论文标题

一种量化薄溶剂化聚合物膜中分子扩散的方法:一种对本质展开的核苷膜的案例研究

A method to quantify molecular diffusion within thin solvated polymer films: A case study on films of natively unfolded nucleoporins

论文作者

Frost, Rickard, Débarre, Delphine, Jana, Saikat, Bano, Fouzia, Schünemann, Jürgen, Görlich, Dirk, Richter, Ralf P.

论文摘要

我们提出了一种探测分子和纳米颗粒扩散在薄的溶剂化聚合物涂层中的方法。该设备利用与定义明确的几何形状的限制,该几何形状在平面和半球面之间的界面形成(其中至少一个与聚合物覆盖)密切接触,并使用此限制来分析扩散过程,而无需在散装溶液中与交换和扩散的交换干扰。通过这种方法,我们还将获得有关平面球束缚显微镜(PSCM)的信息,还获得了有关分子在聚合物涂层和大量液体之间分配的信息。得益于封闭的几何形状的形状,可以将扩散和分配的映射映射,这是单个实验中涂层的压缩和浓度的函数。该方法具有多功能性,可以与常规光学显微镜集成,因此应该在利用功能性聚合物涂层的许多应用领域中找到广泛的用途。我们证明了使用富含苯丙氨酸 - 甘氨酸重复序列(FG结构域)的本生物展开的核孔蛋白结构域的刷子来证明PSCM的使用。已知FG结构域的网状功能是核转运受体(NTR)及其大分子嘉戈斯的选择性转运,使核包膜分离,将活细胞的细胞质和核分开。我们发现,FG结构域膜对NTR摄取的选择性取决于FG结构域的浓度,并且NTR与FG结构域的相互作用仅妨碍NTR运动。这些观察结果有助于更好地了解选择性NTR传输的机制。

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 hemi-spherical surface (of which at least one is coated with polymers) in close contact, and uses this confinement to analyse 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, and thus 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 (NTR) 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.

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