Different Mechanisms of DNA Radiosensitization by 8-Bromoadenosine and 2 '-Deoxy-2 '-fluorocytidine Observed on DNA Origami Nanoframe Supports

0558117 - ÚFCH JH 2023 RIV US eng J - Článek v odborném periodiku
Sala, Leo Albert - Lyshchuk, Hlib - Šáchová, Jana - Chvátil, David - Kočišek, Jaroslav
Different Mechanisms of DNA Radiosensitization by 8-Bromoadenosine and 2 '-Deoxy-2 '-fluorocytidine Observed on DNA Origami Nanoframe Supports.
Journal of Physical Chemistry Letters. Roč. 13, č. 17 (2022), s. 3922-3928. ISSN 1948-7185
Grant CEP: GA ČR(CZ) GX21-26601X; GA MŠMT EF16_026/0008382; GA MŠMT(CZ) EF16_019/0000785
Grant ostatní: Ministerstvo školství, mládeže a tělovýchovy(CZ) CZ.02.1.01/0.0/0.0/16_019/0000785; Ministerstvo školství, mládeže a tělovýchovy - GA MŠk(CZ) CZ.02.1.01/0.0/0.0/16_026/0008382
Institucionální podpora: RVO:61388955 ; RVO:68378050 ; RVO:61389005
Klíčová slova: strand breaks * damage * radiation * electrons * sequence
Obor OECD: Physical chemistry; Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect) (UJF-V); Biochemistry and molecular biology (UMG-J)
Impakt faktor: 5.7, rok: 2022
Způsob publikování: Omezený přístup
https://pubs.acs.org/doi/10.1021/acs.jpclett.2c00584

DNA origami nanoframes with two parallel DNA sequences are used to evaluate the effect of nucleoside substituents on radiation-induced DNA damage. Double strand breaks (DSB) of DNA are counted using atomic force microscopy (AFM), and total number of lesions is evaluated using real-time polymerase chain reaction (RT-PCR). Enhanced AT or GC content does not increase the number of DNA strand breaks. Incorporation of 8-bromoadenosine results in the highest enhancement in total number of lesions. However, the highest enhancement in DSB is observed for 2´-deoxy-2´-fluorocytidine, indicating different mechanisms of radiosensitization by nucleoside analogues with the halogen substituent on base or sugar moieties, respectively. ´´Bystander´´ effects are observed, when the number of DSB in a sequence is enhanced by a substituent in the parallel DNA sequence. The present approach eliminates limitations of previously developed methods and motivates detailed studies of poorly understood conformation or bystander effects in radiation induced damage to DNA.
Trvalý link: http://hdl.handle.net/11104/0331920