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脂质体蛋白冠的特性分析——纳米医学的新方法

Liposome protein corona characterization as a new approach in nanomedicine.

机构信息

Department of Chemistry, Sapienza Università di Roma, Piazzale Aldo Moro 5, 00185, Rome, Italy.

出版信息

Anal Bioanal Chem. 2019 Jul;411(19):4313-4326. doi: 10.1007/s00216-019-01656-x. Epub 2019 Feb 13.

Abstract

This trends article describes the analytical approaches for the in-depth characterization of the protein corona on liposome nanoparticles. In particular, examples since 2014 are summarized according to the analytical approach. Traditional protein corona characterizations from in vitro static experiments are provided along with the newly introduced experimental setups for characterization of the protein corona by in vitro dynamic and in vivo studies. Additionally, a special attention is also devoted to the need for introduction of new experimental workflows for characterization of a much wider array of biomolecules. In the most recent years, an extension of the protein corona concept to the biomolecular corona was introduced, and the analytical targets are no longer restricted to proteins, but to other important biomolecules as well, as they can potentially affect the biodistribution and interaction of nanoparticles with the biological systems. The few recent examples in this field are discussed for the characterization of metabolites and lipids in the biomolecular corona with examples, also extending the discussion from liposome to other types of nanoparticles. A final discussion is provided on the potential key role of the most recent omics approaches in the study of the nano-bio interface, with an overview on top-down proteomics, which allows a better elucidation of proteoforms, and on lipidomics and metabolomics, which allow a comprehensive untargeted characterization of lipids and metabolites, respectively. Graphical abstract.

摘要

这篇综述文章描述了深入分析脂质体纳米粒子蛋白冠的分析方法。特别是,根据分析方法总结了自 2014 年以来的实例。本文提供了传统的体外静态实验的蛋白冠特征,以及新引入的用于体外动态和体内研究的蛋白冠特征的实验方案。此外,还特别关注需要引入新的实验工作流程来表征更广泛的生物分子。在最近几年,蛋白冠概念被扩展到生物分子冠,分析目标不再仅限于蛋白质,还包括其他重要的生物分子,因为它们可能会影响纳米粒子与生物系统的生物分布和相互作用。本文还讨论了该领域的一些最新实例,用于表征生物分子冠中的代谢物和脂质,同时将讨论从脂质体扩展到其他类型的纳米粒子。最后,本文还讨论了组学方法在纳米生物界面研究中的潜在关键作用,概述了自上而下的蛋白质组学,它可以更好地阐明蛋白异构体,以及脂质组学和代谢组学,它们可以分别对脂质和代谢物进行全面的非靶向特征分析。

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