Luminescent Terbium Probe for Time-Resolved FRET and NSET Binding Assays with Quantum Dots and Gold Nanoparticles

IF 3.4 Q2 CHEMISTRY, ANALYTICAL
P. Iyanu Diriwari, N. Connor Payne, Ralph Mazitschek, Thibault Gallavardin, Niko Hildebrandt
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引用次数: 0

Abstract

Time-gated or time-resolved FRET (TR-FRET) assays are important tools in biosensing, bioimaging, drug screening, and molecular diagnostics. Efficient TR-FRET assays require stable lanthanide complexes with high absorption cross sections, high quantum yields, and long photoluminescence lifetimes. Owing to their challenging synthesis, such complexes are relatively rare and new components are of potential interest when developing TR-FRET probes. Here, we evaluate the recently developed Tb complex CoraFluor-1 concerning its analytical performance in terbium-to-quantum dot FRET and terbium-to-gold nanoparticle NSET assays using the prototypical biological recognition system of streptavidin and biotin. Biological binding was quantifiable at sub-picomolar concentrations in small sample volumes, with broad applicability demonstrated across three commercial fluorescence plate readers used for time-resolved, spectrally-resolved, and clinical bioanalysis. Overall, CoraFluor-1 provided excellent analytical performance as both FRET and NSET donor, validating its potential for developing new TR-FRET probes for biosensing and bioimaging.

Abstract Image

发光铽探针的时间分辨FRET和NSET结合测定与量子点和金纳米颗粒
时间门控或时间分辨FRET (TR-FRET)测定是生物传感,生物成像,药物筛选和分子诊断的重要工具。高效的TR-FRET测定需要稳定的镧系配合物,具有高吸收截面,高量子产率和长光致发光寿命。由于它们具有挑战性的合成,这种配合物是相对罕见的,新的成分是开发TR-FRET探针时的潜在兴趣。在这里,我们利用链霉亲和素和生物素的原型生物识别系统,评估了最近开发的Tb配合物CoraFluor-1在铽-量子点FRET和铽-金纳米颗粒NSET分析中的分析性能。生物结合可在小样本量的亚皮摩尔浓度下定量,具有广泛的适用性,通过三种商业荧光板阅读器用于时间分辨,光谱分辨和临床生物分析。总的来说,CoraFluor-1作为FRET和NSET供体都提供了出色的分析性能,验证了其开发用于生物传感和生物成像的新型TR-FRET探针的潜力。
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CiteScore
2.60
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0.00%
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