Light-Triggered Green Fluorescent Protein Silencing in Human Keratinocytes in Culture Using Antisense Oligonucleotides Coupled to a Photoreactive Ruthenium(II) Complex
A photoreactive ruthenium(II) complex that contains two tetraazaphenanthrene (TAP) and one phenanthroline (phen) ligands was synthesized and then tethered to (antisense) oligonucleotides (Ru–ASO) to target a destabilized GFP (dGFP). The specificity of the photoreaction of this Ru–ASO conjugate was s...
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Veröffentlicht in: | ChemPlusChem (Weinheim, Germany) Germany), 2014-11, Vol.79 (11), p.1597-1604 |
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Sprache: | eng |
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Zusammenfassung: | A photoreactive ruthenium(II) complex that contains two tetraazaphenanthrene (TAP) and one phenanthroline (phen) ligands was synthesized and then tethered to (antisense) oligonucleotides (Ru–ASO) to target a destabilized GFP (dGFP). The specificity of the photoreaction of this Ru–ASO conjugate was studied in vitro by polyacrylamide gel electrophoresis (PAGE) experiments in denaturing conditions. Other nonspecific Ru–ASO conjugates were also prepared and evaluated with human keratinocytes that expressed dGFP. An illumination‐dependent cytotoxicity was observed for most Ru–ASO conjugates that varied from 10 to almost 40 %, but only the specific Ru–ASO conjugate was able to significantly reduce GFP expression in illuminated cells.
Silence, please: The specific ruthenium(1,4,5,8‐tetraazaphenanthrene)–antisense oligodeoxyribonucleotide (Ru(TAP)–ASO) conjugate is able to significantly reduce green fluorescent protein (GFP) expression after Ru–ASO visible excitation in treated cells (see figure). |
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ISSN: | 2192-6506 2192-6506 |
DOI: | 10.1002/cplu.201402212 |