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基于长波长染料Cy5™发光衰减时间的葡萄糖光学检测法。

Optical assay for glucose based on the luminescnence decay time of the long wavelength dye Cy5™.

作者信息

Tolosa Leah, Malak Henryk, Raob Govind, Lakowicz Joseph R

机构信息

Center for Fluorescence Spectroscopy, Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, 725 West Lombard Street, Baltimore, MD 21201, USA.

Medical Biotechnology Center and Department of Chemical and Biochemical Engineering, 725 West Lombard Street, Baltimore, MD 21201, USA.

出版信息

Sens Actuators B Chem. 1997 Dec;45(2):93-99. doi: 10.1016/S0925-4005(97)00275-X. Epub 1998 Mar 26.

Abstract

An optical assay for glucose is described based on the luminescence decay time of a long wavelength dye (Cy5) which can be excited with currently available red laser diodes. Concanavalin A was covalently labeled with Cy5 which served as the donor in an assay based on fluorescence resonance energy transfer (FRET). The acceptor was Malachite Green which was covalently linked to insulin which served as a carrier protein. To provide binding affinity for ConA Malachite Green insulin was also covalently labeled with maltose (MIMG). Binding of Cy5ConA to MIMG resulted in a decreased intensity and decay time of Cy5 as observed by time-correlated single photon counting. Glucose was detected by competitive displacement of MIMG from Cy5ConA, resulting in increased intensity and decay time. This glucose assay has several features which can result in practical real world assays for glucose. The long absorption wavelength of Cy5 allows excitation with red laser diodes, which can be readily pulsed or amplitude-modulated for time-domain or frequency-domain decay time measurements. Additionally, decay times can be measured through skin using long wavelength excitation and emission, suggesting the possibility of an implanted glucose sensor. And finally, the assay affinity and reversibility can in principle be adjusted by controlling the extent and type of sugar labeling of the carrier protein.

摘要

本文描述了一种基于长波长染料(Cy5)发光衰减时间的葡萄糖光学检测方法,该染料可用现有的红色激光二极管激发。伴刀豆球蛋白A(Concanavalin A)用Cy5进行共价标记,在基于荧光共振能量转移(FRET)的检测中作为供体。受体是孔雀石绿,它与作为载体蛋白的胰岛素共价连接。为了提供对伴刀豆球蛋白A的结合亲和力,孔雀石绿胰岛素也用麦芽糖进行了共价标记(MIMG)。通过时间相关单光子计数观察到,Cy5ConA与MIMG的结合导致Cy5的强度和衰减时间降低。通过将MIMG从Cy5ConA上竞争性置换来检测葡萄糖,这会导致强度和衰减时间增加。这种葡萄糖检测方法具有几个特点,可用于实际的葡萄糖检测。Cy5的长吸收波长允许用红色激光二极管激发,这种二极管可方便地进行脉冲或幅度调制,用于时域或频域衰减时间测量。此外,可使用长波长激发和发射通过皮肤测量衰减时间,这表明植入式葡萄糖传感器具有可能性。最后,检测亲和力和可逆性原则上可通过控制载体蛋白糖标记的程度和类型来调节。

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