Lin Yiyang, Chapman Robert, Stevens Molly M
Department of Materials, Department of Bioengineering and Institute for Biomedical Engineering, Imperial College London, Exhibition Road, London SW7 2AZ, UK.
Adv Funct Mater. 2015 Jun 1;25(21):3183-3192. doi: 10.1002/adfm.201500624.
Hybrid self-assembly has become a reliable approach to synthesize soft materials with multiple levels of structural complexity and synergistic functionality. In this work, photoluminescent graphene quantum dots (GQDs, 2-5 nm) are used for the first time as molecule-like building blocks to construct self-assembled hybrid materials for label-free biosensors. Ionic self-assembly of disc-shaped GQDs and charged biopolymers is found to generate a series of hierarchical structures that exhibit aggregation-induced fluorescence quenching of the GQDs and change the protein/polypeptide secondary structure. The integration of GQDs and biopolymers via self-assembly offers a flexible toolkit for the design of label-free biosensors in which the GQDs serve as a fluorescent probe and the biopolymers provide biological function. The versatility of this approach is demonstrated in the detection of glycosaminoglycans (GAGs), pH, and proteases using three strategies: 1) competitive binding of GAGs to biopolymers, 2) pH-responsive structural changes of polypeptides, and 3) enzymatic hydrolysis of the protein backbone, respectively. It is anticipated that the integrative self-assembly of biomolecules and GQDs will open up new avenues for the design of multifunctional biomaterials with combined optoelectronic properties and biological applications.
混合自组装已成为一种可靠的方法,用于合成具有多层次结构复杂性和协同功能的软材料。在这项工作中,首次使用光致发光石墨烯量子点(GQDs,2 - 5纳米)作为类似分子的构建单元,构建用于无标记生物传感器的自组装混合材料。发现盘状GQDs与带电生物聚合物的离子自组装会产生一系列分级结构,这些结构表现出GQDs的聚集诱导荧光猝灭,并改变蛋白质/多肽的二级结构。通过自组装将GQDs与生物聚合物整合,为设计无标记生物传感器提供了一个灵活的工具包,其中GQDs用作荧光探针,生物聚合物提供生物学功能。这种方法的多功能性在使用三种策略检测糖胺聚糖(GAGs)、pH值和蛋白酶时得到了证明:1)GAGs与生物聚合物的竞争性结合,2)多肽的pH响应结构变化,以及3)蛋白质主链的酶促水解。预计生物分子与GQDs的整合自组装将为设计具有组合光电特性和生物学应用的多功能生物材料开辟新途径。