Department School of Materials Science and Engineering and Research Institute for Solar and Sustainable Energies, Gwangju Institute of Science and Technology, 123 Cheomdan-gwagiro, Buk-gu, Gwangju, 61005, Korea.
Department of Polymer Science and Engineering, Chungnam National University, 299 Daehak-Ro, Yuseong-Gu, Daejeon, 34134, Korea.
Angew Chem Int Ed Engl. 2016 Sep 12;55(38):11495-8. doi: 10.1002/anie.201605609. Epub 2016 Aug 11.
The preparation of bicontinuous nanoporous covalent frameworks, which are promising for caging active enzymes, is demonstrated. The frameworks have three- dimensionally continuous, hydrophilic pores with widths varying between 5 and 30 nm. Enzymes were infiltrated into the bicontinuous pore by applying a pressured enzyme solution. The new materials and methods allowed the amount of caged proteins to be controlled precisely. The resulting enzyme-loaded framework films could be recycled many times with nearly no loss of catalytic activity. Entropic trapping of proteins by a bicontinuous pore with the right size distribution is an unprecedented strategy toward facile in vitro utilization of biocatalysts.
展示了用于固定活性酶的双连续纳米多孔共价骨架的制备方法。该骨架具有三维连续的亲水孔,宽度在 5 到 30nm 之间。通过施加加压酶溶液将酶渗透到双连续孔中。新材料和方法可以精确控制固定化蛋白质的量。所得的负载酶的框架膜可以多次回收,几乎没有催化活性的损失。通过具有适当尺寸分布的双连续孔对蛋白质进行熵捕获是一种前所未有的策略,可实现生物催化剂在体外的简便利用。