Many potassium channels show voltage-dependent gating without a dedicated voltage sensor domain. This is not fully understood yet, but often explained by voltage-induced changes of ion occupation in the five distinct K+ binding sites in the selectivity filter. To better understand this mechanism of filter gating we measured the single-channel current and the rate constant of sub-millisecond channel closure of the viral K+ channel KcvNTS for a wide range of voltages and symmetric and asymmetric K+ concentrations in planar lipid membranes. A model-based analysis employed a global fit of all experimental data, i.e., using a common set of parameters for current and channel closure under all conditions. Three different established models of ion permeation and various relationships between ion occupation and gating were tested. Only one of the models described the data adequately. It revealed that the most extracellular binding site (S0) in the selectivity filter functions as the voltage sensor for the rate constant of channel closure. The ion occupation outside of S0 modulates its dependence on K+ concentration. The analysis uncovers an important role of changes in protein flexibility in mediating the effect from the sensor to the gate.
Transport through ion channels can be controlled by membrane potential, e.g. during the excitation of neurons and muscle cells1,2. In Kv channels, voltage sensitivity is conferred by the voltage-sensing domain (VSD), which is coupled to the conserved K+ channel pore domain. The VSD consists of a tetramer of four transmembrane helices per subunit, one carrying 4–5 positive charges3. Its function is quite well understood4,5.
However, also channels without a VSD can exhibit voltage sensitivity. This is for example important in K2P channels, which modulate in this way their slow inactivation6. In addition to these slow events, which occur in a time window of several tens of ms, also voltage-sensitive gating events in the millisecond7,8,9,10 and microsecond range11,12,13,14 have been described. These fast events can cause a negative slope in the apparent single-channel current-voltage relationship (IV curve)11,12,14. The mechanism of voltage dependence without VSD is still vague. C-type inactivation seems to be related to the ion occupation in the selectivity filter6,15,16,17, and also in Ca2+-gated MthK channels, the voltage-dependent gate has been located in the filter18. It has been proposed that the positive charges of the transported ions compensate the repulsive forces of the negative charges of the carbonyl groups lining the selectivity filter. Voltage-induced ion depletion of the binding sites consequently modifies the conformation of the filter19,20,21,22 and thus modulates the rate constants of gating. So far, evidence for the relationship between ion occupancy and conformation has been provided by crystallographic23,24, electron cryomicroscopy (cryo EM)25 or nuclear magnetic resonance (NMR) studies26,27,28 and computational modeling6,29,30,31,32.
To test the predictions from these approaches it is desirable to determine the postulated changes in ion distribution directly from the same single-channel recordings, which are also used for the quantitative description of the voltage-dependent gating. For several reasons, the viral K+ channels of the Kcv family are very appropriate candidates for such a study. First, they have a high unitary conductance, which supports high-resolution single-channel analysis33,34. Second, they exhibit a distinct voltage sensitivity, resulting in a very pronounced negative slope of the apparent single-channel IV curve14,33,34. It has been shown that the related reduction of the apparent current results from averaging over a normally hidden gating process with dwell times in the closed state between 50 and 150 µs (sub-millisecond gating). The overall voltage dependence of this gating process corresponds to the transfer of one electrical charge through the whole electric field14. Third, the Kcv family has about 80 members with different functional characteristics caused by just a few different residues in the sequence35. This provides guidelines for efficient mutational studies34. Fourth, a channel monomer consists of only 80 to 120 residues35. The combination of small size, high unitary conductance and distinct gates increases the possibility of assigning each distinct gate to a defined molecular mechanism.
Here, we employ a novel approach to determine ion distribution in the selectivity filter from single-channel recordings using a model-based IV curve analysis36. This is encouraged by previous studies, where simple Markov models for ion transport comprising loading, translocation and recycling steps have yielded important insights such as the binding order in cotransporters37 or the effect of internal pH on H+ pump stoichiometry38. In bacteriorhodopsin, several models of transport could be distinguished39. In the influenza A proton channel M2, we could verify the rapid exchange of protons between cytosol and the His37 proton binding site, the resetting of the tilted helix after each translocation cycle, transinhibition of ion uptake by cytosolic H+ concentration, and the origin of rectification40. In KcsA, a “mesoscopic” approach has been suggested combining Markov models and structural information41.
Now, atomistic models of ion transport through the selectivity filter in K+ channels have become available31,42,43. This opens the access to the evaluation of the voltage-dependent ion distribution in K+ channels from functional data. Here, we use single-channel data to test three different models for K+ transport through the selectivity filter of the viral channel KcvNTS. For this K+ channel, we have found that only the 5-state ion-hopping model of Roux42 is consistent with the data. It can fit the voltage and K+ dependence of the IV curves and of the rate constant of channel closure in a global fit. The results identify the voltage sensor of this gating process and indicate that a change in protein flexibility rather than in conformation provides the link between sensor and gate.
The gating processes in KcvNTS
KcvNTS shows several distinct gating processes; in the recordings in Fig. 1a,b, long closed events (“S”) as well as shorter events (“M”) are visible. The faster process, causing the large open channel noise at negative voltages is voltage-dependent and partially suppressed at higher K+ concentrations (compare the traces at −120 mV for 100 and 1500 mM) as indicated by the increased asymmetry of the noise.
In a previous paper14, it has been found that the Markov model in Fig. 1d is adequate for describing the dominant gating processes of this channel. Two slow gating processes (labelled by S) can be clearly revealed by dwell time analysis34, as they reach the full closed level. Since these slow gating events contribute equally to the amplitude histograms in Fig. 1c (the basis for the gating analysis below), they all are merged into the O-S transitions in Fig. 1d, with O being the open state. Unlike the slow gating, the faster processes are not resolved by full transitions to the closed state. The O-M gating with dwell times in the closed state M between 50 and 150 µs only causes small peaks in Fig. 1a (labelled by “M”). The recordings obtained at different membrane voltages show that O-M gating is strongly voltage-dependent. This is remarkable since Kcv channels do not have a VSD. The time series obtained at different K+ concentrations (Fig. 1a,b) reveal that O-M gating is also strongly sensitive to the K+ concentration in the solutions. The third gating process (O-F) is even faster with dwell times in the closed state F between approximately 1 to 10 µs. Its existence becomes obvious only from the broadening of the noise of the apparent open state (label “F” in Fig. 1a).
