Membrane protein synthesis in cell-free systems: From bio-mimetic systems to bio-membranes

被引:112
|
作者
Sachse, Rita [1 ]
Dondapati, Srujan K. [1 ]
Fenz, Susanne F. [2 ]
Schmidt, Thomas [3 ]
Kubick, Stefan [1 ]
机构
[1] Fraunhofer Inst Cell Therapy & Immunol IZI, Branch Bioanalyt & Bioproc Potsdam Golm, D-14476 Potsdam, Germany
[2] Univ Wurzburg, Bioctr, Dept Cell & Dev Biol, D-14476 Wurzburg, Germany
[3] Leiden Univ, Leiden Inst Phys, NL-2300 RA Leiden, Netherlands
关键词
Membrane proteins; Cell-free systems; Biological membranes; Biomimetics; Microsomes; FREE TRANSLATION SYSTEM; NANOSCALE PHOSPHOLIPID-BILAYERS; MITOCHONDRIAL ADP/ATP CARRIER; FREE EXPRESSION; ESCHERICHIA-COLI; IN-VITRO; NANOLIPOPROTEIN PARTICLES; DOG PANCREAS; ROUGH MICROSOMES; AQUAPORIN Z;
D O I
10.1016/j.febslet.2014.06.007
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
When taking up the gauntlet of studying membrane protein functionality, scientists are provided with a plethora of advantages, which can be exploited for the synthesis of these difficult-to-express proteins by utilizing cell-free protein synthesis systems. Due to their hydrophobicity, membrane proteins have exceptional demands regarding their environment to ensure correct functionality. Thus, the challenge is to find the appropriate hydrophobic support that facilitates proper membrane protein folding. So far, various modes of membrane protein synthesis have been presented. Here, we summarize current state-of-the-art methodologies of membrane protein synthesis in biomimetic-supported systems. The correct folding and functionality of membrane proteins depend in many cases on their integration into a lipid bilayer and subsequent posttranslational modification. We highlight cell-free systems utilizing the advantages of biological membranes. (C) 2014 The Authors. Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:2774 / 2781
页数:8
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