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一种量化薄溶剂化聚合物膜内分子扩散的方法:以天然展开核孔蛋白膜为例。

A Method to Quantify Molecular Diffusion within Thin Solvated Polymer Films: A Case Study on Films of Natively Unfolded Nucleoporins.

机构信息

School of Biomedical Sciences, Faculty of Biological Sciences, School of Physics and Astronomy, Faculty of Engineering and Physical Sciences, Astbury Centre of Structural Molecular Biology, and Bragg Centre for Materials Research, University of Leeds, Leeds, LS2 9JT, United Kingdom.

University Grenoble Alpes, CNRS, LIPhy, 38000 Grenoble, France.

出版信息

ACS Nano. 2020 Aug 25;14(8):9938-9952. doi: 10.1021/acsnano.0c02895. Epub 2020 Jul 22.

Abstract

We present a method to probe molecular and nanoparticle diffusion within thin, solvated polymer coatings. The device exploits the confinement with well-defined geometry that forms at the interface between a planar and a hemispherical surface (of which at least one is coated with polymers) in close contact and uses this confinement to analyze diffusion processes without interference of exchange with and diffusion in the bulk solution. With this method, which we call plane-sphere confinement microscopy (PSCM), information regarding the partitioning of molecules between the polymer coating and the bulk liquid is also obtained. Thanks to the shape of the confined geometry, diffusion and partitioning can be mapped as a function of compression and concentration of the coating in a single experiment. The method is versatile and can be integrated with conventional optical microscopes; thus it should find widespread use in the many application areas exploiting functional polymer coatings. We demonstrate the use of PSCM using brushes of natively unfolded nucleoporin domains rich in phenylalanine-glycine repeats (FG domains). A meshwork of FG domains is known to be responsible for the selective transport of nuclear transport receptors (NTRs) and their macromolecular cargos across the nuclear envelope that separates the cytosol and the nucleus of living cells. We find that the selectivity of NTR uptake by FG domain films depends sensitively on FG domain concentration and that the interaction of NTRs with FG domains obstructs NTR movement only moderately. These observations contribute important information to better understand the mechanisms of selective NTR transport.

摘要

我们提出了一种探测薄的溶剂化聚合物涂层内分子和纳米粒子扩散的方法。该设备利用在紧密接触的平面和半球形表面(至少有一个涂有聚合物)之间形成的具有明确定义几何形状的限制来分析扩散过程,而不会受到与本体溶液交换和扩散的干扰。我们将这种方法称为平面-半球限制显微镜(PSCM),还可以获得有关分子在聚合物涂层和本体液体之间分配的信息。由于受限几何形状的形状,扩散和分配可以在单个实验中作为涂层压缩和浓度的函数进行映射。该方法具有通用性,可以与传统的光学显微镜集成;因此,它应该在利用功能聚合物涂层的许多应用领域中得到广泛应用。我们使用富含苯丙氨酸-甘氨酸重复序列(FG 结构域)的天然展开核孔蛋白域的刷来演示 PSCM 的用途。众所周知,FG 结构域的网状结构负责选择性地将核转运受体(NTR)及其大分子货物穿过核膜运输,核膜将细胞质和活细胞的细胞核分隔开。我们发现,FG 域薄膜对 NTR 的摄取选择性对 FG 域浓度非常敏感,并且 NTR 与 FG 域的相互作用仅适度阻碍 NTR 的运动。这些观察结果为更好地理解选择性 NTR 运输的机制提供了重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0159/7526988/014216f15a34/nn0c02895_0001.jpg

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