The analysis of gating by extended beta distributions
Since O-M and O-F gating cannot be evaluated directly by dwell-time analysis or similar methods, we utilize extended beta distributions44. Fast gating events with rate constants even much higher than the cut-off frequency of the low-pass filter of the recording system cause increased open channel noise (Fig. 1a,b) and thus characteristic distortions of the current amplitude histograms (Fig. 1c). Thus, the fast rate constants can be determined by a fit algorithm adjusting them until the “theoretical” amplitude histogram matches the measured one.
In order to accurately reproduce the effects of the 4th-order Bessel filter used during the experiments and to allow for multi-state Markov models, we create the theoretical amplitude histogram by simulations. For each gating event, two random numbers are generated based on starting values of the rate constants in the model in Fig. 1d, one determining the sink state for a jump from the current source state, and one determining the dwell time in the source state before the jump occurs. After filtering the simulated time series of current, the histogram is calculated, and the base line noise is incorporated by a convolution of the amplitude histograms.
In repetitive runs, the rate constants of the model are varied by a Simplex algorithm45 until the amplitude histogram of the simulated time series shows a minimum deviation from that of the measured one. Details of this analysis in KcvNTS have been published previously14.
Figure 2a,b shows the voltage dependence of the rate constants of the model in Fig. 1d in symmetrical solutions of 500 mM KCl. The rate constant of channel closure, kOM, related to the O-M transitions is the most voltage-dependent one. The rate constant of opening, kMO, is less voltage-dependent. The O-F gating is scarcely voltage-dependent. The error bars are large because the O-F rate constants are at the edge of the temporal resolution. The weak voltage dependence of kOS and kSO at negative potentials is not significant, because the large error bars indicate the uncertainty of their determination. The O-S gating is not investigated here.
The analysis by extended beta distributions discriminates three different currents (Fig. 2c). The apparent current, Iapp, is obtained directly from the time series after averaging over 10 adjacent sampling points. The true open-channel current Itrue is the current, which would be measured with a fictional amplifier of infinite bandwidth and no noise. It can be revealed by fitting extended beta distributions to amplitude histograms. IOF is the current for the case that O-M gating would be fully resolved, and the amplifier averages only over O-F gating (Supplementary Eq. S1). Calculating Iapp by averaging over both the O-M and O-F gating results in the same value of Iapp as obtained directly from the time series (Supplementary Eq. S2). We have verified the reliability of the determination of IOF and Iapp previously14. For the sake of comparison, the experimental data generated for the investigation here was supplemented by a few data from this method paper14. Details are given in the respective Figure legends.
The O-M gating occurs in the selectivity filter
We have shown previously14 that in KcvNH, a close homologue of KcvNTS, the O-M gating is located in the selectivity filter. In Fig. 3, we show that this also holds for KcvNTS. The structural model of KcvNTS suggests that the mutation S42T affects the anchoring of the selectivity filter (Fig. 3a,b). In KcsA, mutations of the corresponding residue (E71) have dramatic effects on the hydrogen-bond network surrounding the selectivity filter and on C-type inactivation46. In KcvNTS the mutation strongly influences the gating at negative voltages (compare Fig. 3c, right panel, with Fig. 1a) and thus the slope of the amplitude histogram between the closed peak and the open peak at negative voltages (Fig. 3d,e). This region is shaped by the O-M gating14. Analysis by extended beta distributions reveals that the S42T mutation drastically reduces the rate constant kOM (Fig. 3f) and to a lesser extent kMO (Fig. 3g).
In contrast, mutations at G77 (Fig. 3a,b) influence a newly detected inner gate34. At negative potentials, G77S and G77T do not have a significant effect on the time series (Fig. 3c) and on kOM (Fig. 3f), where the curves merge into the slope, and on kMO (Fig. 3g). In contrast, they have a significant effect on kOM at positive voltages (Fig. 3c,f). The different action of the mutations at positive and negative voltages indicates that two different processes are involved in the O-M gating14. That one dominating at negative potentials is associated with the selectivity filter and that one at positive potentials with the inner gate14.
The dependence of O-M gating and current on K+ concentration and voltage
The assignment of the O-M gating to the selectivity filter (Fig. 3) raises the question of whether its voltage dependence originates from changes in the interaction between the permeant ions and the filter. The effect of ion occupation in the selectivity filter has been considered by several authors, e.g.6,10,47,48, based on the effect of permeant ions on gating.
Here, we employ a new approach to determine ion occupation in the filter from single-channel data. To this end, we determine the voltage dependence of the rate constants kOM and kMO of the O-M gating and of the open-channel current over a wide range of symmetrical and asymmetrical K+ concentrations, from 50 or 100 mM to 1500 mM (Fig. 4).
The IV curves (Fig. 4a–c) are about linear at symmetrical concentrations around 100 mM. This indicates that the voltage-sensitive ion translocation in the selectivity filter is not rate-limiting for the flux49. With increasing external K+ concentration, there is a weak exponential increase at negative voltages indicating that at high concentrations the voltage-sensitive translocation step starts to become rate limiting (Fig. 4c). This effect is much less pronounced at positive voltages for increasing internal concentrations (Fig. 4b) suggesting an asymmetry in the system. In symmetrical solutions (Fig. 4a), the effect of external concentrations dominates at negative voltages and the effect of internal concentrations at positive voltages (Fig. 4b).
The rate constant of channel closure, kOM, increases exponentially at negative voltages. It is strongly left-shifted with increasing internal K+ concentrations (Fig. 4e). Plotting kOM versus the K+ motive force Kmf = V − EK, with V being the membrane voltage and EK the reversal potential for K+, shows that kOM depends on the Kmf under these conditions (Fig. 4e, inset). Below, this feature is discussed as a stronghold of our analysis as it is quite unexpected in terms of the relation between ion concentration at site S0 and the sensitivity of kOM to internal K+ concentrations. In contrast, external K+ concentration has no effect (Fig. 4f) on kOM at negative voltages. At positive voltages, kOM is nearly voltage-independent, and the effect of K+ concentration is quite different from that at negative voltages as increasing internal K+ has no effect (Fig. 4e), whereas increasing external K+ has a strong effect (Fig. 4f).
