CUBIC MEMBRANES: THE MISSING DIMENSION OF CELL MEMBRANE ORGANIZATION

被引:116
作者
Almsherqi, Zakaria A. [1 ]
Landh, Tomas [2 ]
Kohlwein, Sepp D. [3 ]
Deng, Yuru [1 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore 117597, Singapore
[2] Novo Nordisk AS, DK-2760 Malov, Denmark
[3] Graz Univ, Inst Mol Biosci, A-8010 Graz, Austria
来源
INTERNATIONAL REVIEW OF CELL AND MOLECULAR BIOLOGY, VOL 274 | 2009年 / 274卷
基金
奥地利科学基金会;
关键词
CRYSTALLOID ENDOPLASMIC-RETICULUM; CONTRACTILE VACUOLE COMPLEX; PROPLASTIDEN ETIOLIERTER BOHNEN; COENZYME-A REDUCTASE; HMG-COA REDUCTASE; MONOOLEIN/DIOLEOYLPHOSPHATIDIC ACID MIXTURES; ROUGH MUTANT LIPOPOLYSACCHARIDE; DES ANNELIDES POLYNOINAE; AMEBA CHAOS-CAROLINENSIS; NOVIKOFF HEPATOMA CELLS;
D O I
10.1016/S1937-6448(08)02006-6
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
Biological membranes are among the most fascinating assemblies of biomolecules: a bilayer less than 10 nm thick, composed of rather small lipid molecules that are held together simply by noncovalent forces, defines the cell and discriminates between "inside" and "outside", survival, and death. Intracellular compartmentalization-governed by biomembranes as well-is a characteristic feature of eukaryotic cells, which allows them to fulfill multiple and highly specialized anabolic and catabolic functions in strictly controlled environments. Although cellular membranes are generally visualized as flat sheets or closely folded isolated objects, multiple observations also demonstrate that membranes may fold into "unusual", highly organized structures with 2D or 3D periodicity. The obvious correlation of highly convoluted membrane organizations with pathological cellular states, for example, as a consequence of viral infection, deserves close consideration. However, knowledge about formation and function of these highly organized 3D periodic membrane structures is scarce, primarily due to the tack of appropriate techniques for their analysis in vivo. Currently, the only direct way to characterize cellular membrane architecture is by transmission electron microscopy (TEM). However, deciphering the spatial architecture solely based on two-dimensionally projected TEM images is a challenging task and prone to artifacts. In this review, we wilt provide an update on the current progress in identifying and analyzing 3D membrane architectures in biological systems, with a special focus on membranes with cubic symmetry, and their potential role in physiological and pathophysiological conditions. Proteomics and lipidomics approaches in defined experimental cell systems may prove instrumental to understand formation and function of 3D membrane morphologies.
引用
收藏
页码:275 / 342
页数:68
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