Large-conductance (BK-type) Ca2+-activated potassium channels are activated by membrane depolarization and cytoplasmic Ca2+. BK channels are expressed in a broad variety of cells and have a corresponding diversity in properties. Underlying much of the functional diversity is a family of four tissue-specific accessory subunits (β1–β4). Biophysical characterization has shown that the β4 subunit confers properties of the so-called “type II” BK channel isotypes seen in brain. These properties include slow gating kinetics and resistance to iberiotoxin and charybdotoxin blockade. In addition, the β4 subunit reduces the apparent voltage sensitivity of channel activation and has complex effects on apparent Ca2+ sensitivity. Specifically, channel activity at low Ca2+ is inhibited, while at high Ca2+, activity is enhanced. The goal of this study is to understand the mechanism underlying β4 subunit action in the context of a dual allosteric model for BK channel gating. We observed that β4's most profound effect is a decrease in Po (at least 11-fold) in the absence of calcium binding and voltage sensor activation. However, β4 promotes channel opening by increasing voltage dependence of Po-V relations at negative membrane potentials. In the context of the dual allosteric model for BK channels, we find these properties are explained by distinct and opposing actions of β4 on BK channels. β4 reduces channel opening by decreasing the intrinsic gating equilibrium (L0), and decreasing the allosteric coupling between calcium binding and voltage sensor activation (E). However, β4 has a compensatory effect on channel opening following depolarization by shifting open channel voltage sensor activation (Vho) to more negative membrane potentials. The consequence is that β4 causes a net positive shift of the G-V relationship (relative to α subunit alone) at low calcium. At higher calcium, the contribution by Vho and an increase in allosteric coupling to Ca2+ binding (C) promotes a negative G-V shift of α+β4 channels as compared to α subunits alone. This manner of modulation predicts that type II BK channels are downregulated by β4 at resting voltages through effects on L0. However, β4 confers a compensatory effect on voltage sensor activation that increases channel opening during depolarization.

Introduction

BK channels are members of the voltage-dependent potassium channel family that are activated by membrane depolarization as well as increases in cytoplasmic Ca2+. These two stimuli appear to open the channel's gate via allosteric mechanisms (Horrigan and Aldrich, 1999; Horrigan et. al, 1999; Rothberg and Magleby, 1999, 2000; Horrigan and Aldrich, 2002; for review see Rothberg, 2004). Voltage sensor activation and Ca2+ binding act independently, in an energetically additive fashion, to stabilize the channel's open conformation; as [Ca2+] is increased, less membrane depolarization is required to open the channel (Cox et al., 1997a; Cui et al., 1997). In different cell types, these channels display diverse functional properties, despite having a pore-forming subunit that is encoded by only a single gene (slo or KCNMA). Numerous mechanisms contribute to BK channel functional diversity, including alternative splicing, channel phosphorylation, and assembly with a family of four accessory subunits, β1–β4 (Stockand and Sansom, 1998; Xie and McCobb, 1998; Fettiplace and Fuchs, 1999; Schubert and Nelson, 2001; Fury et al., 2002; Orio et al., 2002).

The accessory β4 subunit is a component of neuronal BK channels and confers properties mediating the so-called type II BK channels. These channels were originally identified in bilayer recordings from synaptosomal membrane preparations from brain (Reinhart et al., 1989, 1991; Reinhart and Levitan, 1995; Behrens et al., 2000; Brenner et al., 2000; Meera et al., 2000; Weiger et al., 2000; Lippiat et al., 2003). Type II BK channels have slow gating kinetics, decreased sensitivity to Ca2+ compared with type I channels, and are insensitive to block by charybdotoxin, consistent with the properties of BK channels coexpressed with the β4 subunit in heterologous cells (Reinhart et al., 1989; Reinhart et al., 1991; Reinhart and Levitan, 1995; Behrens et al., 2000; Brenner et al., 2000; Meera et al., 2000; Weiger et al., 2000; Lippiat et al., 2003). β4 knockout mice display abnormal neuronal firing properties and temporal lobe seizures, indicating that the gating properties conferred by the β4 subunits are essential to normal neuronal function (Brenner et al., 2005).

