Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Repository of the University of Ljubljana
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Advanced
New in RUL
About RUL
In numbers
Help
Sign in
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
)
PDF - Presentation file,
Download
(2,57 MB)
MD5: 6982FE6FF19469C6BC1AA858A58B8385
URL - Source URL, Visit
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202502472
Image galllery
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
UDC:
577
ISSN on article:
1521-3765
DOI:
10.1002/chem.202502472
COBISS.SI-ID:
265260803
Publication date in RUL:
20.01.2026
Views:
126
Downloads:
39
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
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
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