School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, Jiangsu, PR China.
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, Jiangsu, PR China.
J Colloid Interface Sci. 2021 Oct 15;600:37-48. doi: 10.1016/j.jcis.2021.05.025. Epub 2021 May 8.
Recently, nanozymes have attracted sustained attention for facilitating next generation of artificial enzymatic cascade systems (ECSs). However, the fabrication of integrated multi-ECSs based on a single nanozyme remains a great challenge. Here, inspired by the biological function and self-assembling ability of arginine (R), we synthesized arginine-rich peptide-Pt nanoparticle cluster (ARP-PtNC) nanozymes that mimic two typical enzymatic cascade systems of uricase/catalase and superoxide dismutase/catalase in natural peroxisome. ARPs containing at least 10 arginine residues contribute to the cluster formation based on hydrogen bonding and coordination. The well-designed peptide-Pt hybrid nanozyme not only possesses excellent uricase-mimicking activity to degrade uric acid effectively, but also serves as a desired scavenger for reactive oxygen species (ROS) harnessing two efficient enzyme cascade catalysis of uricase/catalase and superoxide dismutase/catalase. The surface microenvironment of the hybrid nanozymes provided by arginine-rich peptides and the cluster structure contribute to the efficient multiply enzyme-like activities. Fascinatingly, the hybrid nanozyme can inhibit the formation of monosodium urate monohydrate effectively based on the architecture of ARP-PtNCs. Thus, ARP-PtNC nanozyme has the potential in gout and hyperuricemia therapy. Rational design of ingenious peptide-metal hybrid nanozyme with unique physicochemical surface properties provides a versatile and designed strategy to fabricate multi-enzymatic cascade systems, which opens new avenues to broaden the application of nanozymes in practice.
最近,纳米酶因其能够促进下一代人工酶级联系统 (ECSs) 的发展而受到持续关注。然而,基于单个纳米酶构建集成的多 ECS 仍然是一个巨大的挑战。在这里,受精氨酸 (R) 的生物学功能和自组装能力的启发,我们合成了富含精氨酸的肽-铂纳米颗粒簇 (ARP-PtNC) 纳米酶,模拟了天然过氧化物酶体中尿酸酶/过氧化氢酶和超氧化物歧化酶/过氧化氢酶两种典型的酶级联系统。至少含有 10 个精氨酸残基的 ARP 有助于基于氢键和配位的簇形成。这种经过精心设计的肽-铂杂化纳米酶不仅具有出色的尿酸酶模拟活性,可有效降解尿酸,而且还可作为活性氧 (ROS) 的理想清除剂,利用尿酸酶/过氧化氢酶和超氧化物歧化酶/过氧化氢酶的两种高效酶级联催化作用。富含精氨酸的肽和簇结构为其提供的杂化纳米酶的表面微环境有助于其高效的多酶样活性。有趣的是,杂化纳米酶可以基于 ARP-PtNC 的结构有效抑制单水合尿酸单钠的形成。因此,ARP-PtNC 纳米酶有望用于痛风和高尿酸血症的治疗。具有独特物理化学表面特性的巧妙肽-金属杂化纳米酶的合理设计为构建多酶级联系统提供了一种通用且经过设计的策略,为纳米酶在实际应用中的广泛应用开辟了新途径。