More detailed analysis of BK channel β4 subunit has been performed by coexpression of the cloned channels in heterologous expression systems. The β4 subunit was proposed to be a “downregulator of BK channels” due to dramatic slowing of activation and a positive voltage shift of the conductance–voltage relationship (Weiger et al., 2000). However, although β4 reduces BK channels opening at low Ca2+, it increases channel opening at high Ca2+ (Brenner et al., 2000; Ha et al., 2004). In addition, the β4 subunit reduces the voltage dependence (slope) of the macroscopic conductance–voltage (G-V) relationship. These properties are unique among the β subunit family members and the mechanisms underlying these effects are not known.

Here we provide a detailed analysis of the functional properties of BK α+β4 subunit channels. To understand how the β4 subunit modulates BK channels we have employed an allosteric modeling framework for BK channels (Horrigan and Aldrich, 2002), which enables us to ascribe kinetic changes to specific gating transitions. Our results demonstrate that β4 subunit effects can be accounted for by two opposing actions: β4 inhibits BK channel activation mainly by increasing the energetic barrier to opening by decreasing L0. This effect is countered by a negative voltage shift in voltage sensor activation for channels in the open state (parameter Vho in the model) and an increase in the allosteric coupling of Ca2+ binding to channel opening (parameter C in the model).

Materials And Methods

Channel Expression

Experiments were performed with the mouse α subunit cDNA expression vector in pcDNA3 (GenBank/EMBL/DDBJ accession no. MMU09383), and mouse β4 in the Invitrogen vector pcDNA3.1Hygro(+). Expression constructs were transfected at a ratio of 1:10 α to β4 subunit using 2–3 μg total DNA and 10 μl lipofectamine reagent per 35 mm dish of HEK293 cells. After 5 h of incubation, the cells were replated on glass coverslips and analyzed by electrophysiology for the following 1–3 d. GFP expression from cotransfection (0.2 μg) of the CLONTECH Laboratories, Inc. EGFP-N1 vector was used to identify channel-expressing cells.

Patch Clamp Recording

Macropatch recordings were made using the excised inside-out patch clamp configuration. To limit series resistance errors, currents 5 nA or less were used for steady-state G-V. For 0 Ca2+ experiment determination of limiting Po, larger currents were used but estimates of maximal conductance was determined at high Ca2+ and using small tail-current voltage steps. Experiments were performed at 22°C. Data were sampled at 10–30-μs intervals and low-pass filtered at 8.4 kHz using the HEKA EPC8 four-pole bessel filter. Data were analyzed without further filtering. Leak currents were subtracted after the test pulse using P/5 negative pulses from a holding potential of −120 mV. In the presence of β4 at ≥60 μM Ca2+, leak subtraction was not performed. Patch pipettes (borosilicate glass VWR micropipettes) were coated with Sticky Wax (Kerr Corp.) and fire polished to ∼1.5–3 MΩ resistance.

The external recording solution (electrode solution) was composed of 20 mM HEPES, 140 mM KMeSO3, 2 mM KCl, 2 mM MgCl2, pH 7.2. Internal solutions were composed of a pH 7.2 solution of 20 mM HEPES, 140 mM KMeSO3, 2 mM KCl, and buffered with 5 mM HEDTA and CaCl2 to the appropriate concentrations to give 1.7, 7, and 18.5 μM buffered Ca2+ solutions. Higher Ca2+ solutions were buffered with 5 mM NTA. Low Ca2+ solutions (0.3 μM and 0 Ca2+) were buffered with 5 mM EGTA and Ba2+ was chelated with 40 μM (+)-18-crown-6-tetracarboxylic acid (Cox et al., 1997b). Conductance–voltage (G-V) relationships were obtained using a test pulse to positive potentials followed by a step to a negative voltage (−80 at low Ca2+, −120 at high Ca2+), and then measuring instantaneous tail current 200 μs after the test pulse. V1/2 and Q values were determined by fitting G-V curves to Boltzmann function (

\(G{=}G_{\mathrm{max}}{\{}1/(1{+}e^{{-}(V{-}\mathrm{V}_{1/2})QF/RT)}{\}}\)
⁠) and then normalized to the maximum of the fit. At 0 and 0.3 μM Ca2+, where maximum conductance could not be obtained in the presence of β4, conductance was normalized to maximal conductance at high Ca2+.

