Cai Ren, Yang Dan, Peng Shengjie, Chen Xigao, Huang Yun, Liu Yuan, Hou Weijia, Yang Shengyuan, Liu Zhenbao, Tan Weihong
Center for Research at Bio/Nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, Health Cancer Center, UF Genetics Institute and McKnight Brain Institute, University of Florida , Gainesville, Florida 32611-7200, United States.
School of Materials Science and Engineering, Nanyang Technological University , 50 Nanyang Avenue, Singapore 639798.
J Am Chem Soc. 2015 Nov 4;137(43):13957-63. doi: 10.1021/jacs.5b09337. Epub 2015 Oct 23.
A facile strategy has been developed to fabricate Cu(OH)2 supercages (SCs) as an artificial enzyme system with intrinsic peroxidase-mimic activities (PMA). SCs with high catalytic activity and excellent recyclability were generated via direct conversion of amorphous Cu(OH)2 nanoparticles (NPs) at room temperature. More specifically, the process that takes a single nanoparticle to a 3D supercage involves two basic steps. First, with addition of a copper-ammonia complex, the Cu(2+) ions that are located on the surface of amorphous Cu(OH)2 NPs would evolve into a fine lamellar structure by coordination and migration and eventually convert to 1D nanoribbons around the NPs. Second, accompanied by the migration of Cu(2+), a hollow cavity is generated in the inner NPs, such that a single nanoparticle eventually becomes a nanoribbon-assembled 3D hollow cage. These Cu(OH)2 SCs were then engineered as an artificial enzymatic system with higher efficiency for intrinsic PMA than the peroxidase activity of a natural enzyme, horseradish peroxidase.
已开发出一种简便策略来制备作为具有内在过氧化物酶模拟活性(PMA)的人工酶系统的氢氧化铜超笼(SCs)。通过在室温下将无定形氢氧化铜纳米颗粒(NPs)直接转化生成具有高催化活性和优异可回收性的SCs。更具体地说,将单个纳米颗粒转变为三维超笼的过程涉及两个基本步骤。首先,添加铜氨配合物后,位于无定形氢氧化铜NPs表面的铜离子通过配位和迁移演变成精细的层状结构,并最终在NPs周围转化为一维纳米带。其次,伴随着铜离子的迁移,内部NPs中产生一个中空腔,使得单个纳米颗粒最终变成由纳米带组装而成的三维中空笼。然后将这些氢氧化铜SCs设计成一种人工酶系统,其内在PMA效率高于天然酶辣根过氧化物酶的过氧化物酶活性。