1. Introduction
Cancer remains one of the most deadly diseases for humans and therefore attempts are always being made to improve the methods of treatment for cancer. One of the most recent developments is hadron therapy, which is the use of charged particles to destroy cancer-infected cells [
1,
2]. Hadron therapy uses protons or C
6+ as the charged particle to damage the molecules in the cells. Statistically when targeting cancer cells with beams of cations it is most likely for the ions to collide with water molecules and generate different radicals. One of these radicals that can be formed is the OH-radical, which can then react with other molecules in the cell such as DNA [
3].
Multiple other reactions are also possible and therefore detailed knowledge of the chemical reactions and their reaction mechanisms that lead to DNA damage is of great importance as one strives to improve the selectivity of the radiation treatment in order to reduce the side effects. Currently, it has only been possible to experimentally determine the total rate constants for each DNA nucleobase [
4]; therefore, computational efforts are required to further investigate the exact reaction mechanisms.
Previous computational studies (for a more extended review of the literature, see, e.g., [
5]) have indicated that the OH-radicals that are formed react with the DNA nucleobases by either abstraction of a hydrogen or by addition to the aromatic rings in the nucleobase [
6]. Density functional theory (DFT) calculations showed that addition reactions are more favored than abstraction reactions for uracil [
7], while others have shown that the same is the case for guanine [
8]. Previously published results from calculations of reactions kinetics in the gas phase by our group also showed that both the addition and abstraction pathways are important for the total rate constant in DNA nucleobases [
5,
9]. Meanwhile, experimental results have shown that hydrogen abstraction also happens from the ribofuranose part of nucleosides [
10,
11]. This is one of the reasons for extending our calculations [
5,
9,
12,
13] to cover in this work nucleosides instead of just nucleobases. Nucleosides contain the respective nucleobase bound to a ribofuranose molecule and calculations on these molecules will therefore give a better picture concerning what happens in actual DNA, as DNA consists of nucleosides and phosphate groups [
14].
In this context, it should be mentioned that this work does not take any solvent effects into account, partly as we want to be able to compare our new results for the nucleotides directly to the results of the previous gas phase study for the nucleobases [
5,
9]. Solvent effects are of course potentially important in the context of actual DNA in the human body. Solvation has previously been shown to increase the barrier for hydrogen abstraction reactions and make the LUMO orbitals of the nucleobases more compact [
8]. Solvent effects were also investigated within our group for reactions with adenine and those results indicated that solvation does have an effect on the rate constants and energetics, but it did not really change the preference of the reaction pathways [
12]. However, it was also observed that the standard approach for treating solvation, i.e., the PCM model, did not improve agreement with experimental values and gave results in contrast to explicitly including solvent molecules in the calculation with or without a surrounding PCM environment. Multiple other studies have considered solvent effects on these types of reactions including another one from our group [
13], where the solvent effects of water on the reaction between the OH-radical and thymine was studied using again not only the PCM model but also inclusion of one or two explicit water molecules. Similar to our investigation of adenine [
12], the different solvent models lead to opposing conclusions. Other studies of solvent effects have been carried out for guanosine and uridine and their nucleobases [
8,
15,
16]. In the present work, however, solvent effects have not been included, because based on our previous studies [
12,
13] it is not clear, what a sufficiently accurate model for treating solvation would be. Furthermore, experimental studies [
10] indicate that for duplex DNA in water the accessible surface area of the hydrogen atoms has an important effect, which none of these solvation models can describe. The focus of this work is instead on extending our previous gas phase studies of the nucleobases by studying with the identical computational protocol the possible hydrogen abstraction reactions that the OH-radicals can initiate with two specific nucleosides in contrast to their respective nucleobases.
Nucleosides consist of two parts, their nucleobase part and then a ribofuranose (RF) part. The nucleosides chosen in this work are guanosine and uridine, which contain the two nucleobases guanine and uracil—a purine and a pyrimidine type nucleobase. The motivation for choosing these nucleosides is that guanine is the largest of the DNA nucleobases while uracil is the smallest and that we cover with them both purine and pyrimidine nucleobases.
