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Effect of Receptor Structure and Length on the Wrapping of a Nanoparticle by a Lipid Membrane

机译:受体结构和长度对脂质膜包裹纳米颗粒的影响

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Nanoparticles have been considered as a type of powerful tool to deliver drugs and genes into cells for disease diagnosis and therapies. It has been generally accepted that the internalization of nanoparticles into cells is mostly realized by receptor-mediated endocytosis. However, for the influence of structural factors of receptors on endocytosis, this is still largely unknown. In this paper, computer simulations are applied to investigate the effects of structure (i.e., the number of constituent chains of the receptor) and the length of the receptor on the wrapping behavior of nanoparticles by the lipid membrane, which is a key step of receptor-medicated endocytosis. It is found that these structural factors of receptors have strong effects on the nanoparticle’s final interaction configuration with the membrane in the simulations, such as adhering on the membrane surface or being partly or fully wrapped by the membrane. Furthermore, in some cases, the rupture of the lipid membrane occurs. These results are helpful for the understanding of endocytosis and the preparation of advanced nanoscale drug-delivery vectors.
机译:纳米颗粒被认为是一种将药物和基因传递到细胞中以进行疾病诊断和治疗的强大工具。通常已经接受的是,纳米颗粒内化到细胞中主要是通过受体介导的内吞作用实现的。然而,对于受体的结构因子对内吞作用的影响,仍然很大程度上未知。在本文中,计算机模拟用于研究结构(即受体的组成链数)和受体的长度对脂质膜包裹纳米颗粒包裹行为的影响,这是受体的关键步骤药物内吞作用。在模拟中发现,受体的这些结构因素对纳米粒子与膜的最终相互作用构型有很大影响,例如粘附在膜表面上或被膜部分或完全包裹。此外,在某些情况下,会发生脂质膜破裂。这些结果有助于理解胞吞作用和先进的纳米级药物传递载体的制备。

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