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G-Quadruplex Targeting in the Fight against Viruses: An Update
被引:57
|作者:
Ruggiero, Emanuela
[1
]
Zanin, Irene
[1
]
Terreri, Marianna
[1
]
Richter, Sara N.
[1
]
机构:
[1] Univ Padua, Dept Mol Med, I-35121 Padua, Italy
关键词:
G-quadruplexes;
virus;
targeting;
G-quadruplex ligands;
antiviral therapy;
CATIONIC PORPHYRIN TMPYP4;
TELOMERIC G-QUADRUPLEX;
RNA-POLYMERASE I;
FORMING SEQUENCES;
INTERACTIVE AGENTS;
PROMOTER REGION;
NUCLEAR ANTIGEN;
IMMUNE EVASION;
SMALL-MOLECULE;
UNIQUE DOMAIN;
D O I:
10.3390/ijms222010984
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
G-quadruplexes (G4s) are noncanonical nucleic acid structures involved in the regulation of key cellular processes, such as transcription and replication. Since their discovery, G4s have been mainly investigated for their role in cancer and as targets in anticancer therapy. More recently, exploration of the presence and role of G4s in viral genomes has led to the discovery of G4-regulated key viral pathways. In this context, employment of selective G4 ligands has helped to understand the complexity of G4-mediated mechanisms in the viral life cycle, and highlighted the possibility to target viral G4s as an emerging antiviral approach. Research in this field is growing at a fast pace, providing increasing evidence of the antiviral activity of old and new G4 ligands. This review aims to provide a punctual update on the literature on G4 ligands exploited in virology. Different classes of G4 binders are described, with emphasis on possible antiviral applications in emerging diseases, such as the current COVID-19 pandemic. Strengths and weaknesses of G4 targeting in viruses are discussed.
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