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    In-cell assembly of scFv from human thyroid-infiltrating B cells.

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    Authors
    Chapal, N
    Bouanani, M
    Embleton, Jim
    Navarro-Teulon, I
    Biard-Piechaczyk, M
    Pau, B
    Peraldi-Roux, S
    Affiliation
    CNRS UMR 9921, Faculté de Pharmacie, Montpellier, France.
    Issue Date
    1997-09
    
    Metadata
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    Abstract
    The construction of a large library of single-chain Fv (scFv) antibody fragments involves a random assortment of heavy and light chains. Although useful for the production of recombinant antibodies, this method is not adapted to the study of the autoantibody repertoire formed in vivo during autoimmune diseases. To attain this objective, we describe the use of the in-cell PCR together with Cre-recombination applied, to our knowledge, for the first time to human B cells to obtain in situ pairing of the variable (V) region genes of the immunoglobulin heavy (H) and light (L) chains. Our method is based on amplification and recombination of the VH and VL genes within CD19+ B cells isolated from human thyroid tissue. Nested primers were designed to amplify the known major human VH and VL gene families. After reverse transcription PCR and three rounds of PCR including recombination between VH and VL using the Cre-loxP system, we obtained a unique 800-bp band corresponding in size to scFv fragments. We provide evidence that recombination between VH and VL genes occurred inside the same cell. This in-cell amplification and association procedure is a potentially useful tool for the study of autoantibody gene families and the VH/VL pairing that occurs during the autoimmune process.
    Citation
    In-cell assembly of scFv from human thyroid-infiltrating B cells. 1997, 23 (3):518-24 BioTechniques
    Journal
    BioTechniques
    URI
    http://hdl.handle.net/10541/94912
    PubMed ID
    9298226
    Type
    Article
    Language
    en
    ISSN
    0736-6205
    Collections
    All Paterson Institute for Cancer Research

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