Hyziuk Pavlo, Flaibani Matteo, Posocco Paola, Sashuk Volodymyr
Institute of Physical Chemistry, Polish Academy of Sciences Kasprzaka 44/52 01-224 Warsaw Poland
Department of Engineering and Architecture, University of Trieste Via Alfonso Valerio, n. 6/A 34127 Trieste Italy
Chem Sci. 2024 Sep 26;15(40):16480-4. doi: 10.1039/d4sc04577g.
Enzyme mimics, due to their limited complexity, traditionally display low catalytic efficiency. Herein we present a strategy that enables the transformation of a slow-acting catalyst into a highly active one by creating a non-covalent suprastructure, termed "suprazyme". We show that cucurbit[7]uril macrocycles, rudimentary molecular enzyme mimics, embedded within an anionic monolayer on the surface of gold nanoparticles, outperform individual cucurbit[7]urils as well as nanoparticles, which also exhibit catalytic enzyme-like activity and thus act as nanozymes, by over 50 times, showcasing a 1044-fold acceleration in a model oxime formation reaction. The superior performance of such a suprazyme is attributed to a synergistic interplay between the organic monolayer and macrocycles, which is accompanied by a decreased local polarity and pH that favors the acid-catalyzed condensation process. The proposed approach holds promise for developing diverse suprazymes, contingent upon achieving a complementary structure and mechanism of action between the molecular catalyst and nanoparticles.
由于其复杂性有限,传统的酶模拟物催化效率较低。在此,我们提出了一种策略,通过创建一种称为“超酶”的非共价超结构,将一种作用缓慢的催化剂转化为高活性催化剂。我们表明,嵌入金纳米颗粒表面阴离子单层中的葫芦[7]脲大环(基本的分子酶模拟物),在模型肟形成反应中表现出比单个葫芦[7]脲以及同样具有类酶催化活性的纳米颗粒(即纳米酶)高出50倍以上的性能,加速了1044倍。这种超酶的卓越性能归因于有机单层和大环之间的协同相互作用,同时伴随着局部极性和pH值的降低,这有利于酸催化的缩合过程。所提出的方法有望开发出多种超酶,这取决于分子催化剂和纳米颗粒之间实现互补的结构和作用机制。