The role of nonbilayer phospholipids in mitochondrial structure and function

被引:114
作者
Ball, Writoban Basu [1 ]
Neff, John K. [1 ]
Gohil, Vishal M. [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
基金
美国国家卫生研究院;
关键词
cardiolipin; mitochondria; phosphatidylethanolamine; RESPIRATORY-CHAIN SUPERCOMPLEXES; PHOSPHATIDYLSERINE DECARBOXYLASE 1; YEAST SACCHAROMYCES-CEREVISIAE; ELECTRON-TRANSPORT CHAIN; BARTH-SYNDROME; INNER MEMBRANE; CARDIOLIPIN BIOSYNTHESIS; PHOSPHATIDYLETHANOLAMINE LEVEL; OXIDATIVE-PHOSPHORYLATION; MAMMALIAN MITOCHONDRIA;
D O I
10.1002/1873-3468.12887
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
Mitochondrial structure and function are influenced by the unique phospholipid composition of its membranes. While mitochondria contain all the major classes of phospholipids, recent studies have highlighted specific roles of the nonbilayer-forming phospholipids phosphatidylethanolamine (PE) and cardiolipin (CL) in the assembly and activity of mitochondrial respiratory chain (MRC) complexes. The nonbilayer phospholipids are cone-shaped molecules that introduce curvature stress in the bilayer membrane and have been shown to impact mitochondrial fusion and fission. In addition to their overlapping roles in these mitochondrial processes, each nonbilayer phospholipid also plays a unique role in mitochondrial function; for example, CL is specifically required for MRC supercomplex formation. Recent discoveries of mitochondrial PE- and CL-trafficking proteins and prior knowledge of their biosynthetic pathways have provided targets for precisely manipulating nonbilayer phospholipid levels in the mitochondrial membranes in vivo. Thus, the genetic mutants of these pathways could be valuable tools in illuminating molecular functions and biophysical properties of nonbilayer phospholipids in driving mitochondrial bioenergetics and dynamics.
引用
收藏
页码:1273 / 1290
页数:18
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