Detection of a Plasmodium vivax erythrocyte binding protein by flow cytometry

Tuan  Tran, Alberto Moreno, Syed S. Yazdani, Chetan E. Chitnis, John W. Barnwell, Mary R. Galinski

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Background: The malaria parasite Plasmodium vivax preferentially invades reticulocytes. It is therefore relevant for vaccine development purposes to identify and characterize P. vivax proteins that bind specifically to the surface of reticulocytes. We have developed a two-color flow cytometric erythrocyte binding assay (F-EBA) that has several advantages over traditional erythrocyte binding assays (T-EBAs) used in malaria research. We demonstrate the use of F-EBA using the P. vivax Duffy binding protein region II (PvDBP-RII) recombinant protein as a model. This protein binds to all erythrocytes that express the Duffy receptor (Fy) and discriminates binding between normocytes and reticulocytes. Methods: F-EBAs were performed by incubating freshly isolated Aotus nancymai, Macaca mulatta, Saimiri boliviensis, and human erythrocytes with PvDBP-RII, a fluorescent anti-His tag detection antibody, and thiazole orange before flow cytometric analysis. T-EBAs employing immunoblot detection with an anti-His antibody were performed concomitantly. Results: PvDBP-RII bound to A. nancymai, M. mulatta, and human Fy+ erythrocytes, but not human Fy- erythrocytes, by F-EBAs and T-EBAs. However, F-EBAs exhibited higher sensitivity and better concordance between experiments compared with T-EBAs. Conclusions: F-EBA is a rapid, simple, and reliable method for quantifying the ability of malaria proteins to bind to the surface of erythrocytes, F-EBA can discriminate binding between erythrocyte subpopulations without enrichment protocols and may be more reliable and sensitive than T-EBAs in identifying novel erythrocyte binding proteins.

Original languageEnglish (US)
Pages (from-to)59-66
Number of pages8
JournalCytometry Part A
Volume63
Issue number1
DOIs
StatePublished - Jan 2005
Externally publishedYes

Fingerprint

Plasmodium vivax
Flow Cytometry
Erythrocytes
Reticulocytes
Plasmodium Duffy antigen binding protein
Macaca mulatta
Malaria
Vivax Malaria
Saimiri
Proteins

Keywords

  • Duffy binding protein
  • Erythrocyte binding assay
  • Flow cytometry
  • Malaria
  • Plasmodium vivax
  • Reticulocyte

ASJC Scopus subject areas

  • Hematology
  • Cell Biology
  • Pathology and Forensic Medicine
  • Biophysics
  • Endocrinology

Cite this

Tran, T., Moreno, A., Yazdani, S. S., Chitnis, C. E., Barnwell, J. W., & Galinski, M. R. (2005). Detection of a Plasmodium vivax erythrocyte binding protein by flow cytometry. Cytometry Part A, 63(1), 59-66. https://doi.org/10.1002/cyto.a.20098

Detection of a Plasmodium vivax erythrocyte binding protein by flow cytometry. / Tran, Tuan ; Moreno, Alberto; Yazdani, Syed S.; Chitnis, Chetan E.; Barnwell, John W.; Galinski, Mary R.

In: Cytometry Part A, Vol. 63, No. 1, 01.2005, p. 59-66.

Research output: Contribution to journalArticle

Tran, T, Moreno, A, Yazdani, SS, Chitnis, CE, Barnwell, JW & Galinski, MR 2005, 'Detection of a Plasmodium vivax erythrocyte binding protein by flow cytometry', Cytometry Part A, vol. 63, no. 1, pp. 59-66. https://doi.org/10.1002/cyto.a.20098
Tran, Tuan  ; Moreno, Alberto ; Yazdani, Syed S. ; Chitnis, Chetan E. ; Barnwell, John W. ; Galinski, Mary R. / Detection of a Plasmodium vivax erythrocyte binding protein by flow cytometry. In: Cytometry Part A. 2005 ; Vol. 63, No. 1. pp. 59-66.
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abstract = "Background: The malaria parasite Plasmodium vivax preferentially invades reticulocytes. It is therefore relevant for vaccine development purposes to identify and characterize P. vivax proteins that bind specifically to the surface of reticulocytes. We have developed a two-color flow cytometric erythrocyte binding assay (F-EBA) that has several advantages over traditional erythrocyte binding assays (T-EBAs) used in malaria research. We demonstrate the use of F-EBA using the P. vivax Duffy binding protein region II (PvDBP-RII) recombinant protein as a model. This protein binds to all erythrocytes that express the Duffy receptor (Fy) and discriminates binding between normocytes and reticulocytes. Methods: F-EBAs were performed by incubating freshly isolated Aotus nancymai, Macaca mulatta, Saimiri boliviensis, and human erythrocytes with PvDBP-RII, a fluorescent anti-His tag detection antibody, and thiazole orange before flow cytometric analysis. T-EBAs employing immunoblot detection with an anti-His antibody were performed concomitantly. Results: PvDBP-RII bound to A. nancymai, M. mulatta, and human Fy+ erythrocytes, but not human Fy- erythrocytes, by F-EBAs and T-EBAs. However, F-EBAs exhibited higher sensitivity and better concordance between experiments compared with T-EBAs. Conclusions: F-EBA is a rapid, simple, and reliable method for quantifying the ability of malaria proteins to bind to the surface of erythrocytes, F-EBA can discriminate binding between erythrocyte subpopulations without enrichment protocols and may be more reliable and sensitive than T-EBAs in identifying novel erythrocyte binding proteins.",
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AB - Background: The malaria parasite Plasmodium vivax preferentially invades reticulocytes. It is therefore relevant for vaccine development purposes to identify and characterize P. vivax proteins that bind specifically to the surface of reticulocytes. We have developed a two-color flow cytometric erythrocyte binding assay (F-EBA) that has several advantages over traditional erythrocyte binding assays (T-EBAs) used in malaria research. We demonstrate the use of F-EBA using the P. vivax Duffy binding protein region II (PvDBP-RII) recombinant protein as a model. This protein binds to all erythrocytes that express the Duffy receptor (Fy) and discriminates binding between normocytes and reticulocytes. Methods: F-EBAs were performed by incubating freshly isolated Aotus nancymai, Macaca mulatta, Saimiri boliviensis, and human erythrocytes with PvDBP-RII, a fluorescent anti-His tag detection antibody, and thiazole orange before flow cytometric analysis. T-EBAs employing immunoblot detection with an anti-His antibody were performed concomitantly. Results: PvDBP-RII bound to A. nancymai, M. mulatta, and human Fy+ erythrocytes, but not human Fy- erythrocytes, by F-EBAs and T-EBAs. However, F-EBAs exhibited higher sensitivity and better concordance between experiments compared with T-EBAs. Conclusions: F-EBA is a rapid, simple, and reliable method for quantifying the ability of malaria proteins to bind to the surface of erythrocytes, F-EBA can discriminate binding between erythrocyte subpopulations without enrichment protocols and may be more reliable and sensitive than T-EBAs in identifying novel erythrocyte binding proteins.

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KW - Erythrocyte binding assay

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KW - Malaria

KW - Plasmodium vivax

KW - Reticulocyte

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