Balcioglu Mustafa, Buyukbekar Burak Zafer, Yavuz Mustafa Selman, Yigit Mehmet V
Department of Chemistry and The RNA Institute, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, United States.
Department of Metallurgy and Materials Engineering, Advanced Technology Research and Application Center, Selcuk University, Konya, Turkey.
ACS Biomater Sci Eng. 2015 Jan 12;1(1):27-36. doi: 10.1021/ab500029h. Epub 2014 Dec 4.
In this work, we have developed a general methodology for constructing an activatable biosensor utilizing a thermoresponsive polymer and two-dimensional nanosheet. We have demonstrated the detection of four different types of biological compounds using the smart PEGMA (poly(ethylene glycol) methyl ether methacrylate), oligonucleotides, and graphene oxide nanoassembly. The activity of the functional nanodevice is controlled with a thermo-switch at 39 °C. In this design, the nanosized graphene oxide serves as a template for fluorophore labeled probe oligonucleotides while quenching the fluorescence intensities dramatically. On the other hand, the PEGMA polymer serves as an activatable protecting layer covering the graphene oxide and entrapping the probe oligonucleotides on the surface. The PEGMA polymers are hydrophobic above their lower critical solution temperature (LCST) and therefore interact strongly with the hydrophobic surface of graphene oxide, creating a closed configuration (OFF state) of the nanodevice. However, once the temperature decreases below the LCST, the polymer undergoes conformational change and becomes hydrophilic. This opens up the surface of the graphene oxide (open configuration, ON state), freeing the encapsulated payload on the surface. We have tuned the activity of the nanodevice for the detection of a sequence-specific DNA, -10b, thrombin, and adenosine. The activity of our functional system can be decreased by ∼80% with a thermo-switch at 39 °C. Our approach can be extended to other antisense oligonucleotide, aptamer, or DNAzyme based sensing strategies.
在这项工作中,我们开发了一种通用方法,用于构建一种利用热响应聚合物和二维纳米片的可激活生物传感器。我们已经展示了使用智能聚(乙二醇)甲基醚甲基丙烯酸酯(PEGMA)、寡核苷酸和氧化石墨烯纳米组件检测四种不同类型生物化合物的方法。功能性纳米器件的活性通过39°C的热开关进行控制。在这种设计中,纳米尺寸的氧化石墨烯作为荧光团标记的探针寡核苷酸的模板,同时显著淬灭荧光强度。另一方面,PEGMA聚合物作为可激活的保护层覆盖氧化石墨烯,并将探针寡核苷酸捕获在表面。PEGMA聚合物在其下临界溶液温度(LCST)以上是疏水的,因此与氧化石墨烯的疏水表面强烈相互作用,形成纳米器件的封闭构型(关闭状态)。然而,一旦温度降至LCST以下,聚合物会发生构象变化并变得亲水。这会打开氧化石墨烯的表面(开放构型,开启状态),释放表面封装的有效载荷。我们已经对纳米器件的活性进行了调整,用于检测序列特异性DNA、-10b、凝血酶和腺苷。通过39°C的热开关,我们功能系统的活性可以降低约80%。我们的方法可以扩展到其他基于反义寡核苷酸、适体或DNA酶的传感策略。