Single Channel Analysis

Single channel opening events were obtained from patches containing one to hundreds of channels. Recordings were of 20 s to hundreds of seconds duration. Analysis was performed using TAC and TACFIT programs (Bruxton Corporations). NPo was determined using either all-point amplitude histogram or by event detection using a 50% amplitude criteria. The probability (Pk) of occupying each open level (k) gives rise to NPo:

\(NP_{o}{=}{\sum}kP_{k}\)
⁠. Po was then determined by normalizing NPo values by channel number (N). N was obtained from the instantaneous tail current amplitude (−80 mV) during maximal opening at saturating [Ca2+] divided by the unitary conductance for each channel at the tail voltage. β4 caused a reduced single channel conductance at negative voltages for BK channels as compared with α subunits alone. At −80 mV the conductance was 175 ± 7 pS for α+β4, and 250 ± 13 pS for α alone. Positive voltages did not show a significant change in single channel conductance. At +80 mV, single channel current was 214 ± 7 pS for α+β4 and 225 ± 14 pS for α alone.

Results

Effects of β4 on Channel Steady-state G-V Relations and Po

BK channel properties in the absence of the β4 subunit (α alone) or in the presence of saturating amounts of β4 (α+β4) were characterized in transiently transfected HEK293 cells. Currents were recorded in the inside-out configuration over a range of [Ca2+] at the intracellular face of the membrane patch ([Ca2+]i). Fig. 1 A shows representative current traces of α alone and α+β4 recorded at 7 μM [Ca2+]i. In Fig. 1 B, mean steady-state conductance–voltage (G-V) relations are plotted as a function of [Ca2+]i. To better quantify effects of β4 on channel steady-state gating properties, G-V curves of individual recordings were fit with single Boltzmann functions (see MATERIALS AND METHODS) to derive the voltage for half-maximal activation (V1/2) and equivalent gating charge Q (slope of G-V relationship or “voltage dependence”). Mean V1/2 and Q values for α alone and α+β4 as a function of [Ca2+]i are listed in Table I and plotted in Fig. 1 (C and D), respectively. Our data, consistent with previous results obtained with heterologous expression in Xenopus oocytes, show that the β4 subunit affects the steady-state conductance–voltage relationship (Brenner et al., 2000; Ha et al., 2004). At [Ca2+] <18 μM, V1/2 is shifted toward more depolarized voltages in the presence of β4 (Fig. 1 C, inset). However, at [Ca2+] >18 μM, V1/2 is shifted toward more negative voltages in the presence of β4. In addition, we also saw that at all [Ca2+], β4 has a dramatic effect on the apparent voltage dependence of BK channels (Fig. 1 D). This is particularly prominent at [Ca2+] <1.7 μM and becomes incrementally more steep as [Ca2+] is increased.

The relative change in the V1/2 by β4 is between −26 and +90 mV, depending on the calcium concentration (Fig. 1 C, inset). However, the V1/2 may not reflect the relative changes in Po at physiological voltages. To determine effects on open probability, we measured channel Po in 300 nM [Ca2+] at the physiological voltages of −100 to +20 mV. The results indicate that at negative voltages, α+β4 channels show a large reduction in Po as compared with α subunits alone (Fig. 1 E). For example, at −80 mV α+β4 channels have a 4.3-fold reduction in Po relative to α subunits alone (average Po α+β4 is 3.5 e−7 ± 1.9 e−7, α alone is 1.5 e−6 ± 3.3 e−7). However, at +20 mV, there is no significant difference in Po between channel types (Fig. 1 E).

Effects of β4 on Gating through the Low Affinity Ca2+ Binding Site

In considering the calcium-dependent effect of β4 on the V1/2, it is important to note that BK channels are modulated over a wide range of Ca2+, from the submicromolar range up to ∼1 mM. The fact that Ca2+ does not appear to saturate channel activation (in the absence of β4) is attributed to the existence of both high and low affinity Ca2+ binding sites (Zhang et al., 2001; Shi et al., 2002). This is apparent in Fig. 1 C (open symbols) as increasing Ca2+ shifts the V1/2 strongly at [Ca2+]i <60 μM, consistent with activation at a high affinity site, then shifts the V1/2 weakly at [Ca2+]i >100 μM, consistent with activation at a low affinity site.

The β4 subunit promotes a negative voltage shift of the G-V curve only at high [Ca2+] (Fig. 1 C, inset). A possible explanation for this is that β4 may specifically affect Ca2+ binding to low affinity sites to promote activation at high calcium; either its affinity or coupling between Ca2+ binding and gating. We examined whether the β4 subunits promote activation through low affinity Ca2+ binding sites by measuring activation by millimolar concentrations of Mg2+, which acts only at low affinity sites (Shi et al., 2002). If the leftward shift in V1/2 induced by the β4 subunits is due to increased activation at the low affinity site, then addition of Mg2+ should produce a larger leftward shift in the presence of β4 compared with α alone channels.

