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Time-Resolved Analysis of a Highly Sensitive Förster Resonance Energy Transfer Immunoassay Using Terbium Complexes as Donors and Quantum Dots as Acceptors

机译:Ter配合物作为供体和量子点作为受体的高灵敏度福斯特共振能量转移免疫测定的时间分辨分析

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摘要

CdSe/ZnS core/shell quantum dots (QDs) are used as efficient Förster Resonance Energy Transfer (FRET) acceptors in a time-resolved immunoassays with Tb complexes as donors providing a long-lived luminescence decay. A detailed decay time analysis of the FRET process is presented. QD FRET sensitization is evidenced by a more than 1000-fold increase of the QD luminescence decay time reaching ca. 0.5 milliseconds, the same value to which the Tb donor decay time is quenched due to FRET to the QD acceptors. The FRET system has an extremely large Förster radius of approx. 100 Å and more than 70% FRET efficiency with a mean donor-acceptor distance of ca. 84 Å, confirming the applied biotin-streptavidin binding system. Time-resolved measurement allows for suppression of short-lived emission due to background fluorescence and directly excited QDs. By this means a detection limit of 18 attomol QDs within the immunoassay is accomplished, an improvement of more than two orders of magnitude compared to commercial systems.
机译:CdSe / ZnS核/壳量子点(QDs)在具有Tb配合物的时间分辨免疫测定中用作有效的Förster共振能量转移(FRET)受体,作为供体,可提供长寿命的发光衰变。给出了FRET过程的详细衰减时间分析。 QD FRET敏化由QD发光衰减时间达到1000倍以上所证明。 0.5毫秒,由于对QD受体的FRET,Tb供体衰变时间被淬灭到相同的值。 FRET系统的Förster半径非常大。 100Å和超过70%的FRET效率,平均供体-受体距离为。 84Å,证实了所应用的生物素-链霉亲和素结合系统。时间分辨测量可以抑制由于背景荧光和直接激发的QD引起的短时发射。通过这种方法,可以实现免疫测定中18个attomol QD的检测极限,与商用系统相比,提高了两个数量级以上。

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