Protein Encapsulation: A Nanocarrier Approach to the Fluorescence Imaging of an Enzyme-Based Biomarker

被引:23
作者
Jia, Zhiyuan [1 ,2 ]
Han, Hai-Hao [3 ,4 ]
Sedgwick, Adam C. [5 ]
Williams, George T. [6 ]
Gwynne, Lauren [6 ]
Brewster, James T., II [5 ]
Bull, Steven D. [6 ]
Jenkins, A. Toby A. [6 ]
He, Xiao-Peng [3 ,4 ]
Schoenherr, Holger [1 ,2 ]
Sessler, Jonathan L. [5 ]
James, Tony D. [6 ]
机构
[1] Univ Siegen, Phys Chem, Dept Chem & Biol, Siegen, Germany
[2] Univ Siegen, Res Ctr Micro & Nanochem & Engn C, Dept Chem & Biol, Siegen, Germany
[3] East China Univ Sci & Technol, Feringa Nobel Prize Scientist Joint Res Ctr, Sch Chem & Mol Engn, Key Lab Adv Mat, Shanghai, Peoples R China
[4] East China Univ Sci & Technol, Feringa Nobel Prize Scientist Joint Res Ctr, Sch Chem & Mol Engn, Joint Int Res Lab Precis Chem & Mol Engn, Shanghai, Peoples R China
[5] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
[6] Univ Bath, Dept Chem, Bath, Avon, England
基金
中国国家自然科学基金; 英国工程与自然科学研究理事会; 英国医学研究理事会; 欧洲研究理事会; 美国国家卫生研究院;
关键词
elastase detection; BSA-based nanocarrier; nanocarrier-based enzyme detection; fluorescence imaging; cell imaging; HUMAN NEUTROPHIL ELASTASE; THERAPEUTIC TARGET; PROBES; SUBSTRATE; DIAGNOSIS; DESIGN;
D O I
10.3389/fchem.2020.00389
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here, we report a new pentafluoropropanamido rhodamine fluorescent probe (ACS-HNE) that allows for the selective detection of neutrophil elastase (NE). ACS-HNE displayed high sensitivity, with a low limit of detection (<5.3 nM), and excellent selectivity toward elastase over other relevant biological analytes and enzymes. The comparatively poor solubility and cell permeability of neat ACS-HNE was improved by creating an ACS-HNE-albumin complex; this approach allowed for improvements in thein situvisualization of elastase activity in RAW 264.7 cells relative to ACS-HNE alone. The present study thus serves to demonstrate a simple universal strategy that may be used to overcome cell impermeability and solubility limitations, and to prepare probes suitable for the cellular imaging of enzymatic activityin vitro.
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页数:6
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