The rate constant of channel opening, kMO, is also quite constant at positive voltages (Fig. 4g,h,i). The exponential dependence on negative voltages is opposite and less steep than that of kOM. The magnitude of the effect of K+ concentrations is similar for internal and external concentrations, but the effect is of opposite sign (Fig. 4h,i).
Model-based IV curve analysis
Models of ion permeation
Figure 3 shows that the O-M gating is physically located in the selectivity filter. Its sensitivity to voltage and K+ suggests that it reflects a distinct occupation of the filter by K+ ions. In Fig. 5a to c, three different models42,43 for ion hopping in the selectivity filter50 during the open state are used for setting up the equations for a quantitative analysis.
The equations for the fit of the IV curves
We start the analysis with the model in Fig. 5a42 in order to investigate whether there is a set of rate constants of ion hopping, which can create the occupation probabilities Pm of the 5 states in the model. They determine the voltage dependence of measured current (IV curves) as well as that of the rate constant of channel closing kOM for all K+ concentrations shown in Fig. 4. Here, only the central equations are listed. A full description is provided in Supplementary Eqs S3–S7.
The open channel current can be calculated from the rate constants kij between the states in Fig. 5a.
e is the unit charge, the numbers 1–5 represent the states in the ion-hopping model in Fig. 5a. The sum of the five 5 × 5 D-matrices in the denominator results in 100 products of 4 rate constants (Supplementary Eq. S4). As justified in Supplementary Note 1, IOF (Fig. 2c, Supplementary Eq. S1) is used as effective current in Eq. 1 as it accounts for the averaging over the O-F gating occurring prior to an open-closed transition of the O-M gating.
The binding reactions k12 and k54 are proportional to the ion activities aK (instead of concentrations, see Supplementary Table S1)
The last index “1” labels the rate constants for aK = 1 mM.
The two most voltage-dependent reactions are those where two ions move simultaneously through the centre of the selectivity filter. The effect of voltage on the other reactions is expected to be small, since 80% of the voltage is assumed to drop over the selectivity filter51,52,53. Assuming an Eyring barrier at the electrical position sij (i,j = 2,3 and 5,1) leads to
The equations for the fit of the k OM(V) curves
The modulation of the forces between ions and protein occurs on the time scale of permeation, i.e. around 10 ns. In contrast, gating is much slower. Thus, the effect of ion occupation on gating results from a long-term integration over those forces and is related to the steady-state ion occupation probabilities Pm (m = 1 to 5) of the model in Fig. 5a. They are calculated by means of the D-matrices, which occur in Eq. 1 and are described in Supplementary Eq. S4.
An enzyme is a protein where an allosteric site can influence the kinetics of the active site. In analogy to this, an ion channel can be seen as a protein, where an “allosteric site” can influence the kinetics of a distant gate. Considering what is known about the mechanism of the action of an allosteric site on enzyme activity, we have to consider two different mechanisms, which may mediate the allosteric effect of Pm on gating. As discussed in detail below, this can be achieved by a change in conformation or a change in flexibility19. Thus, we must distinguish between two basically different possible mechanisms.
The forces between ions and carbonyl groups cause a conformational change at the site of the gate. In this case, we expect that kOM is proportional to one or more of the occupation probabilities Pm of state m (m = 1 to 5) in the model of Fig. 5a.
The forces between ions and selectivity filter cause a change in the flexibility of the protein. As discussed in detail below, such an effect is well-known from the allostery of enzymes and is also considered for ion channels. In that case, kOM would be related to 1/Pm (details see Discussion and Eq. 8, below).
Thus, we start with a test of the following relationships
with w being a scaling factor independent of voltage and K+ concentration, and m = 1 to 5.
Identification of the voltage-sensing binding site(s) by a global fit of the IV curves and k OM(V)
We search for a set of rate constants of the ion hopping model in Fig. 5a, which can create the measured IV curves as well as the measured dependence of kOM (related to appropriate ion distributions Pi, Eqs 4,5) on negative voltage and K+ concentration.
This is achieved by a global fit of the IV curves in Fig. 4a to c and the kOM(V) curves in Fig. 4d to f including all 36 curves (18 for IV and 18 for kOM(V)) obtained with different K+ concentrations. For the IV curves, Eq. 1 is used. For kOM(V), one of the 10 equations given by Eq. 5a,b is employed (for m = 1 to 5). However, to give about equal weight in the fitting routine to the IV curves and the rate constant ln(kOM) is fitted. The global fit implies that for both equations (Eq. 1 and one of Eq. 5a,b) the identical set of free parameters is used. These are the rate constants kij of the ion hopping model in Fig. 5a, the parameters s51, s23, V51 and V23 of the Eyring barriers (Eq. 3) and the scaling factor w in Eq. 5.
The resulting error sums from the global fits provide a measure of how well each one of the 10 options (Eq. 5a,b) is in agreement with the data (Table 1). The lowest error sum and thus the best fit is achieved for the global fit of the IV curve together with kOM = w*1/P3 (Supplementary Fig. S1). Other ion occupancies than 1/P3 result in significantly worse fits (Table 1 and Supplementary Fig. S2). Interestingly, P3 is the only occupation pattern in the conduction cycle with three ions in the filter and in which the outermost binding site S0 is occupied (Fig. 5a). In other words, the probability of channel closing is increased when the number of ions in the filter decreases and S0 becomes empty. The involvement of S0 is not surprising because negative voltage pulls the ions away from S0.
The fit, which uses kOM = w*1/P3, matches the measured IV curves quite well and also the voltage dependence of kOM (Supplementary Fig. S1). However, the fit overestimates the concentration dependence of kOM on symmetrical KCl. The concentration dependence and even the steepness of the voltage dependence of the fit can considerably be improved (Table 1) by incorporation of P4, the neighbouring state of P3, by means of the equation
with w also here being a constant scaling factor. The parameters of the global fits of the IV curves and ln(kOM) = ln(w P4/P3) are provided in Supplementary Table S2. The IV curves are well fitted, and good fits of the concentration dependence of kOM are obtained (Fig. 6d–f) except for some minor deviations at extreme negative voltages where the characteristics of the amplitude histograms become less pronounced.
