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Substitution-Inert Polynuclear Platinum Complexes Inhibit Reverse Transcription Preferentially in RNA Triplex-Forming Templates
J. Malina, NP. Farrell, V. Brabec
Language English Country United States
Document type Journal Article
- MeSH
- Coordination Complexes chemistry MeSH
- Nucleic Acid Conformation MeSH
- Platinum chemistry MeSH
- Antineoplastic Agents chemistry MeSH
- Reverse Transcription drug effects MeSH
- RNA chemistry MeSH
- Base Sequence MeSH
- Publication type
- Journal Article MeSH
RNA triplexes are significant tertiary structure motifs that are found in many functional RNAs. Hence, small molecules capable of recognition, binding, and stabilization of the triple-helical RNA structures are emerging as attractive potential molecular biology tools and therapeutic agents. Here, we utilize methods of molecular biology and biophysics to study the interactions of a series of antitumor substitution-inert polynuclear platinum complexes (SI-PPCs) with triple-helical RNA structures. We show that SI-PPCs recognize and stabilize RNA triplexes and inhibit reverse transcription preferentially in the RNA template prone to the triplex formation. These so far unexplored properties of SI-PPCs suggest that the targeting of triple-stranded regions in RNA might contribute to the biological effects of SI-PPCs.
Czech Academy of Sciences Institute of Biophysics Kralovopolska 135 Brno CZ 61265 Czech Republic
Department of Chemistry Virginia Commonwealth University Richmond Virginia 23284 2006 United States
References provided by Crossref.org
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