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Evaluating Quantum Dot Performance in Homogeneous FRET Immunoassays for Prostate Specific Antigen

机译:在前列腺特异性抗原的均相FRET免疫测定中评估量子点性能

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摘要

The integration of semiconductor quantum dots (QDs) into homogeneous Förster resonance energy transfer (FRET) immunoassay kits for clinical diagnostics can provide significant advantages concerning multiplexing and sensitivity. Here we present a facile and functional QD-antibody conjugation method using three commercially available QDs with different photoluminescence (PL) maxima (605 nm, 655 nm, and 705 nm). The QD-antibody conjugates were successfully applied for FRET immunoassays against prostate specific antigen (PSA) in 50 µL serum samples using Lumi4-Tb (Tb) antibody conjugates as FRET donors and time-gated PL detection on a KRYPTOR clinical plate reader. Förster distance and Tb donor background PL were directly related to the analytical sensitivity for PSA, which resulted in the lowest limits of detection for Tb-QD705 (2 ng/mL), followed by Tb-QD655 (4 ng/mL), and Tb-QD605 (23 ng/mL). Duplexed PSA detection using the Tb-QD655 and Tb-QD705 FRET-pairs demonstrated the multiplexing ability of our immunoassays. Our results show that FRET based on QD acceptors is suitable for multiplexed and sensitive biomarker detection in clinical diagnostics.
机译:将半导体量子点(QD)集成到用于临床诊断的均质Förster共振能量转移(FRET)免疫测定试剂盒中,可以提供有关多路复用和灵敏度的显着优势。在这里,我们提出了一种简便且功能强大的QD抗体偶联方法,该方法使用了三个具有不同最大光致发光(PL)(605 nm,655 nm和705 nm)的市售QD。使用Lumi4-Tb(Tb)抗体结合物作为FRET供体,并在KRYPTOR临床读板器上进行时间门控PL检测,QD抗体结合物已成功应用于50 µL血清样品中针对前列腺特异性抗原(PSA)的FRET免疫测定。 Förster距离和Tb供体背景PL与PSA的分析灵敏度直接相关,这导致Tb-QD705(2 ng / mL),Tb-QD655(4 ng / mL)和Tb的最低检测限-QD605(23 ng / mL)。使用Tb-QD655和Tb-QD705 FRET对进行双链PSA检测证明了我们免疫测定的多重能力。我们的结果表明,基于QD受体的FRET适用于临床诊断中的多重和敏感生物标志物检测。

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