Preparation of ribosomes loaded with truncated nascent proteins to study ribosome binding to mammalian mitochondria

被引:4
作者
MacKenzie, James A.
Payne, R. Mark
机构
[1] Indiana Univ, Sch Med, Dept Pediat, Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[2] SUNY Coll Oswego, Dept Biol Sci, Oswego, NY 13126 USA
关键词
ribosomes; ribosome-nascent chain complex; in vitro translation; mitochondria; protein targeting;
D O I
10.1016/j.mito.2006.01.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Supporting a co-translational model of protein import into mitochondria, we have previously shown that ribosome-nascent chain complexes (RNCs) specifically bind to mitochondria. When producing RNCs using the rabbit reticulocyte lysate in vitro translation system, it was necessary to maximize ribosome loading with truncated nascent proteins because it had a direct impact on RNC binding. We describe here the optimal conditions for preparing RNCs. We show that translation temperature and reaction time are two critical factors, with 30 T and 15 min being optimal, respectively. We also show that transcription reactions can be used directly in the translation reaction to create RNCs. (c) 2006 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
引用
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页码:64 / 70
页数:7
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