Mapping of Two Dominant Sites of VP35 of Marburg Virus

Five types of anti-VP35 monoclonal antibodies (MAbs), four immune sera against Marburg virus (MBGV), and 11 overlapping recombinant VP35 fragments were used to map the epitopes for VP35 of MBGV. The purified full-size recombinant VP35 was highly immunogenic and retained the B-cell epitopes that were...

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Veröffentlicht in:Viral immunology 2002-01, Vol.15 (3), p.481-492
Hauptverfasser: Sorokin, A.V., Kazachinskaia, E.I., Ivanova, A.V., Kachko, A.V., Netesov, S.V., Bukreyev, A.A., Loktev, V.B., Razumov, I.A.
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Sprache:eng
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Zusammenfassung:Five types of anti-VP35 monoclonal antibodies (MAbs), four immune sera against Marburg virus (MBGV), and 11 overlapping recombinant VP35 fragments were used to map the epitopes for VP35 of MBGV. The purified full-size recombinant VP35 was highly immunogenic and retained the B-cell epitopes that were identical to those of the viral VP35. Two major sites on VP35 and a set of truncated VP35 fragments were found by use of an enzyme immunoassay and immunoblot. Site I was located in a region between amino acids 1 and 174 of the VP35 sequence, and only polyclonal antibodies (PAbs) against MBGV recognized epitopes at this site. Site II was mapped by use of anti-VP35 MAbs to the region between amino acid residues 167 and 278 of VP35. Amino acids 252-278 of VP35 might be involved in the formation of the epitopes for MAbs. B-cell epitopes were not found on the C-terminus of VP35 by use of PAbs or MAbs.
ISSN:0882-8245
1557-8976
DOI:10.1089/088282402760312359