Literature DB >> 11796121

Characterisation of global protein expression by two-dimensional electrophoresis and mass spectrometry: proteomics of Toxoplasma gondii.

A M Cohen1, K Rumpel, G H Coombs, J M Wastling.   

Abstract

The development of tools for the analysis of global gene expression is vital for the optimal exploitation of the data on parasite genomes that are now being generated in abundance. Recent advances in two-dimensional electrophoresis (2-DE), mass spectrometry and bioinformatics have greatly enhanced the possibilities for mapping and characterisation of protein populations. We have employed these developments in a proteomics approach for the analysis of proteins expressed in the tachyzoite stage of Toxoplasma gondii. Over 1000 polypeptides were reproducibly separated by high-resolution 2-DE using the pH ranges 4-7 and 6-11. Further separations using narrow range gels suggest that at least 3000-4000 polypeptides should be resolvable by 2-DE using multiple single pH unit gels. Mass spectrometry was used to characterise a variety of protein spots on the 2-DE gels. Peptide mass fingerprints, acquired by matrix-assisted laser desorption/ionisation-(MALDI) mass spectrometry, enabled unambiguous protein identifications to be made where full gene sequence information was available. However, interpretation of peptide mass fingerprint data using the T. gondii expressed sequence tag (EST) database was less reliable. Peptide fragmentation data, acquired by post-source decay mass spectrometry, proved a more successful strategy for the putative identification of proteins using the T. gondii EST database and protein databases from other organisms. In some instances, several protein spots appeared to be encoded by the same gene, indicating that post-translational modification and/or alternative splicing events may be a common feature of functional gene expression in T. gondii. The data demonstrate that proteomic analyses are now viable for T. gondii and other protozoa for which there are good EST databases, even in the absence of complete genome sequence. Moreover, proteomics is of great value in interpreting and annotating EST databases.

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Year:  2002        PMID: 11796121     DOI: 10.1016/s0020-7519(01)00308-3

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  27 in total

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2.  Proteomic analysis of Toxoplasma gondii KI-1 tachyzoites.

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3.  OmcF, a putative c-Type monoheme outer membrane cytochrome required for the expression of other outer membrane cytochromes in Geobacter sulfurreducens.

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4.  Genetic and proteomic analysis of the MHC class I repertoire from four ovine haplotypes.

Authors:  Keith T Ballingall; Despoina Miltiadou; Zhong-Wei Chai; Kevin McLean; Mara Rocchi; Raja Yaga; Declan J McKeever
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5.  The opportunistic pathogen Toxoplasma gondii deploys a diverse legion of invasion and survival proteins.

Authors:  Xing W Zhou; Björn F C Kafsack; Robert N Cole; Phil Beckett; Rong F Shen; Vern B Carruthers
Journal:  J Biol Chem       Date:  2005-07-07       Impact factor: 5.157

6.  RNG1 is a late marker of the apical polar ring in Toxoplasma gondii.

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7.  Identification of the cross-reactive and species-specific antigens between Neospora caninum and Toxoplasma gondii tachyzoites by a proteomics approach.

Authors:  Houshuang Zhang; Eung-Goo Lee; Longzheng Yu; Suguru Kawano; Penglong Huang; Min Liao; Osamu Kawase; Guohong Zhang; Jinlin Zhou; Kozo Fujisaki; Yoshifumi Nishikawa; Xuenan Xuan
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8.  Proteomics in Vaccinology and Immunobiology: An Informatics Perspective of the Immunone.

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Journal:  J Biomed Biotechnol       Date:  2003

9.  Identification and characterization of a Neospora caninum microneme-associated protein (NcMIC4) that exhibits unique lactose-binding properties.

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Journal:  Infect Immun       Date:  2004-08       Impact factor: 3.441

Review 10.  Toxoplasma gondii proteomics.

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Journal:  Expert Rev Proteomics       Date:  2009-06       Impact factor: 3.940

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