FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Harder, B., Schomburg, A., Pflanz, R., Küstner, K., Gerlach, N., Schuh, R. (2008). TEV protease-mediated cleavage in Drosophila as a tool to analyze protein functions in living organisms.  BioTechniques 44(6): 765--772.
FlyBase ID
FBrf0204684
Publication Type
Research paper
Abstract
Drosophila provides a powerful experimental system to analyze gene functions in a multi-cellular organism. Here we describe an in vivo method that interferes with the integrity of selected proteins through site-specific cleavage in Drosophila. The technique is based on the highly specific seven-amino-acid recognition site of the tobacco etch virus (TEV) protease. We established transgenic fly lines that direct TEV protease expression in various tissues without affecting fly viability. The insertion of the TEV protease recognition site in defined positions of target proteins mediates their sequence-specific cleavage after controlled TEV protease expression in the fly. Thereby, this technique is a powerful tool that allows the in vivo manipulation of selected proteins in a time- and tissue-specific manner.
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    BioTechniques
    Title
    BioTechniques
    Publication Year
    1983-
    ISBN/ISSN
    0736-6205
    Data From Reference