Identification of the binding site on glycophorin A for Plasmodium falciparum EBA-175 / 南方医科大学学报
Journal of Southern Medical University
; (12): 1696-1698, 2007.
Article
in Zh
| WPRIM
| ID: wpr-281559
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To identify the binding site on glycophorin A (GPA) for EBA-175 to provide clue for developing short peptide vaccine and therapeutic agents against Plasmodium falciparum.</p><p><b>METHODS</b>With the recombinant protein of EBA-175 as the target molecule, the mimetic peptides of GPA were screened from a 12-mer random peptide library. Three rounds of biopanning were carried out, and enzyme-linked immunosorbent assay (ELISA), competitive ELISA, Dot-ELISA and Western blotting used to evaluate the binding between the phage-borne peptides and EBA-175. The insert DNA sequences of positive clones were determined and their amino acid sequences deduced.</p><p><b>RESULTS</b>Thirty clones from the third round were randomly selected, of which 27 were found positive by sandwich ELISA. Competitive ELISA proved that most of the phage-borne peptides could competitively inhibit the binding of antibody (EBA-175 Ab) with EBA-175. Analysis of DNA and amino acid sequences indicated that 24 positive phage clones contained the conservative sequence of IRR, which was highly homologous with the 114-116 amino acids of GPA.</p><p><b>CONCLUSION</b>These phage-displayed peptides can bind with EBA-175, and the amino acid sequence IRR might play an important role in the binding between EBA-175 and GPA.</p>
Full text:
1
Index:
WPRIM
Main subject:
Plasmodium falciparum
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Binding Sites
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Glycophorins
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Enzyme-Linked Immunosorbent Assay
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Protozoan Proteins
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Chemistry
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Sequence Analysis, DNA
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Peptide Library
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Sequence Analysis, Protein
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Metabolism
Limits:
Humans
Language:
Zh
Journal:
Journal of Southern Medical University
Year:
2007
Type:
Article