The separation in a nucleobase and ribofuranoce part can also be seen in the chosen labelling of the hydrogens in
Figure 1, as two different labelling schemes have been used for the different parts of the nucleosides. In the RF part the hydrogens have been labelled according to which atom they are bound to.
In this project OH-radical hydrogen abstraction reactions were investigated on all but one of the hydrogens in each molecule. The last hydrogens, O5, are replaced by phosphate groups in the actual DNA in a human body and were therefore not investigated, although they were present in the calculations for the other hydrogens. Furthermore, the OH-radical addition reactions to the double bonds in the nucleobases will not be investigated here again.
The aim of the project is to calculate thermodynamic properties of these hydrogen abstraction reactions, calculate the rate constants and then compare them with the results of the previous studies [
9,
12]. These previous studies investigated all five nucleobases, where the two that are interesting for this study are of course guanine and uracil. In order to accurately compare the results from this study to the previous ones, the computational methods have to be identical. Therefore, the rate constants will be calculated with transition state theory with an Eckart tunneling correction.
The initial intention behind this study was to investigate a couple of different things, one of them being how large the difference between just having the nucleobase in the calculations and also including the ribofuranose molecule is for different properties. This could give a better picture of how accurate all calculations done on just nucleobases are for actual DNA. On top of that, it is interesting, if there is a difference in the properties of ribofuranose, whether it is bound to different nucleobases, which in this case would be guanine and uracil. This might make it possible to predict how ribofuranose will behave when bound to other nucleobases without necessarily running the same amount of calculations.
2. Results and Discussion
The standard reaction Gibbs free energies, , of all hydrogen abstractions were calculated as difference between the standard Gibbs free energies of the products and reactions. Correspondingly, the difference in standard Gibbs free energies between the transition state and the reactants, , was obtained.
Figure 2 and
Figure 3 show the change in Gibbs free energy. All of the free energies presented in the plots are relative to the free energy of the reactants, which makes all the reactions for each respective molecule start at the value of 0 kJ/mol, as the starting point of each reaction is the same, namely the free Gibbs energy of an OH-radical and either guanosine or uridine added together.
The four other points on the plots are the reactant complex, the transition state, the product complex, and the products. From these figures it becomes clear that in both nucleosides the reactions of the hydrogens bound to carbons in the ribofuranose part are very similar in energy, whereas the reactions in the nucleobase part are very different for the two nucleosides, which is to be expected. In
Figure 4 and
Figure 5, the RF and the nucleobase part are therefore separated into different plots.
Separating the different parts of uridine makes it very clear that the different hydrogen reactions for uridine can be put into three groups regarding the Gibbs free energy. With those three being the ribofuranose hydrogens bound to carbons, ribofuranose hydrogens bound to oxygens and finally the hydrogens bound to the nucleobase. The data indicate that the ribofuranose hydrogens bound to carbons will have the largest reaction rates and be the most thermodynamically stable given that the values are the smallest and the values the most negative ones for that group.
For guanosine, the two groups that have to do with RF follow the same trend as for uridine. As for the nucleobase part, it is a bit more complicated as one of the nucleobase hydrogens behaves completely differently from the other three as discussed previously [
9]. The former three are very similar to the hydrogens bound to the RF part of guanosine, while the H8 reaction is similar to the nucleobase reactions in uridine. However, one would expect from
Figure 4 and
Figure 5 that the hydrogen abstraction reactions for guanosine will have more similar rate constants than the uridine reactions.