In the 5-state ion hopping model of Fig. 5a, the occupation patterns of states 3 and 4 are very similar. The only difference is that the ion, which occupies S0 in state 3 (P3), is in the outer pore mouth outside of S0 in state 4 (P4). States 3 and 4 do not occur simultaneously. However, at a current of 16 pA one transport cycle takes 10 ns. Thus, on the time scale of kOM, the protein feels the averaged effects of P3 and P4 simultaneously. The qualitative mechanistic interpretation of Eq. 6 is: Three ions in the filter including S0 (P3) stabilize the open state via an increase in rigidity (decrease in flexibility), and an ion in the outer pore mouth (P4) destabilizes the open state via a conformational change or a change in force (Eq. 8, below). Evidence for the reliability of the fitting routines is provided in Supplementary Note 2.
Test of alternative models of ion permeation
We tested, whether the model can fit the experimental data when the binding site for the outer ion (state 4 of Fig. 5a) is omitted. For fits based on the resulting 4-state model in Fig. 5b, again all assignments kOM(V) to Pm or 1/Pm (m = 1 to 4) were tested in global fits with the IV curves. Eqs 2 and 3 were also used here. Similar to the 5-state model in Fig. 5a used above, the voltage dependence could only be reproduced by assuming kOM = w*1/P3 (Supplementary Fig. S3). However, this model failed to provide the dependence on K+ concentration. In contrast to the model in Fig. 5a, this could not be repaired by providing a partner for 1/P3 as in the case of kOM = w P3/P4 in the 5-state model in Fig. 5a. This indicates the necessity of state 4 in Fig. 5a.
In the case of the “hard knock-on” model43, an appropriate assignment of Eqs 2 and 3 (Supplementary Eqs S15–S17) led to a 5-state model with a different topology as in Fig. 5a. This model (Fig. 5c) was unable to reproduce the voltage dependence of kOM. Again, all assignments of kOM to Pm or 1/Pm were tested. The “best” fit is shown in Supplementary Fig. S4.
The understanding of an a priori non-intuitive action of external K+ concentration
Unexpected is the finding in Fig. 4f that kOM at negative voltages is not sensitive to external K+ concentration. In the light of the above mechanism of ion depletion around S0 it would be assumed that increasing external K+ concentration would increase P3 and thus decrease kOM. Inspection of P4 in Fig. 7 provides an explanation for the conundrum. At −160 mV, the effects of K+ concentration on P3 (ion at S0) and P4 (ion outside of S0) are similar (Fig. 7i and l), thus compensating each other in the ratio P3/P4. This compensation levels off when the voltage approaches 0 mV (Fig. 6f), thus reproducing the experimental finding in Fig. 4f. In symmetrical solutions, there is a partial compensation (Figs 6d and 7g,j). The numerical details of these effects are given in Supplementary Eq. S14.
Changing internal K+ concentration results in a dependence of k OM on driving force but does not allow a straight-forward identification of the location of the sensor
In contrast to external K+ concentrations discussed above, internal K+ concentrations do not have similar effects on P4 and P3 (Fig. 7h,k). Thus, the K+ effect on 1/P3 (Fig. 7h) becomes dominant as it is not compensated (Fig. 4e). The effect of varying internal K+ concentration can be accounted for by the Kmf, the sum between (weighted) electrical potential, V and Nernst potential (EK) (inset of Fig. 4e). The numerical origin for the dependence on Kmf for internal concentrations is given in Supplementary Eqs S8–S13, resulting in an equation of the form
Kmf1 and Kmf2 account for the fact that different fractions of voltage are felt by the involved reactions.
This result demonstrates that an effect of internal concentration on kOM cannot automatically be taken as evidence for an internal localization of the sensor for kOM. The analysis reveals that high internal concentrations hinder the withdrawal of ions from S0, and that this is not compensated by P4.
The adequate permeation model for KcvNTS and identification of the ion occupation acting as a sensor for voltage-dependent O-M gating
The present study demonstrates the benefits of combining information from single-channel recordings and structural models for ion transport through the selectivity filter of a viral K+ channel.
From crystal structure analysis, it is known that the permeating ions occupy distinct binding sites in the selectivity filter23,51,54,55. This implies that transport occurs via hopping of the ions from one binding site to the next50. This process can be described by continuum or discrete approaches. For the continuum approaches, electro diffusion as described by the Poisson-Nernst-Planck equation is suggested56. Others57 argue that this approach has its limitations like the failure to distinguish between Na+ and K+ ions. They suggest to account for protein-ion interaction by incorporating changes in the dielectric constant via the Born equation. In the discrete approaches, the rate constants of ion hopping are determined from molecular dynamics (MD) simulations. Here, the problems are in the assumption of the correct simulation parameters leading to different permeation models as in Fig. 5a,c.
However, the individual problems of these approaches are not a concern, but an incentive for our investigation. We want to provide numerical parameters obtained from experiments, namely the ion occupation from the measured IV curves as provided by the fits described above. They can be used in subsequent approaches as a test of the predictions of the theoretical models by interactive mutual improvements of experimental approaches as provided here and computational approaches by Born-Poisson-Nernst-Planck or MD simulations.
For KcvNTS, the best fits in a comparative model-based analysis are obtained with the 5-state model of ion hopping42 (Fig. 5a). The two alternative models (Fig. 5b,c) were not able to provide an adequate fit of the experimental data in the same frame of simple relationships. Of course, it can be argued that a more complex function of a weighted distribution of more than two states could also lead to successful fits in the case of the other models. However, we apply Occam’s Razor, i.e., giving preference to that model, which gives the simplest relationship. A stronghold of the model is the correct prediction of the non-intuitive asymmetrical action of internal and external K+ concentration.
The voltage dependence of the rate constant kOM, which is responsible for the apparent negative slope conductance in this channel, can fully be explained by the reduction of the number of K+ ions in the selectivity filter by the depletion of the binding site S0. This depletion on the external side of the selectivity filter is the result of an increasing inward current IOF where negative voltage pulls the ions away from S0.
