Ribonuclease-neutralized pancreatic microsomal membranes from livestock for in vitro co-translational protein translocation

被引:7
|
作者
Vermeire, Kurt [1 ]
Allan, Susanne [2 ]
Provinciael, Becky [1 ]
Hartmann, Enno [2 ]
Kalies, Kai-Uwe [2 ]
机构
[1] KU Leuven Univ Leuven, Dept Microbiol & Immunol, Lab Virol & Chemotherapy, Rega Inst Med Res, B-63000 Leuven, Belgium
[2] Univ Lubeck, Inst Biol, Ctr Struct & Cell Biol Med CSCM, D-23538 Lubeck, Germany
关键词
Cell-free protein translation; Pancreatic microsomes; Mammalian ER membranes; Ribonuclease; Cyclotriazadisulfonamide (CADA); Translocation inhibitor; ENDOPLASMIC-RETICULUM; CHOLERA-TOXIN; RAT-LIVER; SEC61P; YEAST;
D O I
10.1016/j.ab.2015.05.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here, we demonstrate that pancreatic microsomal membranes from pigs, sheep, or cattle destined for human consumption can be used as a valuable and ethically correct alternative to dog microsomes for cell-free protein translocation. By adding adequate ribonuclease (RNase) inhibitors to the membrane fraction, successful in vitro co-translational translocation of wild-type and chimeric pre-prolactin into the lumen of rough microsomes was obtained. In addition, the human type I integral membrane proteins CD4 and VCAM-1 were efficiently glycosylated in RNase-treated microsomes. Thus, RNase-neutralized pancreatic membrane fractions from pig, cow, or sheep are a cheap, easily accessible, and fulfilling alternative to canine microsomes. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:102 / 104
页数:3
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