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Resources » Paper

Nilsen TW et al. (1988) Proc Natl Acad Sci U S A "Cloning and characterization of a potentially protective antigen in lymphatic filariasis."

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  • Comments on Nilsen TW et al. (1988) Proc Natl Acad Sci U S A "Cloning and characterization of a potentially protective antigen in lymphatic filariasis." (0)

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    PMID:
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    Publication type:
    Journal_article
    WormBase ID:
    WBPaper00048606

    Nilsen TW, Maroney PA, Goodwin RG, Perrine KG, Denker JA, Nanduri J, & Kazura JW (1988). Cloning and characterization of a potentially protective antigen in lymphatic filariasis. Proc Natl Acad Sci U S A, 85, 3604-7. doi:10.1073/pnas.85.10.3604

    To facilitate biochemical studies of protective filarial antigens, a lambda gt11 cDNA library was constructed from Brugia malayi adult mRNA and screened with rabbit sera that recognizes a limited set of filarial antigens of approximately 25, 42, 60, and 112 kDa. Antigens of approximately equal to 25 and approximately equal to 60 kDa have been shown previously to induce enhanced clearance of microfilaremia in mice. A 154-base pair clone detected by immunological reactivity was used to isolate by hybridization a nearly full-length cDNA clone of 1.8 kilobases. Nucleotide-sequence analysis indicated that this clone was derived from a mRNA encoding a 63-kDa antigen. A fusion polypeptide containing 37 kDa of the Escherichia coli TrpE protein (anthranilate synthase) and 55 kDa of the cloned protein was recognized in immunoblot experiments with antisera raised against a partially purified preparation of the approximately equal to 60-kDa protective filarial antigen. These data relate the cloned antigen to a potentially protective antigen in lymphatic filariasis.


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