Literature DB >> 18314734

Analyzing import intermediates of mitochondrial proteins by blue native gel electrophoresis.

Thomas Waizenegger1, Doron Rapaport.   

Abstract

Blue native gel electrophoresis (BNGE) is a powerful tool for analyzing native protein complexes from biological membranes as well as water-soluble proteins. It can be used for determining relative molecular masses of protein complexes and their subunit composition and for the detection of subcomplexes. We describe the analysis by BNGE of in vitro import reactions composed of radiolabeled precursor proteins and isolated mitochondria. Such an analysis is a powerful tool to follow import intermediates and to study assembly of protein complexes. Analysis of import reactions by BNGE provides information on the molecular mass of the complex with which the imported precursor is associated. In addition, components of such a complex can be identified by incubating the mitochondrial lysate with either soluble antibodies or antibodies coupled to protein A matrix. The binding of soluble antibodies to specific complexes results in an observed shift in their apparent molecular mass (antibody shift). Alternatively, addition of matrix-bound antibodies followed by removal of the matrix from the mixture will result in depletion of the specific complex from the mitochondrial lysate (antibody depletion). The experimental details of these techniques are described.

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Year:  2007        PMID: 18314734     DOI: 10.1007/978-1-59745-365-3_21

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Formation of the redox cofactor centers during Cox1 maturation in yeast cytochrome oxidase.

Authors:  Oleh Khalimonchuk; Megan Bestwick; Brigitte Meunier; Talina C Watts; Dennis R Winge
Journal:  Mol Cell Biol       Date:  2009-12-07       Impact factor: 4.272

  1 in total

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