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UV-Induced Adenine Radicals Induced in DNA A-Tracts: Spectral and Dynamical Characterization
被引:35
|作者:
Banyasz, Akos
[1
]
Ketola, Tiia-Maaria
[1
,4
]
Munoz-Losa, Aurora
[1
,5
]
Rishi, Sunny
[2
]
Adhikary, Amitava
[2
]
Sevilla, Michael D.
[2
]
Martinez-Fernandez, Lara
[3
]
Improta, Roberto
[3
]
Markovitsi, Dimitra
[1
]
机构:
[1] Univ Paris Saclay, CNRS, CEA, LIDYL, F-91191 Gif Sur Yvette, France
[2] Oakland Univ, Dept Chem, Rochester, MI 48309 USA
[3] CNR, Ist Biostrutture & Bioimmagini, Via Mezzocannone 16, I-80134 Naples, Italy
[4] CP Kelco Oy, Kuhnamontie 2,PL 500, FI-44101 Aanekoski, Finland
[5] Univ Vienna, Inst Theoret Chem, Wahringer Str 17, A-1090 Vienna, Austria
来源:
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
|
2016年
/
7卷
/
19期
基金:
美国国家卫生研究院;
关键词:
ONE-ELECTRON OXIDATION;
AQUEOUS-SOLUTION;
CATION DEPROTONATION;
FLASH-PHOTOLYSIS;
LASER PHOTOLYSIS;
BASE STACKING;
IONIZATION;
DAMAGE;
PURINE;
PHOTOEXCITATION;
D O I:
10.1021/acs.jpclett.6b01831
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Adenyl radicals generated in DNA single and double strands, (dA)(20) and (dA)(20)center dot(dT)(20), by one- and two-photon ionization by 266 nm laser pulses decay at 600 nm with half-times of 1.0 +/- 0.1 and 4 +/- 1 ms, respectively. Though ionization initially forms the cation radical, the radicals detected for (dA)(20) are quantitatively identified as N6-deprotonated adenyl radicals by their absorption spectrum, which is computed quantum mechanically employing TD-DFT. Theoretical calculations show that deprotonation of the cation radical induces only weak spectral changes, in line with the spectra of the adenyl radical cation and the deprotonated radical trapped in low temperature glasses.
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页码:3949 / 3953
页数:5
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