Hindered intermolecular stacking of anti-parallel telomeric G-quadruplexes

Telomeric G-quadruplexes (G4s) are non-canonical DNA structures composed of TTAGGG repeats. They are extensively studied both as biomolecules key for genome stability and as promising building blocks and functional elements in synthetic biology and nanotechnology. This is why it is extremely important to understand how the interaction between G4s is affected by their topology. We used small-angle x-ray scattering to investigate the end-to-end stacking of antiparallel telomeric G-quadruplexes formed by the sequence AG3(T2AG3)3. To represent the experimental data, we developed a highly efficient coarse-grained fitting tool, which successfully described the samples as an equilibrium mixture of monomeric and dimeric G4 species. Our findings indicate that the antiparallel topology prevents the formation of long multimeric structures under self-crowding conditions, unlike the hybrid/parallel structures formed by the same DNA sequence. This result supports the idea that the stacking of monomeric G-quadruplexes is strongly affected by the presence of diagonal loops.

Authors

Institutions

Publication Details

Journal
The Journal of Chemical Physics
Published
2024-09-09
DOI
https://doi.org/10.1063/5.0225371
Citations
1
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
0.23

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Hindered intermolecular stacking of anti-parallel telomeric G-quadruplexes

Sara Catalini, Valeria Libera, C. Petrillo, Luca Bertini et al.
1 citations
The Journal of Chemical Physics
DNA and Nucleic Acid Chemistry
0.23
article

Hindered intermolecular stacking of anti-parallel telomeric G-quadruplexes

Sara Catalini, Valeria Libera, C. Petrillo, Luca Bertini, A. Orecchini, Cristiano De Michele, Alessandro Paciaroni, Bruno Pagano, Lucia Comez, Giorgio Schirò, Renzo Campanella, Valentina Arciuolo
article en
1 citations

Abstract

Telomeric G-quadruplexes (G4s) are non-canonical DNA structures composed of TTAGGG repeats. They are extensively studied both as biomolecules key for genome stability and as promising building blocks and functional elements in synthetic biology and nanotechnology. This is why it is extremely important to understand how the interaction between G4s is affected by their topology. We used small-angle x-ray scattering to investigate the end-to-end stacking of antiparallel telomeric G-quadruplexes formed by the sequence AG3(T2AG3)3. To represent the experimental data, we developed a highly efficient coarse-grained fitting tool, which successfully described the samples as an equilibrium mixture of monomeric and dimeric G4 species. Our findings indicate that the antiparallel topology prevents the formation of long multimeric structures under self-crowding conditions, unlike the hybrid/parallel structures formed by the same DNA sequence. This result supports the idea that the stacking of monomeric G-quadruplexes is strongly affected by the presence of diagonal loops.

The Journal of Chemical PhysicsVol. 161(10)
Centre National de la Recherche Scientifique (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), University of Perugia (IT), CEA Grenoble (FR), Institut de Biologie Structurale (FR), University of Naples Federico II (IT), Sapienza University of Rome (IT), Université Grenoble Alpes (FR)
European Commission, European Synchrotron Radiation Facility, Università degli Studi di Perugia, Ministero dell'Università e della Ricerca
Openalex Percentile: Top 43%
DNA and Nucleic Acid Chemistry
0.23
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.