2.1. Gibbs Free Energies: and
Looking at the exact values of the Gibbs free energies presented in
Table 1, one can attempt to predict the relative sizes of the rate constants by looking at the relative
values. For guanosine, these values are very similar for all reactions except for the H8 hydrogen. The H8 reaction has a higher
which should result in the rate constant being smaller than for the rest of the guanosine reactions. As for uridine, the hydrogens bound to carbons in the RF part have similar values as for the guanosine reactions. The other two groups, which were recognized from the plots, both have higher values for
. The hydrogens bound to oxygens in the RF part and the H5 and H6 hydrogens have around the same values. This should mean that these reactions will have roughly the same rate constant, which should be significantly lower than for the hydrogens bound to carbons in the RF part.
The value of
indicates how thermodynamically stable the product is compared to the reactants. Recalling that the product is a radical and a water molecule, one would expect that the radical would no matter the value of
be very unstable and quickly react with something different in the cell. Nevertheless, we can compare to the results of a recent
B97XD/6-31++G** calculation using the PCM model for solvation [
17]. The trend in their
for the radicals should be comparable to the trend in our reaction Gibbs free energies
. They find a decreasing stability in the radicals C4’ > C1’ > C5’ > C3’ > C2’, while we find C1’ > C2’ > C5’> C4’ > C3’ for guanosine. However, the computational protocols employed in the two calculations differ not only because they used a PCM environment while our calculations are for the gas phase, but more important our basis set is significantly larger, being both a triple zeta basis set and including also second polarization functions on all atoms.
2.2. Eckart Correction
Before comparing the rate constants, the relative size of the Eckart tunneling corrections in
Table 2 will be discussed. The Eckart tunneling correction includes contributions from the forward and the reverse energy barriers, calculated from the zero-point vibrationally corrected energies. The Eckart corrections were calculated via an in-house unpublished program, which calculates the integral numerically.
Looking at the values of the Eckart corrections, a similar pattern as with the thermodynamic data can be observed. In both molecules, all of the hydrogens bound to carbons in the RF part have Eckart correction values of around 1. As for the other reactions, they mostly have values that are significantly larger than 1, which in some cases makes sense when looking at just the forward and reverse energy barriers. This can explain the higher values of the Eckart correction because having a higher forward energy barrier allows for more possibilities for tunneling, while having a lower reverse energy barrier allows for fewer possibilities for the “reverse” tunneling. However, one should keep in mind that this correction only accounts for the tunneling effects, meaning that a larger tunneling correction could be associated with an otherwise less favorable reaction.
In some reactions, just looking at the forward and reverse barriers is not enough to explain the relative value of the Eckart corrections compared to some of the other reactions, such as, e.g., for the O2 and O3 reactions in guanosine, which have values of 15.05 and 14.26, respectively. They have basically the same forward energy barrier but there is a significant difference in the reverse energy barrier. This means that one cannot just look at the energy barriers and conclude the value of the Eckart correction from that alone, as it also depends on other properties such as the value of the zero-point vibrationally corrected energies, which are very similar in this case.
2.3. Rate Constants
In
Table 3, we finally present the rate constants calculated for the abstraction of the different hydrogen atoms in guanosine and uridine. The results show that reaction at C4’, i.e., in the RF part of the nucleoside, has the largest rate constant for both molecules at
and
for guanosine and uridine, respectively, followed by the abstraction of a hydrogen from C2’—again in the RF part. When looking at the other calculated properties, one observes that these reactions have also the lowest
values for both molecules. This inverse relationship between the rate constant and
can be noticed throughout all of the reactions, showing that the energy term in the TST equation for the rate constant, Equation (
1), is the dominant term.
From
Figure 4, one would expect that the reactions of the hydrogens bound to carbons in the RF part of the molecules would have rate constants that are larger than the hydrogens bound to the oxygens in the RF and the nucleobase part of uridine. From
Figure 5, one would instead expect there to be more parity between the different hydrogen abstraction reactions’ rate constants with the exception of the H8 reaction. Both of these expectations turn out to be true when looking at the data in
Table 3.
