AI Article Synopsis

  • Research explored the effects of different length disulfide (S-S) linkers on RNA hairpins, specifically using dimethylene (DME), diethylene (DEE), and dipropylene (DPE) linkers.
  • Synthesis of modified uridine phosphoramidites allowed for the incorporation of these linkers into RNA sequences, with thermal analysis revealing that DEE and DPE linkers destabilize RNA duplexes while maintaining hairpin structure.
  • Results showed that DME and DEE linkers enhance hairpin locking, while DPE offers more conformational flexibility, indicating the utility of S-S linkers in studying RNA interactions.

Article Abstract

We recently reported the properties of RNA hairpins constrained by a dimethylene (DME) disulfide (S-S) linker incorporated between two adjacent nucleosides in the loop and showed that this linker locked the hairpin conformation thus disturbing the duplex/hairpin equilibrium. We have now investigated the influence of the length of the linker and synthesized oligoribonucleotides containing diethylene (DEE) and dipropylene (DPE) S-S bridges. This was achieved via the preparation of building blocks, namely 2'-O-acetylthioethyl (2'-O-AcSE) and 2'-O-acetylthiopropyl (2'-O-AcSP) uridine phosphoramidites, which were successfully incorporated into RNA sequences. Thermal denaturation analysis revealed that the DEE and DPE disulfide bridges destabilize RNA duplexes but do not disrupt the hairpin conformation. Furthermore, our investigation of the duplex/hairpin equilibrium indicated that sequences modified with DME and DEE S-S linkers predominantly lock the hairpin form, whereas the DPE S-S linker provides flexibility. These findings highlight the potential of S-S linkers to study RNA interactions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11319213PMC
http://dx.doi.org/10.1002/open.202300232DOI Listing

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