\documentclass[a4paper,12pt,pdftex]{exam} \newcommand{\ptitle}{Activation curve} \input{../header.tex} \firstpagefooter{Supervisor: Lukas Sonnenberg}{}% {email: lukas.sonnenberg@student.uni-tuebingen.de} \begin{document} \input{../instructions.tex} Mutations in genes encoding ion channels can result in a variety of neurological diseases like epilepsy, autism, or intellectual disability. One way to find a possible treatment is to compare the voltage dependent kinetics of the mutated channel with its corresponding wild-type (non-mutated channel). Voltage-clamp experiments are used to measure and describe the kinetics. In the project you will compute and compare the activation curves of sodium channel, in particular the Nav1.6 wild-type (WT) channel and the A1622D mutation (the amino acid Alanine (A) at the 1622nd position is replaced by Aspartic acid (D)) that causes intellectual disability in humans. \begin{questions} \question In the accompanying datasets you find recordings of both wildtype and A1622D transfected cells. The cells were all clamped to a holding potential of $-70$\,mV for some time to bring all ion channels in the same closed states. Then the channels were activated by a step change in the command voltage to a value described in the \code{steps} vector. The corresponding recorded current \code{I} (in pA) and time \code{t} (in ms) traces are also saved in the files. \begin{parts} \part Plot all the current traces of a single WT and a single A1622D cell in two plots. Because the number of transfected channels can vary the peak values have little value. Normalize the curves accordingly (what kind of normalization would be appropriate?). Can you already spot differences between the cells? \part \textbf{I-V curve}: Find the peak values (minimum or maximum) for each voltage step and plot them against the steps. \part \textbf{Reversal potential}: Use the $I$-$V$-curve to estimate the reversal potential $E_\text{Na}$ of the sodium current. Consider a linear interpolation to increase the accuracy of your estimation. \part \textbf{Activation curve}: The activation curve is a representation of the voltage dependence of the sodium conductivity. It is computed with a variation of Ohm's law: \begin{equation} g_\text{Na}(V) = \frac{I_{peak}}{V - E_\text{Na}} \end{equation} \part \textbf{Comparison of the two ion channel types}: To compare WT and A1622D activation curves you should first parameterize your data. Fit a sigmoidal function \begin{equation} g_{Na}(V) = \frac{\bar g_\text{Na}}{1 + e^{ - \frac{V-V_{1/2}}{k}}} \end{equation} to the activation curves. With $\bar g_\text{Na}$ being the maximum conductivity, $V_{1/2}$ the half activation voltage and $k$ a slope factor (how these parameters influence the curve?). Now you can compare the two variants with three simple parameters. What do the differences mean? Which differences are statistically significant? \part \textbf{BONUS question}: Take a closer look at your raw data. What other differences can you see between the two types of sodium currents? How could you analyze these? \end{parts} \end{questions} \end{document}