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多功能超分子复合物用于靶向抗菌光动力失活。

Versatile Supramolecular Complex for Targeted Antimicrobial Photodynamic Inactivation.

机构信息

Dipartimento di Scienze Matematiche, Fisiche e Informatiche, Università di Parma, Parco Area delle Scienze 7A, Parma 43124, Italy.

Nanoscopy@Istituto Italiano di Tecnologia, Via Enrico Melen 83B, Genova 16152, Italy.

出版信息

Bioconjug Chem. 2022 Apr 20;33(4):666-676. doi: 10.1021/acs.bioconjchem.2c00067. Epub 2022 Mar 10.

Abstract

We report the development of a supramolecular structure endowed with photosensitizing properties and targeting capability for antimicrobial photodynamic inactivation. Our synthetic strategy uses the tetrameric bacterial protein streptavidin, labeled with the photosensitizer eosin, as the main building block. Biotinylated immunoglobulin G (IgG) from human serum, known to associate with protein A, was bound to the complex streptavidin-eosin. Fluorescence correlation spectroscopy and fluorescence microscopy demonstrate binding of the complex to . Efficient photoinactivation is observed for suspensions treated with IgG-streptavidin-eosin at concentrations higher than 0.5 μM and exposed to green light. The proposed strategy offers a flexible platform for targeting a variety of molecules and microbial species.

摘要

我们报告了一种具有光敏性质和靶向能力的超分子结构的开发,用于抗菌光动力失活。我们的合成策略使用四聚体细菌蛋白链霉亲和素,标记有光敏剂曙红,作为主要构建块。与人血清中的免疫球蛋白 G(IgG)结合的生物素化 IgG,已知与蛋白 A 结合,被结合到链霉亲和素-曙红复合物上。荧光相关光谱和荧光显微镜证明了该复合物与人血清中的免疫球蛋白 G(IgG)结合。当用浓度高于 0.5 μM 的 IgG-链霉亲和素-曙红处理并暴露于绿光时,观察到对 的高效光灭活。所提出的策略为靶向各种分子和微生物物种提供了一个灵活的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba77/9026257/d05bea636694/bc2c00067_0002.jpg

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