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本文引用的文献

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The structure of Bcl-w reveals a role for the C-terminal residues in modulating biological activity.Bcl-w的结构揭示了C末端残基在调节生物活性方面的作用。
EMBO J. 2003 Apr 1;22(7):1497-507. doi: 10.1093/emboj/cdg144.
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Hydration-optimized oriented phospholipid bilayer samples for solid-state NMR structural studies of membrane proteins.用于膜蛋白固态核磁共振结构研究的水合优化取向磷脂双分子层样品。
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Solution structure of human BCL-w: modulation of ligand binding by the C-terminal helix.人源 BCL-w 的溶液结构:C 端螺旋对配体结合的调控
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Simultaneous assignment and structure determination of a membrane protein from NMR orientational restraints.基于核磁共振取向限制同时确定膜蛋白的归属和结构
Protein Sci. 2003 Mar;12(3):403-11. doi: 10.1110/ps.0211503.
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Expression and characterization of the FXYD ion transport regulators for NMR structural studies in lipid micelles and lipid bilayers.用于脂质微团和脂质双层中核磁共振结构研究的FXYD离子转运调节蛋白的表达与特性分析
Biochim Biophys Acta. 2003 Jan 31;1645(1):15-21. doi: 10.1016/s1570-9639(02)00473-9.
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Using pisa pies to resolve ambiguities in angular constraints from PISEMA spectra of aligned proteins.利用比萨饼图解决来自对齐蛋白质的PISEMA光谱中角度限制的模糊性问题。
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7
Phospholemman (FXYD1) associates with Na,K-ATPase and regulates its transport properties.磷膜蛋白(FXYD1)与钠钾ATP酶结合并调节其转运特性。
Proc Natl Acad Sci U S A. 2002 Aug 20;99(17):11476-81. doi: 10.1073/pnas.182267299. Epub 2002 Aug 8.
8
FXYD7 is a brain-specific regulator of Na,K-ATPase alpha 1-beta isozymes.FXYD7是钠钾ATP酶α1-β同工酶的脑特异性调节因子。
EMBO J. 2002 Jul 1;21(13):3264-73. doi: 10.1093/emboj/cdf330.
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Solution structure of a Bcl-2 homolog from Kaposi sarcoma virus.卡波西肉瘤病毒中一种Bcl-2同源物的溶液结构。
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Differential regulation of renal Na,K-ATPase by splice variants of the gamma subunit.γ亚基剪接变体对肾钠钾ATP酶的差异调节
J Biol Chem. 2002 Mar 22;277(12):10162-72. doi: 10.1074/jbc.M111552200. Epub 2001 Dec 27.

膜中凋亡及离子转运调节蛋白的结构研究

Structural studies of apoptosis and ion transport regulatory proteins in membranes.

作者信息

Franzin Carla M, Choi Jungyuen, Zhai Dayong, Reed John C, Marassi Francesca M

机构信息

The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Magn Reson Chem. 2004 Feb;42(2):172-9. doi: 10.1002/mrc.1322.

DOI:10.1002/mrc.1322
PMID:14745797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3033199/
Abstract

Solid-state NMR spectroscopy is being used to determine the structures of membrane proteins involved in the regulation of apoptosis and ion transport. The Bcl-2 family includes pro- and anti-apoptotic proteins that play a major regulatory role in mitochondrion-dependent apoptosis or programmed cell death. The NMR data obtained for (15)N-labeled anti-apoptotic Bcl-xL in lipid bilayers are consistent with membrane association through insertion of the two central hydrophobic alpha-helices that are also required for channel formation and cytoprotective activity. The FXYD family proteins regulate ion flux across membranes, through interaction with the Na(+), K(+)-ATPase, in tissues that perform fluid and solute transport or that are electrically excitable. We have expressed and purified three FXYD family members, Mat8 (mammary tumor protein), CHIF (channel-inducing factor) and PLM (phospholemman), for structure determination by NMR in lipids. The solid-state NMR spectra of Bcl-2 and FXYD proteins, in uniaxially oriented lipid bilayers, give the first view of their membrane-associated architectures.

摘要

固态核磁共振光谱法正被用于确定参与细胞凋亡调节和离子转运的膜蛋白结构。Bcl-2家族包括促凋亡蛋白和抗凋亡蛋白,它们在依赖线粒体的细胞凋亡或程序性细胞死亡中起主要调节作用。在脂质双层中获得的针对(15)N标记的抗凋亡蛋白Bcl-xL的核磁共振数据与通过插入两个中央疏水α螺旋与膜结合一致,这两个螺旋也是通道形成和细胞保护活性所必需的。FXYD家族蛋白通过与Na(+)、K(+)-ATP酶相互作用,在进行液体和溶质转运或具有电兴奋性的组织中调节跨膜离子通量。我们已经表达并纯化了三个FXYD家族成员,Mat8(乳腺肿瘤蛋白)、CHIF(通道诱导因子)和PLM(磷膜蛋白),用于通过脂质中的核磁共振确定结构。在单轴取向脂质双层中,Bcl-2和FXYD蛋白的固态核磁共振光谱首次展示了它们与膜相关的结构。