These data imply that the abstraction reactions of two of the hydrogens in the RF part of guanosine and of all the hydrogens bound to carbon in the RF part of uridine are faster and thus more important than the hydrogen abstraction reactions in the corresponding nucleobases. Compared to the fastest OH-radical addition reactions in guanine and uracil with rate constants
for guanine and
for uracil [
9], these hydrogen abstraction reactions in the RF part of the nucleosides are also clearly competitive.
Another thing to note when comparing the rate constants, is the difference in size of the rate constants belonging to the hydrogen abstraction reactions in the nucleobase parts of the two molecules. For uridine, the rate constants belonging to the hydrogens in the uracil part are negligible compared to the reactions in the RF part. For guanosine, on the other hand, those rate constants are more significant with three of them, for H1, H21 and H22, being just one order of magnitude smaller than the largest rate constant for the whole nucleoside.
We can also compare, in
Table 4 and
Table 5, our rate constants for the hydrogen abstraction reactions in the nucleobase part of the nucleosides to the previous results for the hydrogen abstraction reactions in the nucleobases themselves [
9]. In general, the changes in the rate constants due to the RF part are relatively small. With the exception of the abstraction of H6 in uracil/uridine, which changes by approximately a factor 40, they differ by less than one order of magnitude. For most of the hydrogens, the rate constants are larger in the nucleosides. The exceptions are H21 in guanosine and H5 in uridine.
Based on the result for these to protypical purine and pyrimidine nucleosides, we predict that the rate constants for the hydrogen abstraction reactions in the other three nucleobases, adenine, cytosine and thymine, will also be rather independent of whether or not the nucleobase is a standalone molecule or if it is bound to an RF molecule. The rate constants of nucleobase hydrogen abstraction in the rest of the nucleosides is thus expected to be within an order of magnitude from the results of the previous studies on the nucleobases [
9].
We can also compare our results in
Table 3 with experimental results obtained for duplex DNA in water [
10]. They observed an order of reactivity H5’ > H4’ > H3’ ≈ H2’ ≈ H1’ and could show that it is directly correlated to the solvent-accessible surface area of the hydrogens—an effect which is not included in our calculations. Our results are, in contrast, for the intrinsic reaction kinetics, which consequently can not easily be extracted from experimental data.
Although no research was carried out on the OH-radical addition reactions in the nucleoase part of the nucleosides, and therefore it is unknown whether the rate constants will be higher or lower for those reactions in guanosine and uridine than in guanine and uracil, those rate constants are not expected to be significantly different from the largest one of the hydrogen abstraction reactions. Which means that it is very likely that these OH-radical addition reactions will compete with the C4’ hydrogen abstraction reaction in both guanosine and uridine.
4. Conclusions
We have systematically investigated all hydrogen abstraction reactions in the two nucleosides guanosine and uridine with DFT calculations at the B97X-D/6-311G++(2df,2pd) level. The investigation has shown that in general the most favorable hydrogen abstraction reactions occurs on the carbon-bound hydrogens in the ribofuranose part of the nucleosides and not in the nucleobase part. The fastest hydrogen abstraction reaction is the one that occurs on the C4’ hydrogen, with a rate constant of for guanosine and for uridine. These two reactions also have the lowest , indicating that the rate constants are dominated by the exponential energy term.
Comparisons made between the results from the nucleobases alone [
9], and from the results gathered in this work on the nucleobases in the nucleoside environment, show that the rate constants for those hydrogen abstraction reactions can be mostly considered as independent of whether or not the nucleobase is a standalone molecule.
Comparing the rate constants of the hydrogen abstractions in the nucleosides with the rate constants for the OH-radical addition reactions to the nucleobases shows that they are of the same order of magnitude and thus both important, supporting thus the previous findings for the nucleobases alone [
9].
Further calculations including the phosphate groups, that are bound to guanosine and uridine instead of the O5 hydrogen, could be attempted in future work, although that might require sacrificing some accuracy in the computational method in order to reduce the computational cost. Another possibility for future work would be to investigate how much the rate constants of the OH-radical addition reactions in guanosine and uridine are actually affected by the RF part.