Details

Targeting G-rich lncRNA and its structural polymorphism with selective G-quadruplex ligands : an NMR study
ID Satta, Giuseppe (Author), ID Brčič, Jasna (Author), ID Plavec, Janez (Author)

.pdfPDF - Presentation file, Download (2,57 MB)
MD5: 6982FE6FF19469C6BC1AA858A58B8385
URLURL - Source URL, Visit https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202502472 This link opens in a new window

Abstract
Long noncoding RNAs (lncRNAs) play essential regulatory roles, often mediated by complex structural elements such as RNA G-quadruplexes (rGQs). While ligand interactions with DNA G-quadruplexes (dGQs) have been extensively studied, for rGQs remain less explored. Here, we studied the SL15P RNA oligonucleotide derived from the REG1CP lncRNA, which adopts a parallel rGQ structure in equilibrium with a hairpin (Hp). A set of 12 small molecules, previously known for their ability to make complex with dGQs, was tested for their ability to bind and stabilize the SL15P rGQ. Using NMR spectroscopy, we analyzed complex formation and assessed whether these ligands could promote rGQ folding under conditions where the Hp structure is favored. Melting experiments with circular dichroism (CD) quantified the thermal stabilization induced by ligand binding. Our results show that ligands known to target dGQs exhibit different behaviors toward rGQs. Among the tested compounds, 360A, PhenDC3, and PDS proved to be the most effective, as they induced well-defined complex formation and significant stabilization of the SL15P rGQ. PhenDC3 showed evidence of a dual binding interaction. This study emphasizes that the binding of ligands to rGQs can be highly variable and supports the rational design of selective compounds for therapeutic purposes.

Language:English
Keywords:G-quadruplex, ligand, IncRNA, NMR spectroscopy
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:10 str.
Numbering:Vol. 31, iss. 72, art. e02472
PID:20.500.12556/RUL-178160 This link opens in a new window
UDC:577
ISSN on article:1521-3765
DOI:10.1002/chem.202502472 This link opens in a new window
COBISS.SI-ID:265260803 This link opens in a new window
Publication date in RUL:20.01.2026
Views:126
Downloads:39
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Chemistry : a European journal
Shortened title:Chemistry
Publisher:Wiley, Chemistry Europe
ISSN:1521-3765
COBISS.SI-ID:21813253 This link opens in a new window

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.

Secondary language

Language:Slovenian
Keywords:biokemija, RNK, G-kvadrupleksi, ligandi

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P1-0242
Name:Kemija in struktura bioloških učinkovin

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J1-60019
Name:Strukture z gvanini bogatih zaporedij nekodirajočih RNA kot regulatorjev izražanja genov

Funder:CERIC-ERIC

Funder:CERIC-ERIC
Acronym:DNANANOCERIC

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back