Exploring Sequence Space to Design Controllable G-Quadruplex Topology Switches

0563710 - BFÚ 2023 RIV CN eng J - Journal Article
Chen, J. - Cheng, M. - Stadlbauer, Petr - Šponer, Jiří - Mergny, Jean-Louis - Ju, H. - Zhou, J.
Exploring Sequence Space to Design Controllable G-Quadruplex Topology Switches.
CCS CHEMISTRY. Roč. 4, č. 9 (2022), s. 3036-3050. E-ISSN 2096-5745
R&D Projects: GA ČR(CZ) GA21-23718S; GA MŠMT EF15_003/0000477
Institutional support: RVO:68081707
Keywords : G-quadruplex * G-quadruplex topology * G-switch * sequence composition * structural versatility
OECD category: Biochemistry and molecular biology
Impact factor: 11.2, year: 2022
Method of publishing: Open access
https://www.chinesechemsoc.org/doi/10.31635/ccschem.021.202101357

As nonclassical nucleic acid structures, G-quadruplexes (G4s) not only play important roles in gene regulation and stability maintenance, but are also widely used in nanotechnology. Structural diversity is one of the main factors explaining the popularity of G4s, but a comprehensive and integrated study of different factors determining G4 structural versatility is currently lacking. Herein, starting from a common G4 sequence, (G3T)3G3, as the parent chain, and then taking advantage of G4 versatility, we present a variety of strategies to control G4 structure, based on the regulation of loop length and flanking sequences, cation (type and concentration), and molecular crowding. These strategies allow us to con-vert the G4 topology from parallel to hybrid, to antiparallel, and then back to parallel. Such structural diversity reveals the coding regulation ability of G4 structures, with potential applications in nanotechnology.
Permanent Link: https://hdl.handle.net/11104/0339366