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肽核酸 (PNA)-引导的适体传感器的肽工程用于蛋白酶触发的分子成像。

Peptide Nucleic Acid (PNA)-Guided Peptide Engineering of an Aptamer Sensor for Protease-Triggered Molecular Imaging.

机构信息

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, 100190, China.

College of Materials Science and Optoelectronic Technology, University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Angew Chem Int Ed Engl. 2021 Oct 11;60(42):22659-22663. doi: 10.1002/anie.202106639. Epub 2021 Sep 12.

Abstract

Protease-triggered control of functional DNA has remained unachieved, leaving a significant gap in activatable DNA biotechnology. Herein, we report the design of a protease-activatable aptamer system that can perform molecular sensing and imaging in a tumor-specific manner. The system is constructed by locking the structure-switching activity of an aptamer using a rationally designed PNA-peptide-PNA triblock copolymer. Highly selective protease-mediated cleavage of the peptide substrate results in reduced binding affinity of PNA to the aptamer module, with the subsequent recovery of its biosensing function. We demonstrated that the DNA/peptide/PNA hybrid system allows for tumor cell-selective ATP imaging in vitro and also produces a fluorescent signal in vivo with improved tumor specificity. This work illustrates the potential of bridging the gap between functional DNA and peptides for precise biomedical applications.

摘要

蛋白酶触发的功能性 DNA 控制仍然难以实现,这在可激活 DNA 生物技术方面留下了很大的空白。在此,我们报告了一种蛋白酶激活适体系统的设计,该系统可以以肿瘤特异性的方式进行分子传感和成像。该系统通过使用合理设计的 PNA-肽-PNA 三嵌段共聚物锁定适体的结构切换活性来构建。高度选择性的蛋白酶介导的肽底物切割导致 PNA 与适体模块的结合亲和力降低,随后恢复其生物传感功能。我们证明,DNA/肽/PNA 杂合系统允许在体外进行肿瘤细胞选择性的 ATP 成像,并且还可以在体内产生荧光信号,提高了肿瘤特异性。这项工作说明了在功能 DNA 和肽之间架起桥梁以实现精确的生物医学应用的潜力。

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