Red blood cell (RBC) membrane proteomics - Part I: Proteomics and RBC physiology

被引:49
|
作者
Pasini, Erica M. [1 ]
Lutz, Hans U. [2 ]
Mann, Matthias [3 ]
Thomas, Alan W. [1 ]
机构
[1] Biomed Primate Res Ctr, NL-2288 GJ Rijswijk, Netherlands
[2] ETH Honggerberg, Swiss Fed Inst Technol, Inst Biochem, CH-8093 Zurich, Switzerland
[3] Max Planck Inst Biochem, Dept Prote & Signal Transduct, D-82152 Martinsried, Germany
关键词
HUMAN ERYTHROCYTE BAND-3; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; HUMAN GLYCOPHORIN-A; MASS-SPECTROMETRY; PLASMA-MEMBRANE; FUNCTIONAL-CHARACTERIZATION; HEREDITARY SPHEROCYTOSIS; TRANSBILAYER MOVEMENT; MOLECULAR-GENETICS; SKELETAL PROTEINS;
D O I
10.1016/j.jprot.2009.06.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Membrane proteomics is concerned with accurately and sensitively identifying molecules involved in cell compartmentalisation, including those controlling the interface between the cell and the outside world. The high lipid content of the environment in which these proteins are found often causes a particular set of problems that must be overcome when isolating the required material before effective HPLC-MS approaches can be performed. The membrane is an unusually dynamic cellular structure since it interacts with an ever changing environment. A full understanding of this critical cell component will ultimately require, in addition to proteomics, lipidomics, glycomics, interactomics and study of post-translational modifications. Devoid of nucleus and organelles in mammalian species other than camelids, and constantly in motion in the blood stream, red blood cells (RBCs) are the sole mammalian oxygen transporter. The fact that mature mammalian RBCs have no internal membrane-bound organelles, somewhat simplifies proteomics analysis of the plasma membrane and the fact that it has no nucleus disqualifies microarray based methods. Proteomics has the potential to provide a better understanding of this critical inter-face, and thereby assist in identifying new approaches to diseases. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 420
页数:18
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