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本文引用的文献

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Lipid-protein nanodiscs as reference medium in detergent screening for high-resolution NMR studies of integral membrane proteins.脂质-蛋白纳米盘作为参考介质在去污剂筛选中的应用,用于高分辨率 NMR 研究整合膜蛋白。
J Am Chem Soc. 2010 Apr 28;132(16):5628-9. doi: 10.1021/ja9097498.
2
Complex formation and light activation in membrane-embedded sensory rhodopsin II as seen by solid-state NMR spectroscopy.固态 NMR 光谱学所见的膜嵌入感受态视紫红质 II 的复合物形成和光激活。
Structure. 2010 Mar 10;18(3):293-300. doi: 10.1016/j.str.2010.01.011.
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Production of multi-subunit complexes on liposome through an E. coli cell-free expression system.通过大肠杆菌无细胞表达系统在脂质体上生产多亚基复合物。
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Recent Advances in the Application of Solution NMR Spectroscopy to Multi-Span Integral Membrane Proteins.溶液核磁共振波谱在多跨膜整合蛋白应用中的最新进展
Prog Nucl Magn Reson Spectrosc. 2009 Nov 1;55(4):335-360. doi: 10.1016/j.pnmrs.2009.07.002.
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Reverse micelle encapsulation of membrane-anchored proteins for solution NMR studies.反胶束包埋法用于膜结合蛋白的溶液 NMR 研究。
Structure. 2010 Jan 13;18(1):9-16. doi: 10.1016/j.str.2009.11.010.
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Three-dimensional structure of the anthrax toxin pore inserted into lipid nanodiscs and lipid vesicles.炭疽毒素孔在脂质纳米盘和脂质囊泡中的三维结构。
Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3453-7. doi: 10.1073/pnas.1000100107. Epub 2010 Feb 8.
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The native conformation of the human VDAC1 N terminus.人电压依赖性阴离子通道1(VDAC1)N端的天然构象。
Angew Chem Int Ed Engl. 2010 Mar 1;49(10):1882-5. doi: 10.1002/anie.200906241.
8
Structure of the amantadine binding site of influenza M2 proton channels in lipid bilayers.流感 M2 质子通道在脂质双层中的金刚烷胺结合位点的结构。
Nature. 2010 Feb 4;463(7281):689-92. doi: 10.1038/nature08722.
9
Amphipols and fluorinated surfactants: Two alternatives to detergents for studying membrane proteins in vitro.两性离子聚合物和氟化表面活性剂:用于体外研究膜蛋白的两种替代去污剂的物质。
Methods Mol Biol. 2010;601:219-45. doi: 10.1007/978-1-60761-344-2_14.
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Practical considerations of membrane protein instability during purification and crystallisation.膜蛋白在纯化和结晶过程中稳定性的实际考量
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非胶束体系用于膜蛋白的溶液核磁共振波谱学研究。

Nonmicellar systems for solution NMR spectroscopy of membrane proteins.

机构信息

Harvard Medical School, Boston, MA 02115, USA.

出版信息

Curr Opin Struct Biol. 2010 Aug;20(4):471-9. doi: 10.1016/j.sbi.2010.05.006.

DOI:10.1016/j.sbi.2010.05.006
PMID:20570504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2928847/
Abstract

Integral membrane proteins play essential roles in many biological processes, such as energy transduction, transport of molecules, and signaling. The correct function of membrane proteins is likely to depend strongly on the chemical and physical properties of the membrane. However, membrane proteins are not accessible to many biophysical methods in their native cellular membrane. A major limitation for their functional and structural characterization is thus the requirement for an artificial environment that mimics the native membrane to preserve the integrity and stability of the membrane protein. Most commonly employed are detergent micelles, which can however be detrimental to membrane protein activity and stability. Here, we review recent developments for alternative, nonmicellar solubilization techniques, with a particular focus on their application to solution NMR studies. We discuss the use of amphipols and lipid bilayer systems, such as bicelles and nanolipoprotein particles (NLPs). The latter show great promise for structural studies in near native membranes.

摘要

整合膜蛋白在许多生物过程中发挥着重要作用,例如能量转导、分子运输和信号转导。膜蛋白的正确功能很可能强烈依赖于膜的化学和物理性质。然而,在其天然细胞膜中,许多生物物理方法无法接触到膜蛋白。因此,它们的功能和结构表征的主要限制是需要一种模拟天然膜的人工环境来保持膜蛋白的完整性和稳定性。最常用的是去污剂胶束,但它们可能对膜蛋白的活性和稳定性有害。在这里,我们综述了替代非胶束溶解技术的最新进展,特别关注它们在溶液 NMR 研究中的应用。我们讨论了使用 Amphipols 和脂质双层系统,如双脂体和纳米脂蛋白颗粒 (NLPs)。后者在近天然膜的结构研究中显示出巨大的潜力。