Literature DB >> 16213502

Single chain antibody against the common epitope of mutant p53 restores wild-type activity to mutant p53 protein.

Sara Orgad1, Naomi Goldfinger, Gerald Cohen, Varda Rotter, Beka Solomon.   

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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Year:  2005        PMID: 16213502     DOI: 10.1016/j.febslet.2005.09.031

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  1 in total

1.  Cell surface enzyme attachment is mediated by family 37 carbohydrate-binding modules, unique to Ruminococcus albus.

Authors:  Anat Ezer; Erez Matalon; Sadanari Jindou; Ilya Borovok; Nof Atamna; Zhongtang Yu; Mark Morrison; Edward A Bayer; Raphael Lamed
Journal:  J Bacteriol       Date:  2008-10-17       Impact factor: 3.490

  1 in total

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