Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Angew Chem Int Ed Engl. 2010 Dec 10;49(50):9648-51. doi: 10.1002/anie.201005243.
are available in large amounts using dual expression vectors that guide the preparation of Qβ virus-like particles encapsulating multiple copies of functional enzymes. Packaging is promoted by RNA aptamer sequences that bridge between the coat protein and a peptide tag fused to the desired cargo. Peptidase E and luciferase were thus encapsulated and shown to be catalytically active inside the particle. The encapsulated enzymes are less sensitive to inactivation by heating and surface adsorption than the corresponding free enzymes. This system represents a modular way to marry catalytic activity with robust scaffolding for the development of multifunctional materials.
该方法使用双表达载体大量制备 Qβ 病毒样颗粒,这些颗粒可包裹多个功能酶分子。通过连接衣壳蛋白和融合到所需货物上的肽标签的 RNA 适体序列促进包装。因此,蛋白酶 E 和荧光素酶被包裹在内,并且在颗粒内部表现出催化活性。与相应的游离酶相比,包封的酶对加热和表面吸附的失活作用不那么敏感。该系统代表了一种将催化活性与稳健的支架结合起来用于开发多功能材料的模块化方法。