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Curvature-mediated cooperative wrapping of multiple nanoparticles at the same and opposite membrane sides

机译:Curvature-mediated合作包装多个纳米颗粒相同,方向相反膜两侧

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摘要

Cell membrane interactions with nanoparticles (NPs) are essential to cellular functioning and mostly accompanied by membrane curvature generation and sensing. Multiple NPs inducing curvature from one side of a membrane are believed to be wrapped cooperatively by the membrane through curvature-mediated interactions. However, little is known about another biologically ubiquitous and important case, i.e., NPs binding to opposite membrane sides induce a curved bend of different directions. Combining coarse-grained molecular dynamics and theoretical analysis, here we systematically investigate the cooperative effect in the wrapping of multiple adhesive NPs at the same and opposite membrane sides and demonstrate the importance of the magnitude and direction of the membrane bend in regulating curvature-mediated NP interactions. Effects of the NP size, size difference, initial distance, number, and strength of adhesion with the membrane on the wrapping cooperativity and wrapping states are analyzed. For NPs binding to the same membrane side, rich membrane wrapping and NP aggregation states are observed, and the curvature-mediated interactions could be either attractive or repulsive, depending on the initial NP distance and the competition between the membrane bending, NP binding and membrane protrusion. In sharp contrast, the interaction between two NPs binding to opposite membrane sides is always attractive and the cooperative wrapping of NPs is promoted, as the curved membrane regions induced by the NPs are shared in a manner that the NP-membrane contact is increased and the energy cost of membrane bending is reduced. Owing to the ubiquity and heterogeneity of membrane shaping proteins in biology, our results enrich the cutting-edge knowledge on the curvature-mediated interaction of NPs for better and profound understanding on high-order cooperative assemblies of NPs or proteins in numerous biological processes.
机译:细胞膜与纳米粒子的相互作用(NPs)对细胞功能和至关重要主要是伴随着膜曲率代和遥感。从膜的一侧弯曲认为是合作的膜通过curvature-mediated交互。然而,另一个是知之甚少生物无处不在的和重要的情况下,也就是说,NPs绑定到相反的膜诱导不同的方向的弯曲的弯曲。粗粒度的分子动力学和理论分析,我们系统地研究在包装多个合作效果粘结剂NPs相同和相反的膜两边和演示的重要性膜的大小和方向弯曲调节curvature-mediated NP交互。NP的影响大小,大小不同,初始距离、数量和力量的附着力包装上的膜协同包装状态进行了分析。相同的膜方面,丰富的膜包装和NP聚合状态观察可以是curvature-mediated交互根据最初的吸引或排斥NP距离之间的竞争膜弯曲,NP绑定和膜突出。两个NPs绑定到相反的膜总是有吸引力的和合作包装NPs提拔,弯曲膜区域诱导NPs是共享的NP-membrane接触的方式能源成本的增加,膜弯曲减少了。膜形成蛋白质的异质性生物学,我们的研究结果丰富了尖端知识在curvature-mediated交互NPs更好的和深刻的理解高阶合作NPs或组件蛋白质在许多生物过程。

著录项

  • 来源
    《Nanoscale》 |2019年第42期|19751-19762|共12页
  • 作者单位

    Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China;

    China Univ Petr East China, Coll Chem Engn, Ctr Bioengn & Biotechnol, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China;

    Peking Univ, Coll Engn, Beijing Innovat Ctr Engn Sci & Adv Technol, Dept Mech & Engn Sci, Beijing 100871, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 英语
  • 中图分类 Online;
  • 关键词

    Energy costs; Wrapping; SynergismmembraneBond strength(Materials)NPsidings;

    机译:能源成本;包装;SynergismmembraneBond(材料)NPsidings力量;

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