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Multiplex Detection of Protease Activity with Quantum Dot Nanosensors Prepared by Intein-Mediated Specific Bioconjugation

机译:蛋白质介导的特异性生物共轭制备的量子点纳米传感器对蛋白酶活性的多重检测。

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We report here a protease sensing nanoplatform based on semiconductor nanocrystals or quantum dots (QDs) and bioluminescence resonance energy transfer (QD-BRET) to detect the protease activity in complex biological samples. These nanosensors consist of bioluminescent proteins as the BRET donor, quantum dots as the BRET acceptor, and protease substrates sandwiched between the two as a sensing group. An intein-mediated conjugation strategy was developed for site-specific conjugation of proteins to QDs in preparing these QD nanosensors. In this traceless ligation, the intein itself is spliced out and excluded from the final conjugation product. With this method, we have synthesized a series of QD nanosensors for highly sensitive detection of an important class of protease matrix metalloproteinase (MMP) activity. We demonstrated that these nanosensors can detect the MMP activity in buffers and in mouse serum with the sensitivity to a few nanograms per milliliter and secreted proteases by tumor cells. The suitability of these nanosensors for a multiplex protease assay has also been shown.
机译:我们在这里报告基于半导体纳米晶体或量子点(QDs)和生物发光共振能量转移(QD-BRET)的蛋白酶感测纳米平台,以检测复杂生物样品中的蛋白酶活性。这些纳米传感器由生物发光蛋白(作为BRET供体),量子点(作为BRET受体)和夹在两者之间的蛋白酶底物作为传感基团组成。开发了一种内含蛋白介导的偶联策略,用于在制备这些QD纳米传感器时将蛋白质与QD进行位点特异性偶联。在这种无痕的连接中,内含肽本身被剪接并从最终的偶联产物中排除。通过这种方法,我们合成了一系列QD纳米传感器,用于高灵敏度检测重要类别的蛋白酶基质金属蛋白酶(MMP)活性。我们证明了这些纳米传感器可以检测缓冲液和小鼠血清中的MMP活性,对每毫升几纳克的敏感性以及肿瘤细胞分泌的蛋白酶的敏感性。还显示了这些纳米传感器对多重蛋白酶测定的适用性。

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