Single-molecule localization microscopy as a promising tool for gamma H2AX/53BP1 foci exploration

Investor logo

Warning

This publication doesn't include Faculty of Arts. It includes Faculty of Science. Official publication website can be found on muni.cz.
Authors

DEPEŠ Daniel LEE Jin-Ho BOBKOVA Elizaveta JEZKOVA Lucie FALKOVA Iva BESTVATER Felix PAGACOVA Eva KOPECNA Olga ZADNEPRIANETC Mariia BACIKOVA Alena KULIKOVA Elena SMIRNOVA Elena BULANOVA Tatiana BOREYKO Alla KRASAVIN Evgeny HAUSMANN Michael FALK Martin

Year of publication 2018
Type Article in Periodical
Magazine / Source The European Physical Journal D
MU Faculty or unit

Faculty of Science

Citation
Web Full Text
Doi http://dx.doi.org/10.1140/epjd/e2018-90148-1
Keywords DOUBLE-STRAND BREAKS; COMPLEX CELL RESPONSES; CLUSTERED DNA-DAMAGE; HIGH-LET IRRADIATION; NANOSCOPY TECHNIQUES; ELECTRON-MICROSCOPY; CHROMATIN-STRUCTURE; MULTISCALE APPROACH; RADIATION-DAMAGE; REPAIR
Description Quantification and structural studies of DNA double strand breaks (DSBs) are an essential part of radiobiology because DSBs represent the most serious damage introduced to the DNA molecule by ionizing radiation. Although standard immunofluorescence confocal microscopy has demonstrated its usefulness in a large number of research studies, it lacks the resolution required to separate individual, closely associated DSBs, which appear after cell exposure to high linear energy transfer (high-LET) radiation and can be visualized as clusters or streaks of radiation-induced repair foci (IRIFs). This prevents our deeper understanding of DSB induction and repair. Recent breakthroughs in super-resolution light microscopy, such as the development of single-molecule localization microscopy (SMLM), offer an optical resolution of approximately an order of magnitude better than that of standard confocal microscopy and open new horizons in radiobiological research. Unlike electron microscopy, SMLM (also referred to as "nanoscopy") preserves the natural structure of biological samples and is not limited to very thin sample slices. Importantly, SMLM not only offers a resolution on the order of approximately 10 nm, but it also provides entirely new information on the biochemistry and spatio-temporal organization of DSBs and DSB repair at the molecular level. Nevertheless, it is still challenging to correctly interpret these often surprising nanoscopy results. In the present article, we describe our first attempts to use SMLM to explore gamma H2AX and 53BP1 repair foci induced with( 15) N high-LET particles.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.