Steady-state G-V relations with and without 10 mM Mg2+ were obtained in the presence and absence of β4. Fig. 2 shows currents activated in 60 μM Ca2+, (Fig. 2 A, left, and Fig. 2 B, open symbols) and then channels are further activated through low affinity sites with 10 mM Mg2+ (Fig. 2 A, right, and Fig. 2 B, closed symbols). Mg2+ actually yielded a smaller G-V shift for α+β4 channels (by −69 mV) compared with α alone (by −96 mV), suggesting that β4 does not increase gating through Ca2+ binding at the low affinity site. A flaw of this interpretation is that inferring effects of Ca2+ binding to the low affinity sites using 10 mM Mg2+ may be inappropriate in the presence of Ca2+. At 60 μM Ca2+, it is possible that 10 mM Mg2+ can compete with Ca2+ for the low affinity site and therefore confer some inhibitory effects on gating. To rule out such possibility, effect of β4 on G-V shift by 10 mM Mg2+ was also examined at 0 Ca2+. Again, 10 mM Mg2+ produced a smaller shift in V1/2 for α+β4 channels compared with α alone (−64 vs. −96 mV, respectively; Fig. 2 C). Together, these results suggest that activation at high Ca2+ cannot be explained by changes involving the low-affinity Ca2+ binding site.

Understanding Effects of β4 on Channel Gating in the Context of an Allosteric Model

BK channel gating can be understood in terms of a dual allosteric model in which activation of a voltage sensor and a Ca2+ sensor each facilitate opening of the channel (Scheme 1) (Rothberg and Magleby, 1999; Horrigan and Aldrich, 2002).

In this model, channel opening is governed by three equilibrium constants, L (closed-to-open transition), J (voltage sensor activation), K (Ca2+ binding), and three allosteric factors D (coupling of voltage sensor movement to channel opening), C (coupling of Ca2+ binding to opening), and E (interaction between Ca2+ binding and voltage sensor movement). Detailed descriptions of these parameters are listed in Table II. Open probability can be described by Eq. 1:

 
\[P_{o}{=}\frac{1}{1{+}\frac{(1{+}J{+}K{+}JKE)^{4}}{L(1{+}KC{+}JD{+}JKCDE)^{4}}}.\]
(1)

To understand the mechanism underlying β4 modulation of the channel, we examined how individual gating parameters are altered by β4. Our experimental approach was to measure Po under conditions that reduce the number of occupied states and thereby constrain a number of gating parameters. For example, to observe effects on voltage dependence, we measured Po-V relations in the virtual absence of calcium. To observe effects of β4 on calcium dependence, we measured Po-V relations at very negative voltages where voltage sensors are in the resting state. These experiments are presented below. The remaining gating parameters were then estimated by fitting all

\(\mathrm{P}_{\mathrm{o}[\mathrm{v},{\,}\mathrm{Ca}^{2{+}}]}\)
data using Eq. 1.

The β4 Subunit Shifts Voltage Sensor Activation to Negative Voltages and Increases the Intrinsic Energetic Barrier for Channel Opening

Our first aim was to measure β4 effects on the closed-to-open equilibrium and its voltage dependence (L0 and zL, respectively). Based on the dual allosteric model (Horrigan and Aldrich, 2002) this can be accomplished by measuring Po-V relations in the virtual absence of Ca2+ (Horrigan and Aldrich, 1999). This effectively reduces the number of occupied states to 10 (Fig. 3 A, Sub-Scheme 1a) and Po is determined by the equilibrium of intrinsic gating, L (where L = L0exp(zLV/kT)), voltage sensor activation, J, and the allosteric interaction between them, D (Horrigan et al., 2002):

 
\[P_{o}{=}\frac{1}{1{+}\frac{(1{+}J)^{4}}{L(1{+}DJ)^{4}}}.\]
(2)

