Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2052536 | FEBS Letters | 2005 | 7 Pages |
Abstract
Here, we describe the biological activity of ME1, a mouse single chain Fv fragment (scFv) against the common epitope of mutant p53, which is efficiently expressed in mammalian cells. We found that in vivo interaction of the conformational p53 mutant R175H protein with the scFv resulted in the acquisition of wild-type p53 characteristics, manifested in trans-activation of p21, as well as induction of apoptosis. Moreover, antibody binding leads to abrogation of the mutant p53 mediated “gain of function” as estimated by downregulation of EGR-1, a transcriptional target of mutant p53. These findings suggest that the scFv restores wild-type properties to mutant p53.
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Authors
Sara Orgad, Naomi Goldfinger, Gerald Cohen, Varda Rotter, Beka Solomon,