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金纳米颗粒穿透脂质膜:细胞摄取、细胞毒性及其关系的深入了解。

Penetration of lipid membranes by gold nanoparticles: insights into cellular uptake, cytotoxicity, and their relationship.

机构信息

State Key Laboratory of Structure Analysis for Industrial Equipment, Department of Engineering Mechanics, Faculty of Vehicle Engineering and Mechanics, Dalian University of Technology, Dalian 116024, P. R. China.

出版信息

ACS Nano. 2010 Sep 28;4(9):5421-9. doi: 10.1021/nn1010792.

Abstract

Nanoparticle penetration into cell membranes is an interesting phenomenon that may have crucial implications on the nanoparticles' biomedical applications. In this paper, a coarse-grained model for gold nanoparticles (AuNPs) is developed (verified against experimental data available) to simulate their interactions with model lipid membranes. Simulations reveal that AuNPs with different signs and densities of surface charges spontaneously adhere to the bilayer surface or penetrate into the bilayer interior. The potential of mean force calculations show that the energy gains upon adhesion or penetration is significant. In the case of penetration, it is found that defective areas are induced across the entire surface of the upper leaflet of the bilayer and a hydrophilic pore that transports water molecules was formed with its surrounding lipids highly disordered. Penetration and its concomitant membrane disruptions can be a possible mechanism of the two observed phenomena in experiments: AuNPs bypass endocytosis during their internalization into cells and cytotoxicity of AuNPs. It is also found that both the level of penetration and membrane disruption increase as the charge density of the AuNP increases, but in different manners. The findings suggest a way of controlling the AuNP-cell interactions by manipulating surface charge densities of AuNPs to achieve designated goals in their biomedical applications, such as striking a balance between their cellular uptake and cytotoxicity in order to achieve optimal delivery efficiency as delivery agents.

摘要

纳米颗粒穿透细胞膜是一种有趣的现象,可能对纳米颗粒的生物医学应用有至关重要的影响。在本文中,我们开发了一种金纳米颗粒(AuNPs)的粗粒化模型(通过与现有实验数据进行验证),以模拟它们与模型脂质膜的相互作用。模拟结果表明,具有不同表面电荷符号和密度的 AuNPs 会自发地粘附在双层膜表面或穿透双层膜内部。平均力势能计算表明,粘附或穿透时的能量增益是显著的。在穿透的情况下,发现整个双层膜上叶的缺陷区域被诱导形成,并且形成了一个亲水的孔,水分子可以通过该孔运输,其周围的脂质高度无序。穿透及其伴随的膜破坏可能是实验中观察到的两种现象的一种可能机制:AuNPs 在进入细胞时绕过内吞作用,以及 AuNPs 的细胞毒性。研究还发现,随着 AuNP 表面电荷密度的增加,穿透程度和膜破坏程度都会增加,但方式不同。这些发现为通过操纵 AuNP 的表面电荷密度来控制 AuNP-细胞相互作用提供了一种方法,从而可以在生物医学应用中实现特定的目标,例如在细胞摄取和细胞毒性之间取得平衡,以实现作为递送剂的最佳递送效率。

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