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内源性大麻素配体花生四烯乙醇胺在膜双分子层中的构象、位置及动态特性。

The conformation, location, and dynamic properties of the endocannabinoid ligand anandamide in a membrane bilayer.

作者信息

Tian Xiaoyu, Guo Jianxin, Yao Fenmei, Yang De-Ping, Makriyannis Alexandros

机构信息

Center for Drug Discovery, Northeastern University, Boston, Massachusetts 02115, USA.

出版信息

J Biol Chem. 2005 Aug 19;280(33):29788-95. doi: 10.1074/jbc.M502925200. Epub 2005 Jun 17.

Abstract

The endogenous cannabinoid ligand anandamide is biosynthesized from membrane phospholipid precursors and is believed to reach its sites of action on the CB1 and CB2 receptors through fast lateral diffusion within the cell membrane. To gain a better insight on the stereochemical features of its association with the cell membrane and its interaction with the cannabinoid receptors, we have studied its conformation, location, and dynamic properties in a dipalmitoylphosphatidylcholine multilamellar model membrane bilayer system. By exploiting the bilayer lattice as an internal three-dimensional reference grid, the conformation and location of anandamide were determined by measuring selected inter- and intramolecular distances between strategically introduced isotopic labels using the rotational echo double resonance (REDOR) NMR method. A molecular model was proposed to represent the structural features of our anandamide/lipid system and was subsequently used in calculating the multispin dephasing curves. Our results demonstrate that anandamide adopts an extended conformation within the membrane with its headgroup at the level of the phospholipid polar group and its terminal methyl group near the bilayer center. Parallel static (2)H NMR experiments further confirmed these findings and provided evidence that anandamide experiences dynamic properties similar to those of the membrane phospholipids and produces no perturbation to the bilayer. Our results are congruent with a hypothesis that anandamide approaches its binding site by laterally diffusing within one membrane leaflet in an extended conformation and interacts with a hydrophobic groove formed by helices 3 and 6 of CB1, where its terminal carbon is positioned close to a key cysteine residue in helix 6 leading to receptor activation.

摘要

内源性大麻素配体花生四烯乙醇胺由膜磷脂前体生物合成,据信它通过在细胞膜内的快速横向扩散到达其在CB1和CB2受体上的作用位点。为了更好地了解其与细胞膜结合的立体化学特征及其与大麻素受体的相互作用,我们在二棕榈酰磷脂酰胆碱多层模型膜双层系统中研究了它的构象、位置和动态特性。通过将双层晶格用作内部三维参考网格,利用旋转回波双共振(REDOR)核磁共振方法测量策略性引入的同位素标记之间选定的分子间和分子内距离,确定了花生四烯乙醇胺的构象和位置。提出了一个分子模型来表示我们的花生四烯乙醇胺/脂质系统的结构特征,随后用于计算多自旋去相位曲线。我们的结果表明,花生四烯乙醇胺在膜内呈伸展构象,其头部基团位于磷脂极性基团水平,其末端甲基靠近双层中心。平行静态(2)H核磁共振实验进一步证实了这些发现,并提供了证据表明花生四烯乙醇胺具有与膜磷脂相似的动态特性,且不会对双层产生扰动。我们的结果与一个假设一致,即花生四烯乙醇胺以伸展构象在一个膜小叶内横向扩散接近其结合位点,并与CB1的螺旋3和6形成的疏水凹槽相互作用,其末端碳靠近螺旋6中的一个关键半胱氨酸残基导致受体激活。

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