带有可更换夹子的DNA镊子用于细胞膜蛋白的靶向降解。

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Yang Sun, Yichen Huang, Daiquan Chen, Shangjiu Hu, Tao Pan, Yuanding Liu, Ruowen Wang, Weihong Tan
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引用次数: 0

摘要

背景:细胞膜蛋白在信号转导和营养转运中起着重要作用。据报道,许多膜蛋白在癌细胞中过度表达,这与癌症的进展密切相关。这些膜蛋白的靶向降解已被证明是一种很有前途的肿瘤治疗策略。利用适体介导膜蛋白裂解的几种策略,如溶酶体介导的裂解和蛋白酶体介导的裂解,已被报道,但它们的效率受到适体与单一靶标的结合亲和力的限制。方法:构建可更换夹钳的DNA镊子,更换夹钳后可裂解不同的蛋白质。此外,夹子通过增强特异性和提高结合亲和力,提高了靶蛋白的降解效率。结果:在不同肿瘤细胞系中均有裂解作用,并在斑马鱼中有抗肿瘤活性。结论:总的来说,这些DNA镊子提高了功能性核酸靶向递送的效率,为致病蛋白的降解提供了一种高效和通用的策略,并扩大了抗肿瘤治疗的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA Tweezers with Replaceable Clamps for the Targeted Degradation of Cell Membrane Proteins.

Background: Cell membrane proteins play crucial roles in signal transduction and nutrient transport. Many membrane proteins are reportedly overexpressed in cancer cells, which is closely related to cancer progression. The targeted degradation of these membrane proteins has been demonstrated to be a promising strategy for tumor treatment. Several strategies using aptamers to mediate membrane protein lysis, such as lysosomal-mediated lysis and proteasome-mediated lysis, have been reported, but their efficiency is limited by the binding affinity of the aptamer to a single target. Methods: We constructed DNA tweezers with replaceable clamps, which can lyse different proteins upon clamp replacement. Moreover, the clamp improved the degradation efficiency of the target proteins by enhancing the specificity and improving the binding affinity. Results: Lysis was verified in different tumor cell lines and the antitumor activity was confirmed in zebrafish. Conclusions: Overall, these DNA tweezers improve the efficiency of the targeted delivery of functional nucleic acids, provide an efficient and versatile strategy for the degradation of disease-causing proteins, and expand the approach to antitumor therapy.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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