle and Quantum Dot Conjugates on a Surface

机译:在表面上使用金纳米粒子和量子点结合物的基于能量转移的蛋白酶蛋白酶多路复用测定

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摘要

Rapid and sensitive assay of proteases and their inhibition in a high-throughput manner is of great significance in the diagnostic and pharmaceutical fields. We developed a multiplexed assay system of proteases and their inhibition by measuring the energy transfer between quantum dots (QDs) and gold nanoparticles (AuNPs) on a glass slide. In this system, while the photoluminescence (PL) of donor QDs immobilized on a surface was quenched due to the presence of AuNPs (energy acceptor) in close proximity, the protease activity caused modulation in the efficiency of the energy transfer between the acceptor and donor, thus enabling the protease assay. In comparison to the QD-dye system, the conjugate of the QD-AuNP gave rise to higher energy transfer efficiency, resulting in quantitative assay of proteases with more sensitivity. When matrix metalloproteinase, caspase, and thrombin were tested, a multiplexed assay was successfully achieved since the AuNP could be used as a common energy acceptor in conjunction with QDs having different colors. Our system is anticipated to find applications in the diagnosis of protease-related diseases and screening of potential drugs with high sensitivity in a high-throughput way.
机译:蛋白酶的快速灵敏测定及其以高通量方式的抑制在诊断和制药领域具有重要意义。我们通过测量载玻片上量子点(QD)和金纳米颗粒(AuNPs)之间的能量转移,开发了一种蛋白酶及其抑制作用的多重测定系统。在该系统中,固定在表面的供体QD的光致发光(PL)由于紧邻的AuNPs(能量受体)的存在而被淬灭,但蛋白酶的活性导致受体与供体之间能量转移效率的调节,因此可以进行蛋白酶测定。与QD-染料系统相比,QD-AuNP的共轭物具有更高的能量转移效率,从而可以更灵敏地定量分析蛋白酶。当测试基质金属蛋白酶,胱天蛋白酶和凝血酶时,由于AuNP可以与具有不同颜色的QD一起用作常见的能量受体,因此成功实现了多重测定。我们的系统有望在蛋白酶相关疾病的诊断和以高通量方式高灵敏度筛选潜在药物中找到应用。

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