National Engineering Research Center for Biomaterials, Sichuan University, 29 Wangjiang Road, Chengdu 610064, China.
College of Materials Science and Engineering, Sichuan University, 29 Wangjiang Road, Chengdu 610064, China.
Nano Lett. 2020 Sep 9;20(9):6548-6555. doi: 10.1021/acs.nanolett.0c02298. Epub 2020 Aug 7.
Artificial organelles (AOs) are typical microcompartments with intracellular biocatalytic activity aimed to replace missing or lost cellular functions. Currently, liposomes or polymersomes are popular microcompartments to build AOs by embedding channel proteins in their hydrophobic domain and entrapping natural enzymes in their cavity. Herein, a new microcompartment is established by using monolayer cross-linked zwitterionic vesicles (cZVs) with a carboxylic acid saturated cavity. The monolayer structure endows the cZVs with intrinsic permeability; the cavity supplies the cZVs ability of synthesis of artificial enzymes, and the pH-dependent charge-change property makes it possible to overcome the biological barriers. Typically, nanozymes of CeO and Pt NPs were synthesized in the cZVs to mimic peroxisome. experiments confirmed that the resulting artificial peroxisome (AP) could resist protein adsorption, endocytose efficiently, and escape from the lysosome. experiments demonstrated that the APs held a good therapeutic effect in ROS-induced ear-inflammation.
人工细胞器 (AOs) 是具有细胞内生物催化活性的典型微区室,旨在替代缺失或丧失的细胞功能。目前,脂质体或聚合物体是通过将通道蛋白嵌入其疏水区并将天然酶包埋在其腔中来构建 AOs 的常用微区室。本文通过使用具有饱和羧酸腔的单层交联两性离子囊泡 (cZVs) 建立了一种新的微区室。单层结构赋予 cZVs 固有通透性;腔赋予 cZVs 合成人工酶的能力,并且 pH 依赖性电荷变化特性使得克服生物屏障成为可能。通常,CeO 和 Pt NPs 的纳米酶在 cZVs 中合成以模拟过氧化物酶体。实验证实,所得的人工过氧化物酶体 (AP) 能够抵抗蛋白吸附,有效内吞,并从溶酶体中逃逸。实验表明,AP 在 ROS 诱导的耳炎中具有良好的治疗效果。