Characterization of the Drosophila melanogaster Mitochondrial Proteome

Jana Alonso, Javier M. Rodriguez, Luis Alberto Baena-López, and Juan F. Santarén*
Centro de Biologa Molecular Severo Ochoa, CSIC-UAM, Universidad Autnoma de Madrid, Cantoblanco, 28049-Madrid, Spain
J. Proteome Res., 2005, 4 (5), pp 1636–1645
DOI: 10.1021/pr050130c
Publication Date (Web): September 16, 2005
Copyright © 2005 American Chemical Society
*

 To whom correspondence should be addressed. Tel:  34-1-914978447. Fax:  34-1-914974799. E-mail:  jfsantaren@cbm.uam.es.

Abstract

Abstract Image

We have combined high-resolution two-dimensional (2-D) gel electrophoresis with mass spectrometry with the aim of identifying proteins represented in the 2-D gel database of Drosophila melanogaster mitochondria. First, we purified mitochondria from third instar Drosophila larvae and constructed a high-resolution 2-D gel database containing 231 silver-stained polypeptides. Next, we carried out preparative 2-D PAGE to isolate some of the polypeptides and characterize them by MALDI-TOF analysis. Using this strategy, we identified 66 mitochondrial spots in the database, and in each case confirmed their identity by MALDI-TOF/TOF analysis. In addition, we generated antibodies against two of the mitochondrial proteins as tools for characterizing the organelle.

Keywords: Drosophila • mitochondria • proteomics • 2D gels • MALDI-TOF

Tools

SciFinder Links

SciFinder subscribers:  Click to sign in | Not a SciFinder subscriber? Learn more at www.cas.org

History

  • Published In Issue October 10, 2005
  • Received May 6, 2005

Recommend & Share

Related Content

Other ACS content by these authors: