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Molecular Orientation Determination in Nanodiscs at the Single Molecule Level

机译:单分子水平纳米乳汁中的分子取向测定

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The function of membrane-bound proteins often depends on their interactions with the lipid bilayer. Bulk absorption-based linear dichroism has been historically used to investigate molecular orientations in the phospholipid bilayer but cannot resolve the actual distribution of molecules embedded in the membrane and is often limited by a poor signal-to-noise ratio. Here, we present single-molecule orientation determination by fluorescence-detected linear dichroism visualization in Nanodisc grids or SOLVING, to determine the molecular orientation of molecules assembled into nanoscale lipid bilayers. We provide a proof-of-concept by using SOLVING to quantitate the orientation distribution of two commonly used fluorescent dyes, DiO and BODIPY, in 10 nm Nanodiscs. Besides confirming the mean orientation determined by bulk absorption measurement, SOLVING provides the actual distribution of orientations and promises to provide key molecular insights into the topology and interactions of multiprotein complexes, such as those observed in intracellular signal transduction.
机译:膜结合蛋白的功能通常取决于它们与脂质双层的相互作用。散装吸收的线性二色性历史上用于研究磷脂双层中的分子取向,但不能解析嵌入膜中的分子的实际分布,并且通常受到不良信噪比的限制。这里,我们通过纳米型栅格或求解的荧光检测的线性二色性可视化呈现单分子取向测定,以确定组装成纳米级脂质双层分子的分子取向。我们通过使用求解定量两种常用的荧光染料,DIO和BODIPY的定向分布,提供概念证据。除了确认通过散装吸收测量确定的平均方向之外,求解提供了方向的实际分布,并承诺为多粒蛋白复合物的拓扑和相互作用提供关键的分子见解,例如在细胞内信号转导中观察到的那些。

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