The mediator between sensor and gate: changes in conformation or flexibility?
A peculiarity in the fitting with the 5-state model42 and also the 4-state model is that the best results are obtained with a dependence of kOM on 1/P3. It may be considered that the effect of ion depletion at S0 could also be obtained by a more straight-forward term like 1-P3 in the global fits. However, in contrast to 1/P3, 1-P3 cannot account for the whole range of experimental values of kOM (Fig. 6), which change with negative voltage over two orders of magnitude. Thus, we have to think of a likely molecular mechanism, which is able to account for this unusual relationship.
A possible explanation comes from the comparison of enzymes and ion channels. Both types of proteins can have allosteric sites, where a modulator (ligand) binds, and a distant active (orthosteric) site. The mechanisms of coupling between these sites are well-understood in enzymes since they are easier to crystalize. Thus, they provide suggestions for the phenomena investigated here. The carbonyl groups of the selectivity filter can be seen as the “allosteric site” in which the complexed ion acts as an “allosteric modulator”23,24,29,31. The active site is a still unknown gate.
Following this analogy, an ion could modulate the performance of the protein via two different mechanisms: a change in conformation or a change in flexibility. A modulatory impact of flexibility on protein function is well known from allostery in enzymes and documented by far infrared (FIR) spectroscopy58, change in melting temperature59, neutron scattering60, crystal structure B-factors61 or from computational studies62. The change in flexibility seems to play a more important role than usually anticipated. The modulation of an active site by an allosteric site in these systems is not only mediated by long-range conformational changes, but also by changes in the flexibility without obvious conformational changes63. Panjkovich and Daura64 performed normal-mode analysis and observed significant changes in protein flexibility upon allosteric ligand binding in 70% of the investigated cases.
This general phenomenon of protein flexibility seems to be relevant also in ion channels. For example, the snug fit model for selectivity55 has been replaced by models considering the flexibility of the selectivity filter65. Further examples for a role of protein flexibility in relation to structure and function of ion channels are also known for gramicidine A19,21,66, K+ channels19,20,67,68, NavAb22 or a CNG chimera69. Also in the model K+ channel KcsA, infrared (IR) spectroscopy has demonstrated that exchanging Na+ for K+ in the filter changes the vibrational modes of the ion-coordinating carbonyls70.
In the context of the present analysis we can speculate that a change in flexibility (or stiffness K) can cause a kink or an angle of a turn Δx at the O-M gate according to the law of a spring19.
Thus, if the ion at site S0 increases stiffness, P3 is in the denominator. P4 is a possible candidate for modulating the force F.
P4 could also act via a change in flexibility since ligand binding can do both, increase or decrease flexibility. Such a behaviour was found in the activation in rhodopsin-like G protein-coupled receptors. It can constrain the movement of the retinal β–ionone ring (corresponding to P4) while at the same time increasing the flexibility in the ligand chain (corresponding to 1/P3)71.
In KcsA, the mutation E71A (corresponding to S42T in KcvNTS, Fig. 3a,b) causes a profound rearrangement of the hydrogen-bond network surrounding the selectivity filter46. For the study of the detailed mechanism of the hypothetical connection between the sensor S0 and the still unknown O-M gate in KcvNTS, this finding may serve as a first incitement to check whether such an effect is also involved in KcvNTS.
The model-based IV curve analysis has identified the pattern of ion occupation in the selectivity filter responsible for O-M channel closure at negative voltages in the viral K+ channel KcvNTS. The confidence in this approach is supported by a correct and detailed description of the voltage- and K+-dependent sub-ms gating in the selectivity filter. The same analysis performed for other channels and other kinds of gating like C-type inactivation will provide an answer to the question of whether this mechanism holds also for other channels and which types of gating are correlated with which patterns of ion distribution in the selectivity filter. The present analysis does not answer the question of the nature of the gate. However, a combination of model-based IV curve analysis with measurements of protein flexibility supported by mutational studies, which address the putative link between the sensor and the gate, are expected to solve this problem. Furthermore, the rate constants reach a range, which in near future may by accessible to determination of the rate constants by computational methods.
In vitro protein expression and purification
KcvNTS is a member of the ATCV subfamily of the Kcv family33,72. The virus encoding for the channel was originally isolated from an alkaline lake in Nebraska73. The proteins were expressed in vitro and purified as described previously34. Briefly, the gene of KcvNTS was cloned into a pEXP5-CT/TOPO®-vector (Invitrogen, Karlsbad, CA, USA), the fusion of the His tag coded for in the plasmid was prevented by inserting a stop codon. Mutations were introduced by site-directed mutagenesis, following the QuickChange method74. All mutants were sequenced.
In vitro expression of the channel protein was performed with the MembraneMaxTM HN Protein Expression Kit (Invitrogen) following the manufacturer’s instructions. During the expression procedure, the KcvNTS proteins were directly embedded into nanolipoproteins (NLPs)75. The NLPs contained multiple His-tags, allowing the purification of the native KcvNTS proteins by metal chelate affinity chromatography. Purification was done on a 0.2 mL HisPurTM Ni-NTA spin column (ThermoFisher Scientific, Waltham, MA, USA). Divergent from the manufacturer’s instructions, the column was washed three times with two resin-bed volumes of 20 mM imidazole to remove unspecific binders. The KcvNTS-containing NLPs were then eluted in three fractions (200 µL each) with 250 mM imidazole. Neither the washing nor the elution solutions contained salts; this improves the reconstitution efficiency into the bilayer76.
Lipid bilayer experiments
Planar lipid bilayer experiments were performed at room temperature (20–25 °C) with a vertical bilayer setup (IonoVation, Osnabrück, Germany). The recording chambers were prepared as described previously72, and 1,2-diphytanoyl-sn-glycero-3-phosphocholine (DPhPC, Avanti Polar Lipids, Alabaster, AL, USA) bilayers were formed using the pseudo painting/air bubble technique77. For reconstitution of the channel protein, one of the elution fractions was diluted in 250 mM imidazole solution by a factor of 1000 to 100,000, and a small amount (1–3 µL) of the diluted NLP/KcvNTS-conjugates was added directly below the bilayer in the trans compartment with a bent Hamilton syringe.
