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Detecting protease activity

机译:检测蛋白酶活性

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Zeev Rosenzweig and colleagues at the University of New Orleans recently modified quantum dots (QDs) to develop a sensor that intrinsically measures the activity of matrix metallo-proteinases (MMPs) in normal and cancerous tissues. In this fluorescence resonance energy transfer assay, the acceptors were rhodamine molecules rather than gold nanoparticles. The rhodamines were attached to the QDs (the donors) via tetrapeptides of RGDC. In the absence of proteases, excited QDs emitted red light (590 nm). When the tetrapeptides were cleaved by the protease, the rhodamine molecules were released, and the QD emission changed to green light (545 nm).
机译:新奥尔良大学的Zeev Rosenzweig及其同事最近修改了量子点(QD),以开发一种传感器,该传感器可固有地测量正常组织和癌性组织中基质金属蛋白酶(MMP)的活性。在这种荧光共振能量转移测定中,受体是若丹明分子而不是金纳米颗粒。罗丹明通过RGDC的四肽与QDs(供体)相连。在没有蛋白酶的情况下,激发的量子点发出红光(590 nm)。当四肽被蛋白酶切割时,若丹明分子被释放,QD发射变为绿光(545 nm)。

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