A simulated Po-V relation predicted by Eq. 2 is shown in Fig. 3 A (right). At very negative membrane potentials, the slope of the Po-V relation is very shallow (limiting slope), reflecting the weak voltage dependence (zL) of the closed-to-open transition independent of voltage sensor movement. This is followed by a steeper voltage dependence at high voltages where voltage sensors start to activate and contribute to voltage sensor–dependent channel gating. By confining our analysis to very negative voltages, channel occupancy can be further reduced to two states, C0 and O0 (Fig. 3 A, Sub-Scheme 1b). Because J is small (J ≪ 1/D), Eq. 1 reduces to

 
\[P_{o}{=}\frac{L}{1{+}L}.\]
(3)

Where Po is also small

\((\mathrm{P}_{\mathrm{o}}{<}0.01),{\,}\mathrm{L}{\ll}1,\)

 
\[P_{o}{=}L{=}L_{0}{\,}\mathrm{exp}\left(\frac{z_{L}V}{kT}\right).\]
(4)

Thus parameters describing channel intrinsic gating properties (L0 and zL) can be estimated by fitting logPo-V relation at very negative potentials using Eq. 4. The slope of the fit is a function of voltage dependence of the closed-to-open transition (zL), and the 0 mV value of the fit is a measure of the closed-to-open equilibrium of intrinsic channel gating (L0).

To evaluate effects of β4 on channel intrinsic gating parameters (i.e., independent of Ca2+ or voltage sensor activation) using Eq. 4, BK currents were measured in 0 Ca2+ at negative membrane potentials. Because channel open probabilities are very low under these conditions, recordings were obtained from patches containing hundreds of channels and analyzed using single-channel analysis techniques to estimate Po (the number of channels in each patch was estimated by measuring the maximal current amplitude at higher Ca2+ and dividing by the unitary current amplitude, see MATERIALS AND METHODS). Examples of recordings in the absence and presence of β4 are displayed in Fig. 3 B.

In the presence of β4, channel openings are less frequent but display longer durations, consistent with previous observations (Ha et al., 2004). Mean logPo-V relations (between −80 and +100 mV) are displayed in Fig. 3 C. These data demonstrate effects of β4 on two aspects of channel gating. First, although the slope of logPo-V relation shows a clear decrease for the α alone channels at around +30 mV, there is little change in slope for the α+β4 channels over this voltage range (+70 through −80 mV). Possible explanations are either that (a) for α+β4 channels, zL is increased, and thus comparable to the voltage dependence of opening at higher voltages (that involves voltage sensor activation), or (b) β4 does not effect zL, but we could not estimate zL because voltage sensor activation occurs at voltages more negative than for α alone channels. It is difficult to propose a plausible physical mechanism that could account for an increase in zL that would not also dramatically alter voltage dependence of Po at high voltages. Therefore, we hypothesize that β4 shifts activation voltage for open-channel voltage sensors (Vho) to membrane potentials more negative than −80 mV. Direct measurements of zL below −80 mV at 0 Ca2+ was not feasible because channel openings fall below our level of detection. However, this hypothesis is supported by measurement of zL at high Ca2+, as discussed below.

Our data also suggest that β4 decreases the channel's intrinsic equilibrium for opening (L0). L0 value for α alone channels was estimated by fitting Po-V relations between −100 and −70 mV (at limiting slope) using Eq. 4 and the estimated zL value of 0.3 e0. L0 for the α alone channel is estimated to be 1.6 × 10−6 (Fig. 3 D). In the presence of β4, we did not reach the membrane potential where contribution of voltage sensors can be ignored. Measuring Po below −80 mV is technically not feasible because channel openings for α+β4 are too few to get estimates of Po (Po < 1 e−8). Therefore, we estimated an upper limit for the closed-to-open equilibrium (L0) using the mean Po value at −80 mV and zL value of 0.3 e0 (Fig. 3 D). The estimated upper limit for L0 in the presence of β4 is 1.4 × 10−7, suggesting that β4 decreases the equilibrium constant of the closed-to-open transition by at least 11-fold.