After verifying the incorporation of a single channel in the lipid bilayer by short voltage pulses, constant voltages between +160 mV and −160 mV in steps of 20 mV were applied for 1 to 5 minutes. Both compartments of the bilayer chamber were connected with Ag/AgCl electrodes to the headstage of a patch-clamp amplifier (L/M-EPC-7, List-Medical, Darmstadt, Germany). Membrane potentials were applied to the cis compartment, the trans compartment was grounded. Experiments with asymmetrical KCl concentrations were performed with 3 M KCl agar bridges. K+ concentration was changed by replacing an appropriate amount of the solution in the recording chamber by a 500 mM, 1.5 M or 3 M KCl stock solution and thorough mixing. All solutions and stock solutions contained 10 mM HEPES, pH was adjusted to 7.0 with KOH. The asymmetric nature of the apparent IV curves (Fig. 2c) of Kcv channels33 allows the identification of the orientation of the channel in the bilayer. In all graphs, positive currents corresponded to outward currents in the in vivo situation. Currents were filtered with a 1-kHz 4-pole Bessel filter and digitized with a sampling frequency of 5 kHz (LIH 1600, HEKA Elektronik, Lambrecht, Germany).
Correction of electrode potentials
During the long experiments (up to 10 hours for the recording of steady-state IV curves in up to 10 different KCl concentrations), the electrode potential could drift by about 2 to 20 mV (the average of absolute values was 4 mV) despite the use of agar bridges. Since K+ is the only cation present in the solution, the reversal potential could be corrected retroactively. To this end, the measured apparent reversal potential of the IV curve of IOF (definition in Supplementary Eq. S1) was determined by a 3rd-order polynomial fit. The rate constants and currents for each individual voltage protocol were then shifted along the V-axis accordingly. In cases where several experiments were averaged, the data points were interpolated with a cubic spline function before averaging. Changes in the KCl concentrations did not occur because of the large volume of the chambers (2.5 mL).
Determination of I true and the rate constants of fast gating from extended beta distribution analysis
Gating is strongly attenuated if its rate constants are higher than the low-pass filter frequency of the set-up. Under these circumstances, neither the individual gating transitions, nor the true open channel current, Itrue, can be directly observed. Fortunately, gating causes “excess noise”44,78, which causes broadened, non-Gaussian peaks in the amplitude histograms (see Figs 1c and 3d,e). From the deviations of the measured amplitude histograms from that one resulting from the Gaussian baseline noise, the hidden gating processes can be resolved by extended beta distribution analysis44 using our lab-made program “bownhill”. The analysis is based on the simulation of theoretical time series from a Markov model of gating (Fig. 1d), and thus it can include without any simplifying assumptions all peculiarities of the individual experiments, like set-up noise, characteristics of the higher order low-pass filter, and adequate multi-state Markov model of gating44. Details of the application of this analysis to gating in KcvNTS have been described previously14. The program bownhill can be downloaded from http://www.bio.tu-darmstadt.de/ag/professuren/indraschroeder/software.en.jsp.
The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.
Hodgkin, A. L. & Huxley, A. F. A quantitative description of membrane current and its application to conductance and excitation in nerve. J. Physiol. 117, 500–544 (1952).
Hille, B. Ion channels of excitable membranes. (Sinauer Associates, Inc., 2001).
Zhao, J. & Blunck, R. The isolated voltage sensing domain of the Shaker potassium channel forms a voltage-gated cation channel. Elife 5, (2016).
Bezanilla, F. Voltage-gated ion channels. IEEE Trans. Nanobioscience 4, 34–48 (2005).
Börjesson, S. I. & Elinder, F. Structure, function, and modification of the voltage sensor in voltage-gated ion channels. Cell Biochem. Biophys. 52, 149–174 (2008).
Schewe, M. et al. A non-canonical voltage-sensing mechanism controls gating in K2P K+ channels. Cell 164, 937–949 (2016).
Lu, T., Wu, L., Xiao, J. & Yang, J. Permeant ion-dependent changes in gating of Kir2.1 inward rectifier potassium channels. J. Gen. Physiol. 118, 509–522 (2001).
Choe, H., Sackin, H. & Palmer, L. G. Gating properties of inward-rectifier potassium channels: Effects of permeant ions. J. Membr. Biol. 184, 81–89 (2001).
Thomson, A. S. & Rothberg, B. S. Voltage-dependent inactivation gating at the selectivity filter of the MthK K+ channel. J. Gen. Physiol. 136, 569–579 (2010).
Piskorowski, R. A. & Aldrich, R. W. Relationship between pore occupancy and gating in BK potassium channels. J. Gen. Physiol. 127, 557–576 (2006).
Schroeder, I. & Hansen, U.-P. Saturation and microsecond gating of current indicate depletion-induced instability of the MaxiK selectivity filter. J. Gen. Physiol. 130, 83–97 (2007).
Schroeder, I., Thiel, G. & Hansen, U.-P. Ca2+ block and flickering both contribute to the negative slope of the IV curve in BK channels. J. Gen. Physiol. 141, 499–505 (2013).
Abenavoli, A. et al. Fast and slow gating are inherent properties of the pore module of the K+ channel Kcv. J. Gen. Physiol. 134, 219–229 (2009).
Rauh, O. et al. Extended beta distributions open the access to fast gating in bilayer experiments-assigning the voltage-dependent gating to the selectivity filter. FEBS Lett. 591, 3850–3860 (2017).
Kiss, L. & Korn, S. J. Modulation of C-type inactivation by K+ at the potassium channel selectivity filter. Biophys. J. 74, 1840–1849 (1998).
Hoshi, T. & Armstrong, C. M. C-type inactivation of voltage-gated K+ channels: Pore constriction or dilation? J. Gen. Physiol. 141, 151–160 (2013).
Ogielska, E. M. & Aldrich, R. W. Functional consequences of a decreased potassium affinity in a potassium channel pore: ion interactions and C-type inactivation. J. Gen. Physiol. 113, 347–358 (1999).
