Difference between revisions of "Team:Heidelberg/Modeling/aptakinetics"

In our project, several parts are based on the prediction of optimal aptamers for binding target molecules and for designing nucleotide stems in switchable AptaBodies that can sense their targets by creating peroxidase activity based on molecular dynamics simulations. To test predictions of optimal aptamers and nucleotide stems, we had developed a high-throughput method for quickly screening the function and the dose-response of switchable AptaBodies. In 96-wells, powers of ten in concentrations of target ligands are tested if they can accelerate the catalysis of luminol, which is detected by a luminescence camera. Here, we use the decay curves of the luminol signal to assess the function of switchable AptaBodies. In its switched-off state, a functional AptaBody does accelerate the luminol catalysis. Whereas, in its on-state, binding of the target changes the conformation of the hemin-binding quadruplex.  This facilitates the binding of hemin, increases the peroxidase activity and therefore accelerates the catalysis of luminol, which is visible by an accelerated decay of the signal.

Assuming an excess of $H_2O_3$ over luminol, the catalysis depends on the concentration of luminol reagent $R$ and the concentration of active enzymes. A low binding affinity of hemin $H$ to the unligated AptaBody $D$ leads to a certain concentration of hemin-bound DNA-AptaBodies $D_H$. In contrast, after binding to the ligand $L$, AptaBodies $D_{LH}$ are supposed to have a stronger affinity for hemin. Because both forms catalyse the luminol reaction, its time-dependent concentration change can be described by the equation:

$\frac{d[R]}{dt}=-k_{cat}[R](D_{H}+D_{LH}), $

in which $k_{cat}$ is the kinetic parameter for the catalysis. This equation can be solved to

$[R](t)=[R](t_{0})\exp\left(-k_{cat}(D_{H}+D_{LH})t\right)$.

Because we are interested in the enzyme activities, this facilitates an elegant way of parameter estimations. Instead of fitting to time series of experimental data, which can be affected by noise and background signal, we only need to extract the decay constant of the signals. For this purpose, we fitted exponential functions: $f(t)=a+exp(-bt)$ to the fluorescence signals from the AptaBody screening experiments and calculated enzyme activities.

$b=k_{cat}(D_{H}+D_{LH})$, and half-lives of the signal $t_{\frac{1}{2}}= \frac{ln2}{b}=\frac{\ln2}{k_{cat}(D_{H}+D_{LH})}$.

These enzyme activities were used for parameter estimations. In the following, the mathematical model shall be described.

Figure 1. Ligand concentration-dependent reporter signal half-lives. (A) For functional aptamer sensor candidates, the luminescence half-life was decreased with increasing ligand concentration (green trajectory) but not altered if the stem was too weak (red trajectory). (B) Model reactions describing binding of hemin H and target ligands L to the DNA-aptamer sensor D and catalysis of the detection reagent R to estimate parameters for ligand binding and the stem strength ($K_L$, and the ratio $K_{H,D}/K_{H,D_L}$).  

To characterize the functionality of combinations of predicted aptamers and stems in switchable Aptabodies, our model describes binding of hemin $H$ and ligands $L$ to DNA-Aptabodies $D$, resulting in $D_L$, $D_H$ and $D_{LH}$. $D_H$ and $D_{LH}$ possess peroxidase activity and catalyze the luminol reaction (Figure 1). Table 1 shows the model equations. Therein, $k_L$ and $k_{-L}$ describe the binding and unbinding of the ligand $L$, $k_{H,D}$ and $k_{-H,D}$ binding and unbinding of hemin to the unligated AptaBody $D$, and $k_{H,D_L}$ and $k_{-H,D_L}$ of hemin to the ligand bound AptaBodies. Because a stronger enzymatic activity could be observed in the presence of the ligand, $k_{H,D_L}$ can be assumed to be larger than $k_{H,D}$.

Because none of the interaction species is in excess, we have to include equations also for $L$ and $H$ and cannot assume constant concentrations. In experiments, we left a time interval of several minutes between the mixture of $H$, $D$ and $L$, and the addition of the luminol reagent $R$ to obtain a steady state before starting the luminol reaction. For parameter estimations, because we were only interested in the binding constants $K_L= k_{-L}/k_{L}$, $K_{H,D}= k_{-H,D}/k_{H,D}$ and $K_{H,D_L}= k_{-H,D_L}/k_{H,D_L}$, we fixed the unbinding parameters $k_{-L}$, $k_{-L}$ and $k_{-L}$ to one, together with preponing the integration start time for the ODE solver relative to the time of luminol addition. This procedure forces the model to a steady state before the addition of luminol.  Then, sums of model variable values for $D_H$ and $D_{LH}$ can be fitted to values of experimentally determined enzyme activities. Therein, the parameter $k_{cat}$ is scaling factor between variables and measurements, which is estimated at the same time.

We estimated parameters for three experimentally tested kanamycin aptamers included in AptaBodies, one of them with two different stems, and a literature Aptamer variant. Figure 2A shows that the model can well explain the experimental data. When fitting $k_{H,D}$ and $k_{H,D_L}$ at the same time, we observed that only $k_L$ values were identifiable. Therefore, we decided to only estimate the ratios $K_{H,D}/K_{H,D_L}$. We were particularly interested in these ratios because they reflect the affinity change for hemin binding that is caused by ligand binding. When fitting the ratios together with $k_L$, all parameters were identifiable, which was assessed by profile likelihood estimation (Table 2). In Figure 2B, $K_L=1/k_L$ and the $K_{H,D}/K_{H,D_L}$ ratios are visualized for all tested candidates.

Figure 2. (A) Extracted enzyme activities together with model fits for predicted aptamer-stem combinations and a literature aptamer for kanamycin. (B) Estimated values of $K_L$ and of the ratios $K_{H,D}/K_{H,D_L}$ that reflect the switching dynamics of the stems (error bars: 95% confidence intervals from profile likelihood estimates).  

Table 2. Parameter estimates for switchable AptaBody candidates