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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Quantum Dot-Based Multidonor Concentric FRET System and Its Application to Biosensing Using an Excitation Ratio
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Quantum Dot-Based Multidonor Concentric FRET System and Its Application to Biosensing Using an Excitation Ratio

机译:基于量子点的多供体同心FRET系统及其在基于激发比的生物传感中的应用

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摘要

A plethora of semiconductor quantum dot (QD)-based probes that rely on Fo?rster resonance energy transfer (FRET) have been developed for the optical detection of a wide array of biological targets. To date, the vast majority of these probes have utilized one-step energy transfer between individual donor?acceptor pairs. Here, we report a new multidonor concentric FRET configuration that comprised two fluorescent dyes assembled around a central CdSeS/ZnS QD through peptide linkers. One of these dyes, either Alexa Fluor 555 (A555) or Alexa Fluor 647 (A647), served as an acceptor for both the central QD and the other coassembled dye, Alexa Fluor 488 (A488). The unresolved emission between the A488 and the QD precluded a standard analysis of FRET efficiency from quenching of donor emission intensity or decay time, instead necessitating an analysis of the two energy transfer pathways from deconvolved excitation spectra. When A647 was the terminal acceptor, both the QD-to-A647 and A488-to-A647 energy transfer pathways could be interrogated with blue light, but only the former could be interrogated with violet light. The different degrees of A647 sensitization between these two excitation wavelengths was a predictable function of the above energy transfer efficiencies and dye stoichiometry, and was exploited for quantitative bioanalysis through an excitation ratio, which is in contrast to the conventional use of an emission ratio with FRETbased probes. Detection of the activity of nanomolar concentrations of trypsin, a model protease that hydrolyzed the A488- labeled peptide linker, was demonstrated using both a fluorescence plate reader and a low-cost, compact device that used two low-power light-emitting diodes (LEDs) as excitation sources and a silicon photodiode to detect A647 emission. This multidonor concentric FRET configuration represents a new modality for ratiometric biosensing with QDs and is potentially useful for portable in vitro diagnostics.
机译:已经开发了许多基于菲斯特共振能量转移(FRET)的基于半导体量子点(QD)的探针,用于光学检测各种生物靶标。迄今为止,这些探针中的绝大部分已经利用了单个供体-受体对之间的一步式能量转移。在这里,我们报告了一种新的多供体同心FRET构型,该构型包括通过肽接头在中央CdSeS / ZnS QD周围组装的两种荧光染料。这些染料之一,即Alexa Fluor 555(A555)或Alexa Fluor 647(A647),均用作中央QD和另一种共组装染料Alexa Fluor 488(A488)的受体。在A488和QD之间的未解决的发射排除了对FRET效率进行标准分析的必要性,因为该分析无法抑制供体发射强度或衰减时间,因此必须从解卷积的激发光谱中分析两个能量转移途径。当A647是末端受体时,QD到A647和A488到A647的能量转移途径都可以用蓝光询问,但是只有前者可以用紫光询问。这两个激发波长之间不同程度的A647敏化程度是上述能量转移效率和染料化学计量的可预测函数,并且已通过激发比被用于定量生物分析,这与传统的使用基于FRET的发射比相反探针。使用荧光板读取器和使用两个低功率发光二极管(LED)的低成本紧凑型设备,证明了纳摩尔浓度的胰蛋白酶(一种水解A488标记的肽接头的模型蛋白酶)的活性检测。 )作为激发源和一个用于检测A647发射的硅光电二极管。这种多供体同心FRET构型代表了具有QD的比例式生物传感的新形式,并可能用于便携式体外诊断。

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