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Dash-and-Recruit Mechanism Drives Membrane Curvature Recognition by the Small Bacterial Protein SpoVM.Dash-and-Recruit 机制驱动小型细菌蛋白 SpoVM 识别膜曲率。
Cell Syst. 2017 Nov 22;5(5):518-526.e3. doi: 10.1016/j.cels.2017.10.004. Epub 2017 Nov 1.
3
Microfluidics for exosome isolation and analysis: enabling liquid biopsy for personalized medicine.微流控技术用于外泌体的分离和分析:为个性化医疗提供液体活检。
Lab Chip. 2017 Oct 25;17(21):3558-3577. doi: 10.1039/c7lc00592j.
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Effect of Size and Surface Charge of Gold Nanoparticles on their Skin Permeability: A Molecular Dynamics Study.金纳米粒子的尺寸和表面电荷对其皮肤渗透性的影响:分子动力学研究。
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5
The Ins and Outs of Lipid Flip-Flop.脂双层翻转的来龙去脉。
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Direct proof of spontaneous translocation of lipid-covered hydrophobic nanoparticles through a phospholipid bilayer.直接证明了带脂质覆盖的疏水分子纳米颗粒通过磷脂双层的自发转运。
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Lipid Vesicle Interaction with Hydrophobic Surfaces: A Coarse-Grained Molecular Dynamics Study.脂双层与疏水表面的相互作用:粗粒化分子动力学研究。
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Surface-enhanced Raman scattering measurement from a lipid bilayer encapsulating a single decahedral nanoparticle mediated by an optical trap.脂质双层内单十面体纳米颗粒的表面增强拉曼散射测量,由光阱介导。
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10
Molecular Dynamics Studies of Liposomes as Carriers for Photosensitizing Drugs: Development, Validation, and Simulations with a Coarse-Grained Model.脂质体作为光敏药物载体的分子动力学研究:粗粒度模型的开发、验证及模拟
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纳米囊泡与纳米颗粒支撑脂质双层:双层结构以及脂质分子和纳米受限水中的扩散率存在巨大差异。

Nanovesicles Versus Nanoparticle-Supported Lipid Bilayers: Massive Differences in Bilayer Structures and in Diffusivities of Lipid Molecules and Nanoconfined Water.

机构信息

Department of Mechanical Engineering , University of Maryland , College Park , Maryland 20742 , United States.

Laboratory of Molecular Biology , National Cancer Institute, National Institutes of Health , Bethesda , Maryland 20892 , United States.

出版信息

Langmuir. 2019 Feb 19;35(7):2702-2708. doi: 10.1021/acs.langmuir.8b03805. Epub 2019 Feb 11.

DOI:10.1021/acs.langmuir.8b03805
PMID:30685976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7464572/
Abstract

We carry out molecular dynamics (MD) simulations to compare the equilibrium architecture and properties of nanoparticle-supported lipid bilayers (NPSLBLs) with the free vesicles of similar dimensions. Three key differences emerge. First, we witness that for a free vesicle, a much larger number of lipid molecules occupy the outer layer as compared to the inner layer; on the other hand, for the NPSLBL the number of lipid molecules occupying the inner and outer layers is identical. Second, we witness that the diffusivities of the lipid molecules occupying both the inner and the outer layers of the free vesicles are identical, whereas for the NPSLBLs the diffusivity of the lipid molecules in the outer layer is more than twice the diffusivity of the lipid molecules in the inner layer. Finally, the NPSLBLs entrap nanoscopic thin water film between the inner lipid layer and the NP and the diffusivity of this water film is nearly 1 order of magnitude smaller than the diffusivity of the bulk water; on the other hand, the water inside the free vesicles has a diffusivity that is only slightly lower than that of the bulk water. Our findings, possibly the first probing the atomistic details of the NPSLBLs, are anticipated to shed light on the properties of this important nanomaterial with applications in a large number of disciplines ranging from drug and gene delivery to characterizing curvature-sensitive molecules.

摘要

我们进行了分子动力学(MD)模拟,以比较具有相似尺寸的纳米颗粒支撑脂质双层(NPSLBL)与游离囊泡的平衡结构和性质。有三个关键区别。首先,我们发现对于自由囊泡,与内层相比,更多的脂质分子占据外层;另一方面,对于 NPSLBL,占据内层和外层的脂质分子数量相同。其次,我们发现占据自由囊泡内层和外层的脂质分子的扩散率是相同的,而对于 NPSLBL,外层的脂质分子的扩散率是内层的两倍多。最后,NPSLBL 在内层脂质层和 NP 之间捕获纳米级薄的水膜,并且该水膜的扩散率比体相水的扩散率小近一个数量级;另一方面,自由囊泡内的水的扩散率仅略低于体相水。我们的发现,可能是首次探测 NPSLBL 的原子细节,有望阐明这种具有广泛应用的重要纳米材料的性质,从药物和基因传递到表征对曲率敏感的分子。