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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.

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。

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