Voltage Dependence of the Closed–Open Transition (zL) Is Not Altered by β4

We were able to evaluate effects of β4 on zL, the gating parameter that describes the voltage dependence of the closed-to-open transition, in the presence of Ca2+. Ca2+ increases the Po even in the absence of voltage sensor activation, which makes it feasible to obtain Po-V relations at the limiting slope and directly estimate zL. Based on the dual-allosteric model (Horrigan and Aldrich, 2002), Ca2+ should not change the voltage dependence of the closed-to-open transition. As illustrated in Fig. 4 A (Sub-Scheme 1c), at very low voltages, where voltage sensors remain in resting states, the number of occupied state reduces to 10 and Po is described as

 
\[P_{o}{=}\frac{L(1{+}KC)^{4}}{L(1{+}KC)^{4}{+}(1{+}K)^{4}}{=}\frac{L\left(\frac{1{+}KC}{1{+}K}\right)^{4}}{L\left(\frac{1{+}KC}{1{+}K}\right)^{4}{+}1}.\]
(5)

When Po is small

\((\mathrm{P}_{o}{\ll}0.01),{\,}L\left(\frac{1{+}KC}{1{+}K}\right)^{4}{\ll}1,\)
Eq. 5 reduces to

 
\[P_{o}{=}L\left(\frac{1{+}KC}{1{+}K}\right)^{4}{=}L_{0}\left(\frac{1{+}KC}{1{+}K}\right)^{4}\mathrm{exp}\left(\frac{z_{L}V}{kT}\right).\]
(6)

Po-V relations predicted by the gating scheme is illustrated by simulated Po-V relations at 0 and 100 μM [Ca2+] (Fig. 4 A, right). By using Eq. 6 to fit Po-V at very negative membrane potentials in the presence of [Ca2+] (Fig. 4 A), zL can be obtained since the higher Po makes measurements more feasible.

To estimate zL in the absence and presence of β4, we measured Po in the presence of 0–100 μM [Ca2+] at decreasing membrane potentials. Examples of recordings at 100 μM Ca2+ at very negative membrane potentials are shown in Fig. 4 B. In a portion of recordings, logPo-V relation appeared to have reached the “limiting slope”. Fig. 4 C illustrates how zL was estimated using such recordings. The regions of the log(Po)-V relations where voltage dependence of Po is clearly reduced were fit with Eq. 6 to estimate zL. Mean zL values for α subunit alone at different [Ca2+] are summarized in Fig. 4 D. Consistent with the dual allosteric model (Horrigan and Aldrich, 2002), zL value estimated at various [Ca2+] appear to be similar. The mean of all estimates of zL for the α alone channels was 0.30 ± 0.02 e0 (n = 26). The limiting slope was reached in a much smaller portion of α+β4 recordings, especially at low [Ca2+] (Fig. 4 D). Estimates of zL at 18.5 and 100 μM Ca appeared to be better constrained than at lower Ca2+. The mean zL for α+β4 channels was 0.31 ± 0.03 e0 (n = 21). When only the best constrained data (18.5 and 100 μM) were included, the mean zL was 0.29 ± 0.03 e (n = 10). In conclusion, β4 does not appear to alter zL, voltage dependence associated with channel's closed-to-open transition.

Effect on Ca2+ Sensitivity

Po-V relations at the limiting slope in the presence of Ca2+ can be used to assess effects of β4 on Ca2+-dependent gating (Horrigan and Aldrich, 2002). As discussed above, when Po is low (<0.01), Eq. 5 reduces to Eq. 6. We can define L0′ as the closed-to-open equilibrium with the allosteric contribution of calcium binding (in the absence of voltage sensor activation):

 
\[L_{0}{^\prime}{=}L_{0}\left(\frac{1{+}KC}{1{+}K}\right)^{4}.\]
(7)

Then Po changes in the absence of voltage sensor activation becomes

 
\[P_{o}{=}\left(L_{0}\left(\frac{1{+}KC}{1{+}K}\right)^{4}\right)\mathrm{exp}\left(\frac{z_{L}V}{kT}\right){=}L_{0}{^\prime}\mathrm{exp}\left(\frac{z_{L}V}{kT}\right).\]
(8)

In the presence of Ca2+, Po-V measured at limiting slope can be fitted by Eq. 8 to estimate L0′. This is similar to the approach for evaluating L0 (Fig. 3 D). L0′-[Ca2+] relations can then be fitted by Eq. 7 to estimate β4 effects on calcium-dependent parameters, Kc and C.

Mean logPo-V relations for the α alone and α+β4 channels are presented in Fig. 5 A. For the α alone channels, the limiting slopes of the logPo-V relations were reached and fitted with Eq. 8 to estimate L0′. Log L0′ are plotted as a function of [Ca2+] (Fig. 5 B). Fitting log(L0′) (from mean data) vs. [Ca2+] with Eq. 7 yielded L0 = 1.7 × 10−6 ± 5 × 10−7, Kc = 13 ± 3 μM and C = 10 ± 1. These values are similar to previous estimates of the α alone channels based on the dual-allosteric model (L0 = 9.8 × 10−7, Kc = 11 μM, and C = 8; Horrigan and Aldrich, 2002).

