4.2 Article

Exploring Sequence Space to Design Controllable G-Quadruplex Topology Switches

Journal

CCS CHEMISTRY
Volume 4, Issue 9, Pages 3036-3050

Publisher

CHINESE CHEMICAL SOC
DOI: 10.31635/ccschem.021.202101357

Keywords

G-quadruplex; G-quadruplex topology; G-switch; sequence composition; structural versatility

Funding

  1. National Natural Science Foundation of China [21977045, 21635005]
  2. Fundamental Research Funds for the Central Universities [02051430210]
  3. Nanjing University [020514912216]
  4. Czech Science Foundation [21- 23718S]
  5. project SYMBIT - ERDF [CZ.02.1.01/0.0/0.0/15_003/0000477]

Ask authors/readers for more resources

G-quadruplexes (G4s) are nonclassical nucleic acid structures that play important roles in gene regulation and stability maintenance, and are widely used in nanotechnology. However, a comprehensive study of the factors determining G4 structural versatility is currently lacking.
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. [GRAPHICS] .

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