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用蛋白质冠层包裹隐形纳米粒子进行靶向药物递送。

Cloaking nanoparticles with protein corona shield for targeted drug delivery.

机构信息

Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.

Department of Biological Sciences, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.

出版信息

Nat Commun. 2018 Oct 31;9(1):4548. doi: 10.1038/s41467-018-06979-4.


DOI:10.1038/s41467-018-06979-4
PMID:30382085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6208370/
Abstract

Targeted drug delivery using nanoparticles can minimize the side effects of conventional pharmaceutical agents and enhance their efficacy. However, translating nanoparticle-based agents into clinical applications still remains a challenge due to the difficulty in regulating interactions on the interfaces between nanoparticles and biological systems. Here, we present a targeting strategy for nanoparticles incorporated with a supramolecularly pre-coated recombinant fusion protein in which HER2-binding affibody combines with glutathione-S-transferase. Once thermodynamically stabilized in preferred orientations on the nanoparticles, the adsorbed fusion proteins as a corona minimize interactions with serum proteins to prevent the clearance of nanoparticles by macrophages, while ensuring systematic targeting functions in vitro and in vivo. This study provides insight into the use of the supramolecularly built protein corona shield as a targeting agent through regulating the interfaces between nanoparticles and biological systems.

摘要

利用纳米粒子进行靶向药物输送可以最小化传统药物制剂的副作用,并提高其疗效。然而,将基于纳米粒子的制剂转化为临床应用仍然是一个挑战,因为难以调节纳米粒子与生物系统界面上的相互作用。在这里,我们提出了一种靶向策略,即将包含超分子预涂层重组融合蛋白的纳米粒子,其中 HER2 结合亲和体与谷胱甘肽-S-转移酶结合。一旦在纳米粒子上以优先取向热力学稳定,吸附的融合蛋白作为一个冠层,最大限度地减少与血清蛋白的相互作用,以防止纳米粒子被巨噬细胞清除,同时确保在体外和体内的系统靶向功能。这项研究为通过调节纳米粒子与生物系统界面来使用超分子构建的蛋白质冠作为靶向剂提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/a97f1724cb51/41467_2018_6979_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/5912da316105/41467_2018_6979_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/ea8f9f2d5a07/41467_2018_6979_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/ec22fbb35bee/41467_2018_6979_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/a97f1724cb51/41467_2018_6979_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/5912da316105/41467_2018_6979_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/ea8f9f2d5a07/41467_2018_6979_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/ec22fbb35bee/41467_2018_6979_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c2/6208370/a97f1724cb51/41467_2018_6979_Fig4_HTML.jpg

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本文引用的文献

[1]
Clinically approved liposomal nanomedicines: lessons learned from the biomolecular corona.

Nanoscale. 2018-3-1

[2]
A Decade of the Protein Corona.

ACS Nano. 2017-12-5

[3]
An apolipoprotein-enriched biomolecular corona switches the cellular uptake mechanism and trafficking pathway of lipid nanoparticles.

Nanoscale. 2017-11-16

[4]
Molecularly Imprinted Nanogels Acquire Stealth In Situ by Cloaking Themselves with Native Dysopsonic Proteins.

Angew Chem Int Ed Engl. 2017-4-28

[5]
Unveiling the in Vivo Protein Corona of Circulating Leukocyte-like Carriers.

ACS Nano. 2017-3-10

[6]
Mapping of Molecular Structure of the Nanoscale Surface in Bionanoparticles.

J Am Chem Soc. 2016-12-29

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Regulation of Macrophage Recognition through the Interplay of Nanoparticle Surface Functionality and Protein Corona.

ACS Nano. 2016-4-26

[8]
Protein adsorption is required for stealth effect of poly(ethylene glycol)- and poly(phosphoester)-coated nanocarriers.

Nat Nanotechnol. 2016-2-15

[9]
Nanoparticle-blood interactions: the implications on solid tumour targeting.

Chem Commun (Camb). 2015-2-18

[10]
Impact of protein pre-coating on the protein corona composition and nanoparticle cellular uptake.

Biomaterials. 2015-10-9

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