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可编程肽交联核酸纳米胶囊作为酶特异性货物释放的模块化平台

Programmable Peptide-Cross-Linked Nucleic Acid Nanocapsules as a Modular Platform for Enzyme Specific Cargo Release.

作者信息

Santiana Joshua J, Sui Binglin, Gomez Nicole, Rouge Jessica L

机构信息

Department of Chemistry, University of Connecticut , Storrs, Connecticut 06269, United States.

出版信息

Bioconjug Chem. 2017 Dec 20;28(12):2910-2914. doi: 10.1021/acs.bioconjchem.7b00629. Epub 2017 Nov 30.

Abstract

Herein we describe a modular assembly strategy for photo-cross-linking peptides into nucleic acid functionalized nanocapsules. The peptides embedded within the nanocapsules form discrete nanoscale populations capable of gating the release of molecular and nanoscale cargo using enzyme-substrate recognition as a triggered release mechanism. Using photocatalyzed thiol-yne chemistry, different peptide cross-linkers were effectively incorporated into the nanocapsules and screened against different proteases to test for degradation specificity both in vitro and in cell culture. By using a combination of fluorescence assays, confocal and TEM microscopy, the particles were shown to be highly specific for their enzyme targets, even between enzymes of similar protease classes. The rapid and modular nature of the assembly strategy has the potential to be applied to both intracellular and extracellular biosensing and drug delivery applications.

摘要

在此,我们描述了一种用于将光交联肽组装到核酸功能化纳米胶囊中的模块化组装策略。嵌入纳米胶囊内的肽形成离散的纳米级群体,能够利用酶-底物识别作为触发释放机制来控制分子和纳米级货物的释放。通过光催化硫醇-炔化学,不同的肽交联剂被有效地整合到纳米胶囊中,并针对不同的蛋白酶进行筛选,以在体外和细胞培养中测试降解特异性。通过结合荧光测定、共聚焦和透射电子显微镜,这些颗粒被证明对其酶靶标具有高度特异性,即使在相似蛋白酶类别的酶之间也是如此。这种组装策略的快速性和模块化性质有可能应用于细胞内和细胞外生物传感及药物递送应用。

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