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Identification of antigenic Brugia adult worm proteins by peptide mass fingerprinting.

Identifieur interne : 003474 ( Ncbi/Checkpoint ); précédent : 003473; suivant : 003475

Identification of antigenic Brugia adult worm proteins by peptide mass fingerprinting.

Auteurs : Tiffany Weinkopff [États-Unis] ; James A. Atwood ; George A. Punkosdy ; Delynn Moss ; D Brent Weatherly ; Ron Orlando ; Patrick Lammie

Source :

RBID : pubmed:19537848

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English descriptors

Abstract

With the recent completion of the Brugia malayi genome, proteomics offers a new resource for a deeper understanding of the biology of filarial parasites. We employed 2-dimensional (2D) gel electrophoresis followed by peptide mass fingerprinting on a matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometer to identify Brugia adult worm proteins and then determined which proteins were recognized by the host humoral immune response. We identified 18 unique proteins, several of which were determined to be antigenic by immunoblot. The proteins identified here may contribute to future studies to analyze the transmission and pathogenesis of lymphatic filariasis.

DOI: 10.1645/GE-2083.1
PubMed: 19537848


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pubmed:19537848

Le document en format XML

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<nlm:affiliation>Department of Cell Biology, 724 Biological Sciences Building, University of Georgia, Athens, Georgia 30602, USA.</nlm:affiliation>
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<term>Antibodies, Helminth (blood)</term>
<term>Antigens, Helminth (analysis)</term>
<term>Antigens, Helminth (chemistry)</term>
<term>Antigens, Helminth (immunology)</term>
<term>Brugia pahangi (chemistry)</term>
<term>Brugia pahangi (immunology)</term>
<term>Electrophoresis, Gel, Two-Dimensional</term>
<term>Electrophoresis, Polyacrylamide Gel</term>
<term>Elephantiasis, Filarial (blood)</term>
<term>Elephantiasis, Filarial (immunology)</term>
<term>Elephantiasis, Filarial (parasitology)</term>
<term>Gerbillinae</term>
<term>Helminth Proteins (analysis)</term>
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<term>Helminth Proteins (immunology)</term>
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<term>Image Processing, Computer-Assisted</term>
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<term>Molecular Sequence Data</term>
<term>Proteomics</term>
<term>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</term>
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<term>Antigènes d'helminthe (analyse)</term>
<term>Antigènes d'helminthe (immunologie)</term>
<term>Brugia pahangi ()</term>
<term>Brugia pahangi (immunologie)</term>
<term>Données de séquences moléculaires</term>
<term>Filariose lymphatique (immunologie)</term>
<term>Filariose lymphatique (parasitologie)</term>
<term>Filariose lymphatique (sang)</term>
<term>Gerbillinae</term>
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<term>Protéines d'helminthes ()</term>
<term>Protéines d'helminthes (analyse)</term>
<term>Protéines d'helminthes (immunologie)</term>
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<term>Séquence d'acides aminés</term>
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<term>Brugia pahangi</term>
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<term>Immunotransfert</term>
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<div type="abstract" xml:lang="en">With the recent completion of the Brugia malayi genome, proteomics offers a new resource for a deeper understanding of the biology of filarial parasites. We employed 2-dimensional (2D) gel electrophoresis followed by peptide mass fingerprinting on a matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF) mass spectrometer to identify Brugia adult worm proteins and then determined which proteins were recognized by the host humoral immune response. We identified 18 unique proteins, several of which were determined to be antigenic by immunoblot. The proteins identified here may contribute to future studies to analyze the transmission and pathogenesis of lymphatic filariasis.</div>
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