The Role of Phosphatidic Acid and Cardiolipin in Stability of the Tetrameric Assembly of Potassium Channel KcsA

被引:22
|
作者
Raja, Mobeen [1 ,2 ]
机构
[1] Univ Alberta, Alberta Diabet Inst, Sch Mol & Syst Med, Edmonton, AB T6G 2E1, Canada
[2] Univ Utrecht, Dept Biochem Membranes, Ctr Biomembranes & Lipid Enzymol, Inst Biomembranes, NL-3584 CH Utrecht, Netherlands
来源
JOURNAL OF MEMBRANE BIOLOGY | 2010年 / 234卷 / 03期
关键词
Potassium channel KcsA; Tetrameric stability; Anionic lipids; Phosphatidic acid; Cardiolipin; N-terminus; Electrostatic interactions; Protein-lipid interaction; MOLECULAR-BASIS; RESPIRATORY-CHAIN; K+ CHANNEL; MEMBRANE; PROTEIN; LIPIDS; DEHYDROGENASE; MITOCHONDRIA; ARCHITECTURE; GENERATION;
D O I
10.1007/s00232-010-9251-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, the roles of two anionic phospholipids-phosphatidic acid (PA), which is an important signaling molecule, and cardiolipin (CL), which plays a crucial role in the bioenergetics of the cell-in stabilizing the oligomeric structure of potassium channel KcsA were determined. The stability of KcsA was drastically increased as a function of PA or CL content (mol%) in phosphatidylcholine (PC) bilayers. Deletion of the membrane-associated N terminus significantly reduced channel stability at high levels of PA content; however, the intrinsic stability of this protein was marginally affected in the presence of CL. These studies indicate that the electrostatic-hydrogen bond switch between PA and N terminus, involving basic residues, is much stronger than the stabilizing effect of CL. Furthermore, the unique properties of the PA headgroup alter protein assembly and folding properties differently from the CL headgroup, and both lipids stabilize the tetrameric assembly via their specific interaction on the extra- or the intracellular side of KcsA.
引用
收藏
页码:235 / 240
页数:6
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