Diversity and versatility of lipid-protein interactions revealed by molecular genetic approaches

被引:107
作者
Dowhan, W [1 ]
Mileykovskaya, E [1 ]
Bogdanov, M [1 ]
机构
[1] Univ Texas, Sch Med, Dept Biochem & Mol Biol, Houston, TX 77030 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2004年 / 1666卷 / 1-2期
关键词
amphitropic protein; protein topology; phospholipid; cell division; lipid domain; DNA replication; lipochaperone; protein folding; membrane;
D O I
10.1016/j.bbamem.2004.04.010
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
dThe diversity in structures and physical properties of lipids provides a wide variety of possible interactions with proteins that affect their assembly, organization, and function either at the surface of or within membranes. Because lipids have no catalytic activity, it has been challenging to define many of their precise functions in vivo in molecular terms. Those processes responsive to lipids are attuned to the native lipid environment for optimal function, but evidence that lipids with similar properties or even detergents can sometimes partially replace the natural lipid environment has led to uncertainty as to the requirement for specific lipids. The development of strains of microorganisms in which membrane lipid composition can be genetically manipulated in viable cells has provided a set of reagents to probe lipid functions. These mutants have uncovered previously unrecognized roles for lipids and provided in vivo verification for putative functions described in vitro. In this review, we summarize how these reagent strains have provided new insight into the function of lipids. The role of specific lipids in membrane protein folding and topological organization is reviewed. The evidence is summarized for the involvement of anionic lipidenriched domains in the organization of amphitropic proteins on the membrane surface into molecular machines involved in DNA replication and cell division. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 39
页数:21
相关论文
共 180 条
[1]   Structure and mechanism of the lactose permease of Escherichia coli [J].
Abramson, J ;
Smirnova, I ;
Kasho, V ;
Verner, G ;
Kaback, HR ;
Iwata, S .
SCIENCE, 2003, 301 (5633) :610-615
[2]   MINIATURE ESCHERICHIA COLI CELLS DEFICIENT IN DNA [J].
ADLER, HI ;
FISHER, WD ;
COHEN, A ;
HARDIGREE, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 57 (02) :321-+
[3]   CELL-DIVISION IN ESCHERICHIA-COLI MINB MUTANTS [J].
AKERLUND, T ;
BERNANDER, R ;
NORDSTROM, K .
MOLECULAR MICROBIOLOGY, 1992, 6 (15) :2073-2083
[5]   INVIVO EXPRESSION OF THE LACY GENE IN 2 SEGMENTS LEADS TO FUNCTIONAL LAC PERMEASE [J].
BIBI, E ;
KABACK, HR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4325-4329
[6]   A polytopic membrane protein displays a reversible topology dependent on membrane lipid composition [J].
Bogdanov, M ;
Heacock, PN ;
Dowhan, W .
EMBO JOURNAL, 2002, 21 (09) :2107-2116
[7]   Lipid-assisted protein folding [J].
Bogdanov, M ;
Dowhan, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) :36827-36830
[8]   Phospholipid-assisted protein folding: phosphatidylethanolamine is required at a late step of the conformational maturation of the polytopic membrane protein lactose permease [J].
Bogdanov, M ;
Dowhan, W .
EMBO JOURNAL, 1998, 17 (18) :5255-5264
[9]   Phospholipid-assisted refolding of an integral membrane protein - Minimum structural features for phosphatidylethanolamine to act as a molecular chaperone [J].
Bogdanov, M ;
Umeda, M ;
Dowhan, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12339-12345
[10]   A phospholipid acts as a chaperone in assembly of a membrane transport protein [J].
Bogdanov, M ;
Sun, JZ ;
Kaback, HR ;
Dowhan, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (20) :11615-11618