Department of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, Massachusetts 01003, United States.
Key Laboratory for Green Process of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003, People's Republic of China.
J Am Chem Soc. 2020 Jun 17;142(24):10723-10729. doi: 10.1021/jacs.0c01758. Epub 2020 Jun 8.
Bioorthogonal catalysis offers a unique strategy to modulate biological processes through the in situ generation of therapeutic agents. However, the direct application of bioorthogonal transition metal catalysts (TMCs) in complex media poses numerous challenges due to issues of limited biocompatibility, poor water solubility, and catalyst deactivation in biological environments. We report here the creation of catalytic "polyzymes", comprised of self-assembled polymer nanoparticles engineered to encapsulate lipophilic TMCs. The incorporation of catalysts into these nanoparticle scaffolds creates water-soluble constructs that provide a protective environment for the catalyst. The potential therapeutic utility of these nanozymes was demonstrated through antimicrobial studies in which a cationic nanozyme was able to penetrate into biofilms and eradicate embedded bacteria through the bioorthogonal activation of a pro-antibiotic.
生物正交催化提供了一种独特的策略,可通过原位生成治疗剂来调节生物过程。然而,由于生物相容性有限、水溶性差以及在生物环境中催化剂失活等问题,直接应用生物正交过渡金属催化剂(TMCs)在复杂介质中面临着诸多挑战。我们在此报告了催化“多酶”的创建,该多酶由自组装聚合物纳米粒子组成,设计用于封装亲脂性 TMCs。将催化剂纳入这些纳米粒子支架中,可形成水溶性结构,为催化剂提供保护环境。通过抗菌研究证明了这些纳米酶的潜在治疗用途,其中阳离子纳米酶能够穿透生物膜,并通过前抗生素的生物正交激活来消除嵌入的细菌。