Institute of Material Science and Engineering and Department of Mechanical Engineering and Material Science, Washington University in St. Louis, St Louis, 63130, MO, USA.
711th Human Performance Wing, Air Force Research Laboratory, Wright-Patterson, Air Force Base, Dayton, 45433, OH, USA.
Small. 2018 Feb;14(7). doi: 10.1002/smll.201702382. Epub 2018 Jan 11.
Interfacing biomolecules with functional materials is a key strategy toward achieving externally-triggered biological function. The rational integration of functional proteins, such as enzymes, with plasmonic nanostructures that exhibit unique optical properties such as photothermal effect provides a means to externally control the enzyme activity. However, due to the labile nature of enzymes, the photothermal effect of plasmonic nanostructures is mostly utilized for the enhancement of the biocatalytic activity of thermophilic enzymes. In order to extend and utilize the photothermal effect to a broader class of enzymes, a means to stabilize the immobilized active protein is essential. Inspired by biomineralization for the encapsulation of soft tissue within protective exteriors in nature, metal-organic framework is utilized to stabilize the enzyme. This strategy provides an effective route to enhance and externally modulate the biocatalytic activity of enzymes bound to functional nanostructures over a broad range of operating environments that are otherwise hostile to the biomolecules.
将生物分子与功能材料相连接是实现外部触发生物功能的关键策略。将具有独特光学特性(如光热效应)的功能蛋白(如酶)与等离子体纳米结构合理地整合在一起,为外部控制酶活性提供了一种手段。然而,由于酶的不稳定性,等离子体纳米结构的光热效应主要用于增强嗜热酶的生物催化活性。为了将光热效应扩展到更广泛的酶类,必须有一种稳定固定化活性蛋白的方法。受自然界中生物矿化将软组织封装在保护外壳内的启发,利用金属有机框架来稳定酶。该策略为在通常对生物分子不利的广泛操作环境下,增强和外部调节与功能纳米结构结合的酶的生物催化活性提供了一条有效途径。