For the α+β4 channels, we again observe a negative shift in the voltage sensor activation (Vho). However, the limiting slope of logPo-V relations were reached in a small percentage of recordings that allow estimation of zL (Fig. 4 C), the limiting slope of logPo-V relation was not reached in the majority of the patches (Fig. 4 D and Fig. 5 A). This is reflected in the logPo-V plot in Fig. 5 A (right) where only the foot of the data points show a reduction in voltage dependence. Although L0′ could not be obtained directly, nevertheless high limits for L0′ at different [Ca2+] were determined by mean Po value measured at the lowest membrane potentials using Eq. 8 and the mean zL value of 0.3 e0. The results show a plot that can be regarded as upper limits of L0′ for the α+β4 channels (Fig. 5 B). Interestingly, L0′ values for α+β4 were smaller than L0′ for the α alone channels, at all [Ca2+]. This is an important finding in light of the fact that, at high Ca2+, β4 causes an increase in Po at higher voltages (negative shift of V1/2 at high calcium, Fig. 1 C). These findings suggest that Ca2+ binding (through high or low affinity sites) alone is insufficient to cause the negative G-V shift conferred by β4 in high Ca2+. By default, aspects of β4 modulation of voltage sensor activation must contribute to the leftward G-V shift at high Ca2+.

Effects of β4 in the Context of an Allosteric Model

The above analysis directly examined effects of β4 on several aspects of BK channel gating. Our analysis of open probability at limiting slope suggests that β4 increases the energetic barrier for channel opening, and causes a negative shift in the activation of voltage sensors for open channels. To understand these effects in a comprehensive framework, and whether other aspects of gating are affected by β4, families of G-V curves as well Po-V relations obtained at low voltages were fit with the dual allosteric model (Scheme 1; Horrigan and Aldrich, 2002).

There are seven free parameters in the allosteric model (Table II). For α alone channels, four of these parameters were constrained based on analysis of our experimental data. These parameters (and range of values imposed) were zL (0.3 e), L0 (1.7 × 10−6), Kc (13 μM), and Ko (1.3 μM). The remaining parameters (zJ, Vhc, Vho, and E) were allowed to vary freely. Although a range of parameters produce satisfactory fits for the G-V curves, we found only one set of parameters that could also reproduce Po-V data measured at very negative voltages. These are shown in Table III. Simulated Po with parameters in Table III reproduces reasonably well the α alone G-V curves over a wide range of Ca2+ (from nominally 0 through 100 μM; Fig. 6 A) as well as Po at low voltages (Fig. 6 B), the V1/2 vs. [Ca2+] relation (Fig. 6 G), the Q vs. [Ca2+] relation (Fig. 6 H), and the Ca2+-dependent shift in Po in the absence of voltage sensor activation (Fig. 6 I). These parameters are similar to previously reported for the α alone channels (Horrigan and Aldrich, 2002).

To estimate gating parameters in the presence of β4, we fit G-V data and low voltage Po-V relations from α+β4 channels to the dual allosteric model (Horrigan and Aldrich, 2002). Based on our analysis of α+β4 channel gating at low Po, zL was constrained to be 0.3 e0. Consistent with the experimental measurements in 0 calcium, the best fit (α+β4_a, Table III) suggests that major effects of β4 include decrease of L0 (46 fold) and a −75 mV shift of voltage sensor activation (Vho) relative to α subunits alone. In addition, the closed channel voltage sensor equilibrium (Vhc) is shifted to a similar extent (−77 mV), resulting in a relatively small change in voltage-dependent allosteric coupling (D). The fit indicates that there is a threefold decrease in Ca2+ binding affinity in the closed channel (Kc) with a smaller reduction in the open channel, resulting in an increase in calcium-dependent allosteric coupling (C). Finally, there is a small decrease in the direct allosteric coupling between Ca2+ binding and voltage sensor activation (E). Fit α+β4_a nicely reproduces the G-V data (Fig. 6, C and G) as well as the low voltage Po-V relations (Fig. 6 D) and the Q vs. [Ca2+] relations (Fig. 6 H).

