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通过顺磁弛豫增强测量双胶束中脂质碳的浸深。

Immersion Depths of Lipid Carbons in Bicelles Measured by Paramagnetic Relaxation Enhancement.

机构信息

Department of Biochemistry and Biophysics, Stockholm University , SE-106 91 Stockholm, Sweden.

出版信息

J Phys Chem B. 2017 Aug 17;121(32):7660-7670. doi: 10.1021/acs.jpcb.7b05822. Epub 2017 Aug 2.

Abstract

Myriads of biological processes occur in or at cellular lipid membranes. Knowledge about the localization of proteins, lipids, and other molecules within biological membranes is thus crucial for the understanding of such processes. Here, we present a method to determine the immersion depths of lipid carbon atoms in membranes by paramagnetic relaxation enhancement (PRE) caused by the presence of doxylated lipids. As membrane mimetics, we employ small isotropic bicelles made of synthetic lipids and of natural Escherichia coli phospholipid extract. Bicelles are particularly suitable for solution state NMR since they maintain a lipid bilayer while they are at the same time amenable to solution state NMR experiments. PREs were measured in the presence of different doxylated lipids with the nitroxide radical located in the headgroup and at various positions in the acyl chain. Theoretical PREs were calculated assuming a simple bicelle model using the Solomon-Bloembergen equations. Immersion depths of the lipid carbon atoms were obtained by a least-squares fit of the theoretical to the experimental PREs. The carbon immersion depths correspond well to results obtained by other methods and differences do not exceed 3-5 Å. This means that the method presented here provides sufficient resolution to distinguish the localization of carbons in different regions of the lipid bilayer, despite considerable simplifications of the underlying theory. These simplifications include a simple form of the spectral density function, which we find is sufficient to reliably determine immersion depths. A more complicated spectral density function that includes bicelle, lipid, and local motions may only improve the results if its parametrization is good enough. The approach presented here may be extended to the determination of protein localization in membranes employing realistic membrane mimetics like the bicelles made of E. coli phospholipid extract used here.

摘要

无数的生物过程发生在细胞脂质膜内或表面。因此,了解蛋白质、脂质和其他分子在生物膜内的定位对于理解这些过程至关重要。在这里,我们提出了一种通过存在的 doxylated 脂质引起的顺磁弛豫增强 (PRE) 来确定脂质碳原子在膜内的浸入深度的方法。作为膜模拟物,我们采用由合成脂质和天然大肠杆菌磷脂提取物制成的各向同性小双分子层。双分子层特别适合溶液状态 NMR,因为它们在保持脂质双层的同时,也适用于溶液状态 NMR 实验。在存在不同 doxylated 脂质的情况下测量了 PRE,其中硝氧自由基位于头基和酰链的不同位置。使用 Solomon-Bloembergen 方程,根据简单的双分子层模型计算了理论 PRE。通过将理论 PRE 与实验 PRE 进行最小二乘拟合,获得了脂质碳原子的浸入深度。碳浸入深度与其他方法获得的结果非常吻合,差异不超过 3-5 Å。这意味着,尽管基础理论有相当大的简化,但这里提出的方法提供了足够的分辨率来区分脂质双层不同区域的碳原子定位。这些简化包括谱密度函数的简单形式,我们发现它足以可靠地确定浸入深度。如果包含双分子层、脂质和局部运动的更复杂的谱密度函数的参数化足够好,可能只会改善结果。这里提出的方法可以扩展到使用像这里使用的大肠杆菌磷脂提取物制成的双分子层等实际膜模拟物来确定蛋白质在膜中的定位。

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