Posson, D. J., McCoy, J. G. & Nimigean, C. M. The voltage-dependent gate in MthK potassium channels is located at the selectivity filter. Nat. Struct. Mol. Biol. 20, 159–66 (2013).
Allen, T. W., Andersen, O. S. & Roux, B. On the importance of atomic fluctuations, protein flexibility, and solvent in ion permeation. J. Gen. Physiol. 124, 679–690 (2004).
Grottesi, A., Domene, C., Haider, S. & Sansom, M. S. P. Molecular dynamics simulation approaches to K channels: Conformational flexibility and physiological function. IEEE Trans. Nanobioscience 4, 112–120 (2005).
Baştuğ, T., Gray-Weale, A., Patra, S. M. & Kuyucak, S. Role of protein flexibility in ion permeation: A case study in gramicidin A. Biophys. J. 90, 2285–2296 (2006).
Boiteux, C., Vorobyov, I. & Allen, T. W. Ion conduction and conformational flexibility of a bacterial voltage-gated sodium channel. Proc. Natl. Acad. Sci. 111, 3454–3459 (2014).
Zhou, Y., Morais-Cabral, J. H., Kaufman, A. & MacKinnon, R. Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolution. Nature 414, 43–48 (2001).
Cuello, L. G. et al. Structural basis for the coupling between activation and inactivation gates in K+ channels. Nature 466, 272–275 (2010).
Hite, R. K. et al. Cryo-electron microscopy structure of the Slo2.2 Na+-activated K+ channel. Nature 527, 198–203 (2015).
Baker, K. A., Tzitzilonis, C., Kwiatkowski, W., Choe, S. & Riek, R. Conformational dynamics of the KscA potassium channel governs gating properties. Nat Struct Mol Biol 14, 1089–1095 (2007).
Ader, C. et al. A structural link between inactivation and block of a K+ channel. Nat. Struct. Mol. Biol. 15, 605–612 (2008).
Imai, S., Osawa, M., Takeuchi, K. & Shimada, I. Structural basis underlying the dual gate properties of KcsA. Proc. Natl. Acad. Sci. USA 107, 6216–6221 (2010).
Miloshevsky, G. V. & Jordan, P. C. Conformational changes in the selectivity filter of the open-state KcsA channel: an energy minimization study. Biophys. J. 95, 3239–3251 (2008).
Capener, C. E., Proks, P., Ashcroft, F. M. & Sansom, M. S. P. Filter flexibility in a mammalian K channel: models and simulations of Kir6.2 mutants. Biophys. J. 84, 2345–2356 (2003).
Bernèche, S. & Roux, B. A gate in the selectivity filter of potassium channels. Structure 13, 591–600 (2005).
Domene, C., Klein, M. L., Branduardi, D., Gervasio, F. L. & Parrinello, M. Conformational changes and gating at the selectivity filter of potassium channels. J. Am. Chem. Soc. 130, 9474–9480 (2008).
Gazzarrini, S. et al. Chlorella virus ATCV-1 encodes a functional potassium channel of 82 amino acids. Biochem. J. 420, 295–303 (2009).
Rauh, O. et al. Identification of intrahelical bifurcated H-bonds as a new type of gate in K+ channels. J. Am. Chem. Soc. 139, 7494–7503 (2017).
Thiel, G. et al. Minimal art: Or why small viral K+ channels are good tools for understanding basic structure and function relations. Biochim. Biophys. Acta 1808, 580–588 (2011).
Hansen, U.-P., Rauh, O. & Schroeder, I. A simple recipe for setting up the flux equations of cyclic and linear reaction schemes of ion transport with a high number of states: the arrow scheme. Channels 10, 1–20 (2016).
Sanders, D. & Hansen, U.-P. Mechanism of Cl- transport at the plasma membrane of Chara corallina: II. transinhibition and the determination of H+/Cl− binding order from a reaction kinetic model. J. Membr. Biol. 58, 139–153 (1981).
Sanders, D., Hansen, U.-P. & Slayman, C. L. Role of the plasma membrane proton pump in pH regulation in non-animal cells. Proc Natl Acad Sci USA 78, 5903–5907 (1981).
Gradmann, D., Berndt, A., Schneider, F. & Hegemann, P. Rectification of the channelrhodopsin early conductance. Biophys. J. 101, 1057–1068 (2011).
DiFrancesco, M. L., Hansen, U.-P., Thiel, G., Moroni, A. & Schroeder, I. Effect of cytosolic pH on inward currents reveals structural characteristics of the proton transport cycle in the influenza A protein M2 in cell-free membrane patches of Xenopus oocytes. PLoS One 9, e107406 (2014).
Oiki, S., Iwamoto, M. & Sumikama, T. Cycle flux algebra for ion and water flux through the KcsA channel single-file pore links microscopic trajectories and macroscopic observables. PLoS One 6, (2011).
Roux, B. Ion conduction and selectivity in K+ channels. Annu. Rev. Biophys. Biomol. Struct. 34, 153–171 (2005).
Köpfer, D. A. et al. Ion permeation in K+ channels occurs by direct Coulomb knock-on. Science 346, 352–355 (2014).
Schroeder, I. How to resolve microsecond current fluctuations in single ion channels: The power of beta distributions. Channels 9, 262–280 (2015).
Caceci, M. S. & Cacheris, W. P. Fitting curves to data - The simplex algorithm is the answer. BYTE 5, 340–362 (1984).
Cordero-Morales, J. F., Jogini, V., Chakrapani, S. & Perozo, E. A multipoint hydrogen-bond network underlying KcsA C-type inactivation. Biophys. J. 100, 2387–2393 (2011).
Demo, S. D. & Yellen, G. Ion effects on gating of the Ca2+-activated K+ channel correlate with occupancy of the pore. Biophys. J. 61, 639–48 (1992).
López-Barneo, J., Hoshi, T., Heinemann, S. H. & Aldrich, R. W. Effects of external cations and mutations in the pore region on C-type inactivation of Shaker potassium channels. Recept. Channels 1, 61–71 (1993).
Hansen, U.-P., Gradmann, D., Sanders, D. & Slayman, C. L. Interpretation of current-voltage relationships for ‘active’ ion transport systems: I. Steady-state reaction-kinetic analysis of class-I mechanisms. J. Membr. Biol. 63, 165–190 (1981).
