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               <dc:title>Parallel Clamps and Polypurine Hairpins (PPRH) for Gene Silencing and Triplex-Affinity Capture: Design, Synthesis, and Use</dc:title>
               <dc:creator>Aviñó Andrés, Anna</dc:creator>
               <dc:creator>Eritja i Casadellà, Ramon</dc:creator>
               <dc:creator>Ciudad i Gómez, Carlos Julián</dc:creator>
               <dc:creator>Noé Mata, Verónica</dc:creator>
               <dc:subject>ADN</dc:subject>
               <dc:subject>Teràpia genètica</dc:subject>
               <dc:subject>Reparació de l'ADN</dc:subject>
               <dc:subject>DNA</dc:subject>
               <dc:subject>Gene therapy</dc:subject>
               <dc:subject>DNA repair</dc:subject>
               <dc:description>Nucleic acid triplexes are formed when a DNA or RNA oligonucleotide binds to a polypurine-polypyrimidine-rich sequence. Triplexes have wide therapeutic applications such as gene silencing or site-specific mutagenesis. In addition, protocols based on triplex-affinity capture have been used for detecting nucleic acids in biosensing platforms. In this article, the design, synthesis, and use of parallel clamps and polypurine-reversed hairpins (PPRH) to bind to target polypyrimidine targets are described. The combination of the polypurine Watson-Crick strand with the triplex-forming strand in a single molecule produces highly stable triplexes allowing targeting of single- and double-stranded nucleic acid sequences. On the other hand, PPRHs are easily prepared and work at nanomolar range, like siRNAs, and at a lower concentration than that needed for antisense ODNs or TFOs. However, the stability of PPRHs is higher than that of siRNAs. In addition, PPRHs circumvent off-target effects and are non-immunogenic.</dc:description>
               <dc:date>2021-07-08T10:32:28Z</dc:date>
               <dc:date>2021-07-08T10:32:28Z</dc:date>
               <dc:date>2019-03-26</dc:date>
               <dc:date>2021-07-08T10:32:28Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1002/cpnc.78</dc:relation>
               <dc:relation>Current protocols in nucleic acid chemistry, 2019, vol. 77, num. 1, p. e78</dc:relation>
               <dc:relation>https://doi.org/10.1002/cpnc.78</dc:relation>
               <dc:rights>(c) John Wiley &amp; Sons, 2019</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>John Wiley &amp; Sons</dc:publisher>
               <dc:source>Articles publicats en revistes (Bioquímica i Fisiologia)</dc:source>
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