Originally published In Press as doi:10.1074/mcp.M300114-MCP200 on November 28, 2003.
Molecular & Cellular Proteomics 3:156-166, 2004.
© 2004 by The American Society for Biochemistry and Molecular Biology, Inc.
Research
Proteomic Analysis of the Systemic Immune Response of Drosophila*
Francine Levy ,
Philippe Bulet , and
Laurence Ehret-Sabatier ,¶
From the Institut de Biologie Moléculaire et Cellulaire, 15 rue René Descartes, 67084 Strasbourg Cedex, France
Improvements in two-dimensional gel electrophoresis, mass spectrometry, and bioinformatics provide new tools to characterize proteins involved in a physiological process, such as the immune response of the insect model Drosophila melanogaster. Profiling of the proteins present in the hemolymph (insect blood) of noninfected flies versus flies infected with bacteria or fungi was performed by two-dimensional gel electrophoresis, silver or Coomassie staining, and image analysis. Through this differential analysis, more than 70 out of 160 spots were up- or down-regulated by at least 5-fold after microbial infection. Coomassie staining, in-gel digestion, and database searches yielded the identity of a series of proteins that are directly involved in the Drosophila immune system. This included proteases, protease inhibitors, and recognition molecules such as prophenoloxydase-activating enzymes, serpins, and Gram-negative binding protein-like. Proteins with a potential function in the immune response were also identified, such as an odorant binding protein, peptidylglycine -hydroxylating monooxygenase, and transferrin, affording new candidates for further investigation of innate immune mechanisms. Moreover, several molecules resulting from the cleavage of proteins were detected after the fungal infection. Altogether, this first differential proteomic analysis of the immune response of Drosophila paves the way for the study of proteins affected during innate immunity.
¶ To whom correspondence should be addressed. Tel.: 33-(0)-388-41-70-62; Fax: 33-(0)-388-60-69-22; E-mail: L.Sabatier{at}ibmc.u-strasbg.fr

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
F Ponton, T Lefevre, C Lebarbenchon, F Thomas, H.D Loxdale, L Marche, L Renault, M.J Perrot-Minnot, and D.G Biron
Do distantly related parasites rely on the same proximate factors to alter the behaviour of their hosts?
Proc R Soc B,
November 22, 2006;
273(1603):
2869 - 2877.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Badariotti, M. Kypriotou, C. Lelong, M.-P. Dubos, E. Renard, P. Galera, and P. Favrel
The Phylogenetically Conserved Molluscan Chitinase-like Protein 1 (Cg-Clp1), Homologue of Human HC-gp39, Stimulates Proliferation and Regulates Synthesis of Extracellular Matrix Components of Mammalian Chondrocytes
J. Biol. Chem.,
October 6, 2006;
281(40):
29583 - 29596.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Karlsson, A. M. Korayem, C. Scherfer, O. Loseva, M. S. Dushay, and U. Theopold
Proteomic Analysis of the Drosophila Larval Hemolymph Clot
J. Biol. Chem.,
December 10, 2004;
279(50):
52033 - 52041.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
O. Loseva and Y. Engstrom
Analysis of Signal-dependent Changes in the Proteome of Drosophila Blood Cells During an Immune Response
Mol. Cell. Proteomics,
August 1, 2004;
3(8):
796 - 808.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2004 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|