Structural studies of apoptosis and ion transport regulatory proteins in membranes

被引:34
作者
Franzin, CM [1 ]
Choi, JY [1 ]
Zhai, DY [1 ]
Reed, JC [1 ]
Marassi, FM [1 ]
机构
[1] Burnham Inst, La Jolla, CA 92037 USA
关键词
NMR; Bcl-2; Bcl-xL; FXYD; Mat8; PLM; CHIF; apoptosis; membrane proteins; lipid bilayers;
D O I
10.1002/mrc.1322
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 N-15-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. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:172 / 179
页数:8
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