Miller, C. Ionic hopping defended. J. Gen. Physiol. 113, 783–787 (1999).
Jiang, Y. et al. The open pore conformation of potassium channels. Nature 417, 523–546 (2002).
Contreras, J. E. et al. Voltage profile along the permeation pathway of an open channel. Biophys. J. 99, 2863–2869 (2010).
Andersson, A. E. V., Kasimova, M. A. & Delemotte, L. Exploring the viral channel KcvPBCV-1 function via computation. J. Membr. Biol. in press (2018).
Kuo, A. et al. Crystal structure of the potassium channel KirBac1.1 in the closed state. Science. 300, 1922–1926 (2003).
Doyle, D. A. et al. The structure of the potassium channel: Molecular basis of K+ conduction and selectivity. Science. 280, 69–77 (1998).
Liu, J.-L. & Eisenberg, B. Poisson-Nernst-Planck-Fermi theory for modeling biological ion channels. J. Chem. Phys. 141, 22D532, https://doi.org/10.1063/1.4902973 (2014).
Liu, X. & Lu, B. Incorporating Born solvation energy into the three-dimensional Poisson-Nernst-Planck model to study ion selectivity in KcsA K+ channels. Phys. Rev. E 96, 62416 (2017).
Whitmire, S. E. et al. Protein flexibility and conformational state: A comparison of collective vibrational modes of wild-type and D96N bacteriorhodopsin. Biophys. J. 85, 1269–1277 (2003).
Cimmperman, P. et al. A quantitative model of thermal stabilization and destabilization of proteins by ligands. Biophys. J. 95, 3222–3231 (2008).
Zaccai, G. How soft is a protein? A protein dynamics force constant measured by neutron scattering. Science. 288, 1604–1607 (2000).
Rafferty, J., Somers, W., Saint-Girons, I. & Phillips, S. Three-dimensional crystal structures of Escherichia coli met repressor with and without corepressor. Nature 341, 705–710 (1989).
Dobbins, S. E., Lesk, V. I. & Sternberg, M. J. E. Insights into protein flexibility: The relationship between normal modes and conformational change upon protein-protein docking. Proc. Natl. Acad. Sci. 105, 10390–10395 (2008).
Hawkins, R. J. & McLeish, T. C. B. Coupling of global and local vibrational modes in dynamic allostery of proteins. Biophys. J. 91, 2055–2062 (2006).
Panjkovich, A. & Daura, X. Exploiting protein flexibility to predict the location of allosteric sites. BMC Bioinformatics 13, 273 (2012).
Andersen, O. S. Perspectives on: Ion selectivity. J. Gen. Physiol. 137, 393–395 (2011).
Corry, B. & Chung, S.-H. Influence of protein flexibility on the electrostatic energy landscape in gramicidin A. Eur. Biophys. J. 34, 208–216 (2005).
Noskov, S. Y., Bernèche, S. & Roux, B. Control of ion selectivity in potassium channels by electrostatic and dynamic properties of carbonyl ligands. Nature 431, 830–834 (2004).
Ngo, V., Stefanovski, D., Haas, S. & Farley, R. A. Non-equilibrium dynamics contribute to ion selectivity in the KcsA channel. PLoS One 9, (2014).
Napolitano, L. M. R. et al. A structural, functional, and computational analysis suggests pore flexibility as the base for the poor selectivity of CNG channels. Proc. Natl. Acad. Sci. USA 112, E3619–28 (2015).
Stevenson, P. et al. Visualizing KcsA conformational changes upon ion binding by infrared spectroscopy and atomistic modeling. J. Phys. Chem. B 119, 5824–5831 (2015).
Woods, K. N., Pfeffer, J., Dutta, A. & Klein-Seetharaman, J. Vibrational resonance, allostery, and activation in rhodopsin-like G protein-coupled receptors. Sci. Rep. 6, 1–17 (2016).
Braun, C. J. et al. Viral potassium channels as a robust model system for studies of membrane-protein interaction. Biochim. Biophys. Acta 1838, 1096–1103 (2013).
Jeanniard, A. et al. Towards defining the chloroviruses: a genomic journey through a genus of large DNA viruses. BMC Genomics 14, 158, https://doi.org/10.1186/1471-2164-14-158 (2013).
Papworth, C., Bauer, J. C., Braman, J. & Wright, D. Site-directed mutagenesis in one day with >80% efficiency. Strategies 9, 3–4 (1996).
Katzen, F. et al. Insertion of membrane proteins into discoidal membranes using a cell-free protein expression approach. J. Prot. Res. 7, 3535–3542 (2008).
Winterstein, L.-M. et al. Reconstitution and functional characterization of ion channels from nanodiscs in lipid bilayers. J. Gen. Physiol. 150, 637–646 (2018).
Braun, C. J., Baer, T., Moroni, A. & Thiel, G. Pseudo painting/air bubble technique for planar lipid bilayers. J. Neurosci. Methods 233, 13–17 (2014).
Heinemann, S. H. & Sigworth, F. J. Open channel noise. VI. Analysis of amplitude histograms to determine rapid kinetic parameters. Biophys. J. 60, 577–587 (1991).
Bordoli, L. et al. Protein structure homology modeling using SWISS-MODEL workspace. Nat. Protoc. 4, 1–13 (2009).
Pettersen, E. F. et al. UCSF Chimera–a visualization system for exploratory research and analysis. J. Comput. Chem. 25, 1605–1612 (2004).
The work has been supported by the Deutsche Forschungsgemeinschaft (HA 712/14-3 and SCHR 1467/1-1) and the European Research Council (NoMAGIC) under Grant Agreement No 695078. The authors declare no competing financial interests. We thank Simon Bernèche, Chris Miller and Axel Scheidig for helpful discussions.
The authors declare no competing interests.
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Rauh, O., Hansen, U.P., Scheub, D.D. et al. Site-specific ion occupation in the selectivity filter causes voltage-dependent gating in a viral K+ channel. Sci Rep 8, 10406 (2018). https://doi.org/10.1038/s41598-018-28751-w
Distinct lipid bilayer compositions have general and protein-specific effects on K+ channel function
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