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Induction of DNA single- and double-strand breaks by excited intra- or extracellular green fluorescent protein
被引:1
|作者:
Harla, Izabela
[1
,2
]
Pawlus, Weronika
[1
]
Zarebski, Miroslaw
[1
]
Dobrucki, Jurek W.
[1
]
机构:
[1] Jagiellonian Univ, Fac Biochem Biophys & Biotechnol, Dept Cell Biophys, Krakow, Poland
[2] Jagiellonian Univ, Doctoral Sch Exact & Nat Sci, Krakow, Poland
关键词:
Green fluorescent protein;
Phototoxicity;
DNA;
DNA single-strand breaks;
DNA double-strand breaks;
Singlet oxygen;
OXIDATIVE STRESS;
VISIBLE-LIGHT;
LIVE CELLS;
DAMAGE;
OXYGEN;
GFP;
PHOTOSENSITIZATION;
PHOSPHORYLATION;
PHOTOTOXICITY;
MICROSCOPY;
D O I:
10.1016/j.jphotobiol.2024.113001
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:
Green fluorescent protein (GFP) has opened vast new avenues in studies of live cells and is generally perceived as a benign, nontoxic and harmless fluorescent tag. We demonstrat that excited GFP is capable of inducing substantial DNA damage in cells expressing fusion proteins. In the presence of GFP, even low doses of blue light (12 mu J) induce single strand breaks (SSBs). When the fluorescence of GFP located in the cell nucleus or in the cytoplasm is excited by a much higher dose (17 mJ), DNA double-strand breaks (DSBs) are also induced. Such breaks are induced even when GFP is placed and illuminated in culture medium outside of living cells. We demonstrate that DNA damage is induced by singlet oxygen, which is generated by excited GFP. Although short exposures of live cells to exciting light typically used in fluorescence microscopy induce SSBs but carry little risk of inducing DNA double-strand breaks, larger doses, which may be used in FRAP, FLIM, FCS and super-resolution fluorescence microscopy studies, are capable of inducing not only numerous SSBs but also DSBs.
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