Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen

The major aim of this study was to characterize a soluble Plasmodium falciparum antigen from the plasma of malaria-infected humans and Plasmodium falciparum culture supernatants, using immunoabsorbent techniques and Western blotting. An Mr 60-kDa protein was isolated from the plasma of patients with...

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Main Authors: A. Rodríguez-Acosta, N.G. Domínguez, I. Aguilar, M.E. Girón
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 1998-09-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900008
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spelling doaj-f287c616c6a1427e817bc2b084c4ad142020-11-24T22:26:00ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X1998-09-01319114910.1590/S0100-879X1998000900008Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigenA. Rodríguez-AcostaN.G. DomínguezI. AguilarM.E. GirónThe major aim of this study was to characterize a soluble Plasmodium falciparum antigen from the plasma of malaria-infected humans and Plasmodium falciparum culture supernatants, using immunoabsorbent techniques and Western blotting. An Mr 60-kDa protein was isolated from the plasma of patients with Plasmodium falciparum malaria by affinity chromatography using rabbit anti-Proteus spp GDH(NADP+) serum as ligand. This protein, present in plasma of patients with acute Plasmodium falciparum infection, in Plasmodium falciparum culture supernatants, and in immune complexes, was tested with Plasmodium falciparum malaria hyperimmune serum from patients living in hyperendemic areas and rabbit anti-Proteus spp GDH(NADP+) serum prepared in the laboratory. In this report, we describe the results of a study showing that parasite GDH(NADP+) can be used to detect the presence of Plasmodium falciparum. It appears that this technique permits the chromatographic detection of a Plasmodium falciparum excretion antigen that may be used in the production of monoclonal antibodies to improve immunodiagnostic assays for the detection of antigenemia, and opens the possibility of its use as a non-microscopic screening method.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900008glutamate-dehydrogenasePlasmodium falciparumexoantigenssoluble antigensmalariaantigenic enzymes
collection DOAJ
language English
format Article
sources DOAJ
author A. Rodríguez-Acosta
N.G. Domínguez
I. Aguilar
M.E. Girón
spellingShingle A. Rodríguez-Acosta
N.G. Domínguez
I. Aguilar
M.E. Girón
Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
Brazilian Journal of Medical and Biological Research
glutamate-dehydrogenase
Plasmodium falciparum
exoantigens
soluble antigens
malaria
antigenic enzymes
author_facet A. Rodríguez-Acosta
N.G. Domínguez
I. Aguilar
M.E. Girón
author_sort A. Rodríguez-Acosta
title Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
title_short Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
title_full Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
title_fullStr Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
title_full_unstemmed Characterization of Plasmodium falciparum glutamate dehydrogenase-soluble antigen
title_sort characterization of plasmodium falciparum glutamate dehydrogenase-soluble antigen
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 0100-879X
1414-431X
publishDate 1998-09-01
description The major aim of this study was to characterize a soluble Plasmodium falciparum antigen from the plasma of malaria-infected humans and Plasmodium falciparum culture supernatants, using immunoabsorbent techniques and Western blotting. An Mr 60-kDa protein was isolated from the plasma of patients with Plasmodium falciparum malaria by affinity chromatography using rabbit anti-Proteus spp GDH(NADP+) serum as ligand. This protein, present in plasma of patients with acute Plasmodium falciparum infection, in Plasmodium falciparum culture supernatants, and in immune complexes, was tested with Plasmodium falciparum malaria hyperimmune serum from patients living in hyperendemic areas and rabbit anti-Proteus spp GDH(NADP+) serum prepared in the laboratory. In this report, we describe the results of a study showing that parasite GDH(NADP+) can be used to detect the presence of Plasmodium falciparum. It appears that this technique permits the chromatographic detection of a Plasmodium falciparum excretion antigen that may be used in the production of monoclonal antibodies to improve immunodiagnostic assays for the detection of antigenemia, and opens the possibility of its use as a non-microscopic screening method.
topic glutamate-dehydrogenase
Plasmodium falciparum
exoantigens
soluble antigens
malaria
antigenic enzymes
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000900008
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