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A Fluorogenic Probe for Cell Surface Phosphatidylserine Using an Intramolecular Indicator Displacement Sensing Mechanism

机译:使用分子内指示剂位移传感机制的细胞表面磷脂酰丝氨酸的荧光探针

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摘要

The detection of externalized phosphatidylserine (PS) on the cell surface is commonly used to distinguish between living, apoptotic, and necrotic cells. The tools of choice for many researchers to study apoptosis are annexin V-fluorophore conjugates. However, the use of this 35 kDa protein is associated with several drawbacks, including temperature sensitivity, Ca2+ dependence, and slow binding kinetics. Herein, a fluorogenic probe for cell surface PS, P-IID, is described, which operates by an intramolecular indicator displacement (IID) mechanism. An intramolecularly bound coumarin indicator is released in the presence of cell surface PS, leading to a fluorescence "turn-on" response. P-IID demonstrates superior performance when compared to annexin V, for both fluorescence imaging and flow cytometry. This allows P-IID to be used in time-lapse imaging of apoptosis using confocal laser scanning microscopy and demonstrates the utility of the IID mechanism in live cells.
机译:在细胞表面上的外化磷脂酰丝氨酸(PS)的检测通常用于区分生物,凋亡和坏死细胞。 许多研究人员选择凋亡的选择工具是膜蛋白V-荧光团缀合物。 然而,使用该35kDa蛋白质与若干缺点相关,包括温度敏感性,Ca2 +依赖性和慢粘合动力学。 这里,描述了用于细胞表面PS,P-IID的荧光探针,其通过分子内指示剂位移(IID)机构操作。 在细胞表面PS存在下,分子内结合的香豆素指示剂释放,导致荧光“开启”反应。 与荧光成像和流式细胞术相比,P-IID在与annexin v相比时表现出优异的性能。 这允许P-IID使用共聚焦激光扫描显微镜进行细胞凋亡的时间延时成像,并证明了IID机制在活细胞中的效用。

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