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Structural changes in plasmid DNA caused by radiation and its protection by Ectoine: an AFM analysis
(2017)
Most ionizing radiation in water ends in an avalanche of low energy electrons which play a dominant role together with OH-radicals in damaging DNA. In the present study we irradiated plasmid DNA with electrons (primary energy 30keV) under physiological conditions, performed with as well as without Ectoine. Ectoine is a compatible solute, synthesized and accumulated in molar concentration within bacteria to withstand osmotic stress or different other stressors.
Plasmid DNA (pUC19, 2686 bp) was studied due to its supercoiled isoform which is highly sensitive to radiation damage. In biochemistry gel electrophoresis is applied for structural analysis of DNA. Although it is a standard technique, a reliable discrimination of short fragments caused by radiation is often difficult. AFM is also commonly used for imaging susceptible biomolecules and, since it is based on a single molecule observation, for analysis of contour lengths of linear DNA as well. Therefore, in our study the structural changes in plasmid DNA after irradiation with different doses were quantitatively analyzed by means of intermittent contact AFM. The figure shows representative AFM images of electron irradiated pUC19 DNA (bar=200nm). For AFM imaging the DNA was chemically fixed on ultra-smooth mica. As can be clearly seen, with increasing radiation dose the number of undamaged DNA declines and fragmented DNA arises (A, B). In aqueous Ectoine solution (1M) the effect of radiation on DNA is dramatically depressed. Ectoine apparently confers protection even against high radiation: the plasmids remain predominantly in the supercoiled isoform (D). Therefore, we strongly believe that Ectoine is a potent protective substance of DNA against ionizing radiation.
In dosimetry the determination of the effectiveness of the damaging processes is standardized and accounted for by the radiation and tissue weighting factor. For the underlying constituents of the tissue, that is the various biomolecules, such a systematic approach doesn't exist. This makes it difficult to compare results obtained under different experimental conditions. In the following work, we will describe a method to obtain comparable values for the radiation-biomolecule interaction, measured under different conditions. This approach can lead to standardization of dosedamage relationship at the molecular level. Such approach is necessary for a better understanding of the relations between the damage of the single constituents of biological tissue and the whole – finally gaining a more complete picture of irradiation damage.
Tapping mode AFM (TM-AFM) is a standard technique to image biomolecules and cells avoiding damage to susceptible samples.
For preparing AFM samples we fixed (untreated and radiated) plasmids chemically on ultra-smooth mica silanized with APTES.
The recorded AFM images were examined concerning the contour length, the conformation and the writhing number of the plasmids.
We found that the measured contour length is in accordance with the number of base pairs. Apart from that, we indicate different structures of plasmids from our AFM images, which were assigned to our plasmid data from agarose gel-electrophoresis.
We use a dynamic scanning electron microscope (DySEM) to analyze the movement of oscillating micromechanical structures. A dynamic secondary electron (SE) signal is recorded and correlated to the oscillatory excitation of scanning force microscope (SFM) cantilever by means of lock-in amplifiers. We show, how the relative phase of the oscillations modulate the resulting real part and phase pictures of the DySEM mapping. This can be used to obtain information about the underlying oscillatory dynamics. We apply the theory to the case of a cantilever in oscillation, driven at different flexural and torsional resonance modes. This is an extension of a recent work (Schr¨oter et al 2012 Nanotechnology 23 435501), where we
reported on a general methodology to distinguish nonlinear features caused by the Imaging process from those caused by cantilever motion.
Analytical and numerical analysis of imaging mechanism of dynamic scanning electron microscopy
(2012)
The direct observation of small oscillating structures with the help of a scanning electron beam is a new approach to study the vibrational dynamics of cantilevers and microelectromechanical systems. In the scanning electron microscope, the conventional signal of secondary electrons (SE, dc part) is separated from the signal response of the SE detector, which is correlated to the respective excitation frequency for vibration by means of a lock-in amplifier. The dynamic response is separated either into images of amplitude and phase shift or into real and imaginary parts. Spatial resolution is limited to the diameter of the electron beam. The sensitivity limit to vibrational motion is estimated to be sub-nanometer for high integration times. Due to complex imaging mechanisms, a theoretical model was developed for the interpretation of the obtained measurements, relating cantilever shapes to interaction processes consisting of incident electron beam, electron–lever interaction, emitted electrons and detector response. Conclusions drawn from this new model are compared with numerical results based on the Euler–Bernoulli equation.
A specially designed scanning force microscope (SFM, atomic force microscope – AFM) was incorporated into the chamber of a commercial scanning electron microscope (SEM) to investigate vibrating SFM cantilevers at their resonance. Inherently, the spatial resolution of electron microscopy is higher than that of optical methods. In this paper we present vibration modes (eigenmodes) of two different SFM cantilevers. Their nonlinear behavior is also explored in order to depict their 2nd harmonics (twice the fundamental frequency). Imaging of the local vibration is performed by measuring the frequency- and phase-selective responses of the SE signal at different X and Y positions of the scanned electron beam.