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Inducing conformational preference of the membrane protein transporter EmrE through conservative mutations.通过保守突变诱导膜蛋白转运体 EmrE 的构象偏好。
Elife. 2019 Oct 22;8:e48909. doi: 10.7554/eLife.48909.
2
Improving the quality of oriented membrane protein spectra using heat-compensated separated local field experiments.利用热补偿分离局域场实验提高定向膜蛋白谱的质量。
J Biomol NMR. 2019 Nov;73(10-11):617-624. doi: 10.1007/s10858-019-00273-1. Epub 2019 Aug 28.
3
Solid-state NMR spectroscopy based atomistic view of a membrane protein unfolding pathway.基于固态 NMR 光谱的膜蛋白解折叠途径的原子级观点。
Nat Commun. 2019 Aug 27;10(1):3867. doi: 10.1038/s41467-019-11849-8.
4
Magnetic Alignment of Polymer Macro-Nanodiscs Enables Residual-Dipolar-Coupling-Based High-Resolution Structural Studies by NMR Spectroscopy.聚合物宏观纳米盘的磁定向使基于残余偶极耦合的高分辨率结构研究成为可能 通过 NMR 光谱。
Angew Chem Int Ed Engl. 2019 Oct 14;58(42):14925-14928. doi: 10.1002/anie.201907655. Epub 2019 Sep 11.
5
Cholesterol-Dependent Cytolysins: Membrane and Protein Structural Requirements for Pore Formation.胆固醇依赖性细胞溶素:孔形成的膜和蛋白质结构要求。
Chem Rev. 2019 Jul 10;119(13):7721-7736. doi: 10.1021/acs.chemrev.9b00090. Epub 2019 Jun 17.
6
Structures and Interactions of Transmembrane Targets in Native Nanodiscs.天然纳米盘内跨膜靶标结构与相互作用。
SLAS Discov. 2019 Dec;24(10):943-952. doi: 10.1177/2472555219857691. Epub 2019 Jun 26.
7
Solid-State NMR Investigations of the MHC II Transmembrane Domains: Topological Equilibria and Lipid Interactions.固态 NMR 研究 MHC II 跨膜结构域:拓扑平衡和脂质相互作用。
J Membr Biol. 2019 Oct;252(4-5):371-384. doi: 10.1007/s00232-019-00071-8. Epub 2019 Jun 11.
8
Trichogin GA IV Alignment and Oligomerization in Phospholipid Bilayers.发夹菌素 GA IV 在磷脂双层中的排列和寡聚化。
Chembiochem. 2019 Aug 16;20(16):2141-2150. doi: 10.1002/cbic.201900263. Epub 2019 Jul 17.
9
Influence of Mg and Ca on nanodisc formation by diisobutylene/maleic acid (DIBMA) copolymer.镁和钙对二异丁烯/马来酸(DIBMA)共聚物形成纳米盘的影响。
Chem Phys Lipids. 2019 Jul;221:30-38. doi: 10.1016/j.chemphyslip.2019.03.004. Epub 2019 Mar 13.
10
Hydrogen-deuterium exchange mass spectrometry of membrane proteins in lipid nanodiscs.脂质纳米盘中膜蛋白的氢氘交换质谱分析。
Chem Phys Lipids. 2019 May;220:14-22. doi: 10.1016/j.chemphyslip.2019.02.007. Epub 2019 Feb 22.

固态 NMR 光谱法研究聚合物纳米盘的磁性排列。

Magnetic Alignment of Polymer Nanodiscs Probed by Solid-State NMR Spectroscopy.

机构信息

Biophysics Program and Department of Chemistry, Macromolecular Science and Engineering, Biomedical Engineering , University of Michigan , Ann Arbor , Michigan 48109-1055 , United States.

Department of Fine Chemistry , Seoul National University of Science and Technology , Seoul 01811 , Republic of Korea.

出版信息

Langmuir. 2020 Feb 11;36(5):1258-1265. doi: 10.1021/acs.langmuir.9b03538. Epub 2020 Jan 30.

DOI:10.1021/acs.langmuir.9b03538
PMID:31961695
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7414804/
Abstract

The ability of amphipathic polymers to self-assemble with lipids and form nanodiscs has been a boon for the field of functional reconstitution of membrane proteins. In a field dominated by detergent micelles, a unique feature of polymer nanodiscs is their much-desired ability to align in the presence of an external magnetic field. Magnetic alignment facilitates the application of solid-state nuclear magnetic resonance (NMR) spectroscopy and aids in the measurement of residual dipolar couplings via well-established solution NMR spectroscopy. In this study, we comprehensively investigate the magnetic alignment properties of styrene maleimide quaternary ammonium (SMA-QA) polymer-based nanodiscs by using P and N solid-state NMR experiments under static conditions. The results reported herein demonstrate the spontaneous magnetic alignment of large-sized (≥20 nm diameter) SMA-QA nanodiscs (also called as macro-nanodiscs) with the lipid bilayer normal perpendicular to the magnetic field direction. Consequently, the orientation of macro-nanodiscs is further shown to flip the alignment axis parallel to the magnetic field direction upon the addition of a paramagnetic lanthanide salt. These results demonstrate the use of SMA-QA polymer nanodiscs for solid-state NMR applications including structural studies on membrane proteins.

摘要

两亲聚合物与脂质自组装形成纳米盘的能力是膜蛋白功能重建领域的福音。在以胶束为主导的领域中,聚合物纳米盘的一个独特特征是它们在外部磁场存在下能够进行排列,这是人们所期望的。磁定向有助于应用固态核磁共振(NMR)光谱,并通过成熟的溶液 NMR 光谱法辅助测量残磁偶合。在这项研究中,我们通过静态条件下的 P 和 N 固态 NMR 实验,全面研究了基于苯乙烯马来酰亚胺季铵(SMA-QA)聚合物的纳米盘的磁定向性质。本文报道的结果表明,大尺寸(≥20nm 直径)的 SMA-QA 纳米盘(也称为大纳米盘)具有自发的磁定向性,其脂质双层的法向垂直于磁场方向。因此,进一步表明,在添加顺磁镧系盐后,大纳米盘的取向会翻转,使其排列轴与磁场方向平行。这些结果表明 SMA-QA 聚合物纳米盘可用于固态 NMR 应用,包括膜蛋白的结构研究。