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Novel two‐stage screening procedure leads to the identification of a new class of transfection enhancers
Author(s) -
Neukamm Birgit,
Weimann Andreas,
Wu Shuling,
Danevad Margrete,
Lang Christine,
Geßner Reinhard
Publication year - 2006
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.887
Subject(s) - transfection , reporter gene , enhancer , cell culture , chemistry , doxepin , microbiology and biotechnology , biology , gene , pharmacology , biochemistry , gene expression , genetics
Background Non‐viral gene transfer efficiency is low as compared to viral vector systems. Here we describe the discovery of new drugs that are capable of enhancing non‐viral gene transfer into mammalian cells using a novel two‐stage screening procedure. Methods First, potential candidates are preselected from a molecular library at various concentrations by a semi‐automated yeast transfection screen (YTS). The maximal transfection efficiency of every positive drug is subsequently determined in independent experiments at the optimal concentration and compared to the inhibitory effect of the drug on cell growth (IC50). In a subsequent mammalian cell transfection screen (MTS), the maximal transfection efficiency and the IC50 are determined for all preselected drugs using a human cell line and a luciferase reporter gene construct. Results Employing our novel system we have been able to identify a new class of transfection enhancers, the tricyclic antidepressants (i.e. doxepin, maprotiline, desipramine and amoxapine). All positive drugs enhanced gene transfer in both yeast and human cell lines, but lower concentrations were sufficient for mammalian cells. With a triple combination of doxepin, amoxapine and chloroquine we obtained a transfection efficiency that exceeded that of chloroquine, one of the best‐known transfection enhancers of mammalian cells, by nearly one order of magnitude. Conclusions Non‐viral gene transfer efficiency can be increased significantly using new transfection enhancers that are identified by a novel, semi‐automated two‐stage screening system employing yeast cells in the first and specific human target cells in the second round. Copyright © 2006 John Wiley & Sons, Ltd.