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不同疏水性聚电解质复合物的蛋白质冠研究——从方法开发到体外研究。

Protein corona investigations of polyplexes with varying hydrophobicity - From method development to in vitro studies.

机构信息

Ludwig-Maximilians-University, Pharmaceutical Technology and Biopharmaceutics, Butenandtstr. 5-13, 81377 Munich, Germany.

Metbolomics and Proteomics Core, Helmholtz Zentrum München, German Research Center for Environmental Health GmbH, Heidemannsstr. 1, 80939 Munich, Germany.

出版信息

Int J Pharm. 2023 Aug 25;643:123257. doi: 10.1016/j.ijpharm.2023.123257. Epub 2023 Jul 22.

DOI:10.1016/j.ijpharm.2023.123257
PMID:37482228
Abstract

In the field of non-viral drug delivery, polyplexes (PXs) represent an advanced investigated and highly promising tool for the delivery of nucleic acids. Upon encountering physiological fluids, they adsorb biological molecules to form a protein corona (PC), that influence PXs biodistribution, transfection efficiencies and targeting abilities. In an effort to understand protein - PX interactions and the effect of PX material on corona composition, we utilized cationic branched 10 kDa polyethyleneimine (b-PEI) and a hydrophobically modified nylon-3 polymer (NM/CP) within this study to develop appropriate methods for PC investigations. A centrifugation procedure for isolating hard corona - PX complexes (PCPXs) from soft corona proteins after incubating the PXs in fetal bovine serum (FBS) for PC formation was successfully optimized and the identification of proteins by a liquid chromatography-tandem mass spectrometry (LC-MS-MS) method clearly demonstrated that the PC composition is affected by the underlying PXs material. With regard to especially interesting functional proteins, which might be able to induce active targeting effects, several candidates could be detected on b-PEI and NM/CP PXs. These results are of high interest to better understand how the design of PXs impacts the PC composition and subsequently PCPXs-cell interactions to enable precise adjustment of PXs for targeted drug delivery.

摘要

在非病毒药物递送领域,多聚物(PXs)是一种经过深入研究且极具应用前景的核酸递送工具。在遇到生理体液时,它们会吸附生物分子形成蛋白质外壳(PC),从而影响 PXs 的生物分布、转染效率和靶向能力。为了深入了解蛋白质与 PXs 的相互作用以及 PXs 材料对其外壳组成的影响,本研究采用阳离子支化 10 kDa 聚乙烯亚胺(b-PEI)和疏水性改性尼龙-3 聚合物(NM/CP),开发了合适的方法来研究 PC。成功优化了一种离心程序,用于在胎牛血清(FBS)中孵育 PX 以形成 PC 后,从软壳蛋白中分离硬壳-PX 复合物(PCPXs),并通过液相色谱-串联质谱(LC-MS-MS)方法鉴定蛋白质,明确证明了 PC 的组成受 PXs 材料的影响。关于可能诱导主动靶向作用的特别有趣的功能蛋白,在 b-PEI 和 NM/CP PXs 上可以检测到几个候选蛋白。这些结果对于深入了解 PXs 的设计如何影响 PC 组成,以及随后 PCPXs-细胞相互作用,从而能够精确调整 PXs 以实现靶向药物递送具有重要意义。

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