As expected, because measured logL0′ are upper limits of the expected values, the model parameters predict a curve that falls below the α+β4 measurements (Fig. 6 I). This highlights the importance of the low voltage, single-channel Po measurements in constraining the model. To further illustrate this, the macroscopic G-V data alone was used to fit Scheme 1 with zL again fixed to 0.3 e0. Although the best fit using the macroscopic G-V data alone (α+β4_b, Table III) predicts the macroscopic G-V data quite well (Fig. 6, E, G, and H), the parameters poorly predict Po-V relations at negative voltage and low calcium (Fig. 6 F), and the predicted logL0′ values are larger than the measured upper limits in 0 calcium (Fig. 6 I).

The Effects of β4 on L0 and Vho Are Robust

Our best fit of the α+β4 data, α+β4_a, indicates that the major effects of β4 are a decrease in L0 and negative voltage shifts of voltage sensor equilibrium (Vho). To examine whether the kinetic parameters in α+β4_a are robust, we fixed L0 or Vho at increased or decreased values, and then refit the other parameters to see if compensatory changes could be made in other parameters that might result in an equivalent fit.

To test if the L0 value is robust, we obtained fits α+β4_c and α+β4_d (Table III) by fixing L0 at values three times larger or smaller, respectively, than that predicted by α+β4_a. When L0 is three times larger, the fit predicts the G-V data quite well (α+β4_c; Fig. 7 B, left), but does not predict the low voltage Po-V relations at low calcium as well as α+β4_a (Fig. 7 B, right ). When L0 is three times smaller (α+β4_d), Vho is shifted in the negative direction to compensate. The fit to the low voltage Po-V relations is improved relative to α+β4_c (Fig. 7 C), although it is not improved over α+β4_a.

To analyze the impact of shifting Vho on fitting the α+β4 data, Vho was fixed to a more positive value, resulting in α+β4_e (Fig. 7 D). This would correspond to a reduced contribution of voltage sensor activation to channel opening at negative voltages. Table III shows that the major compensatory effect is an increase in L0 and E, both of which would correspond to increased channel opening at negative voltages. Although the macroscopic G-V data is predicted fairly well (Fig. 7 D, left), the low voltage Po-V relations in low calcium are not predicted well (Fig. 7 D, right). In contrast, shifting Vho to more negative potentials as compared with α+β4_a (Fig. 7 E) allows fits that are comparable to α+β4_a. Because the negative shift of Vho has the effect of increasing Po at negative voltages, this is compensated for by a large decrease in the L0 value (to 1.6 e−9; Table III) and reduction in allosteric coupling between voltage sensor movement and calcium binding (E). Interestingly, the best fits (α+β4_a, α+β4_d, and α+β4_f) seem to constrain Vhc to around 110 mV (Table III), regardless of a negative shift of the Vho or a reduced L0. Consistent with this, we observed that a +50 or −50 mV shift in Vhc produces fits that deviate significantly from the G-V data (unpublished data).

This analysis demonstrate that low voltage Po-V relations constrain a model in which β4 mediates a negative shift of voltage sensor activation (Vho), and biases the intrinsic closed to open equilibrium (L0) toward the closed state. The data can be fit by L0 that is smaller than our estimates, if there is a corresponding negative shift in Vho. Independent of changes in these two parameters, this analysis indicates that β4 produces an increase in allosteric coupling to calcium binding (C), a reduction of closed channel calcium binding affinity (Kc), and a negative shift of Vhc.

Understanding Effects of β4 on BK Channels

BK channels α+β4 currents show a positive shift of the G-V relationship at low calcium and a negative shift of the G-V relationship at high calcium. In addition, the β4 subunit causes an apparent reduction in voltage dependence at low calcium. How do the changes in individual gating parameters altered by β4 confer α+β4 properties? To address this question, the α subunit steady-state properties were simulated and compared with simulations where individual β4 gating parameters are used to replace α subunit parameters. These are shown as individual changes in Figs. 8 and 9, and as additive changes in Fig. 10.

Effect on the Closed-to-Open Transition

Independent of voltage sensor movement and Ca2+ binding, BK channel opening is governed by an intrinsic energetic barrier (described by L0) that has a weak intrinsic voltage dependence (zL) (Horrigan and Aldrich, 2002). Data in Fig. 3 D suggest that the equilibrium constant L is significantly increased (at least by 11-fold) in the presence of β4. Our best fit indicates that the β4 subunit decrease (L0 from 1.7 × 10−6 for α alone to 3.7 × 10−8 for α+β4_a, approximately by 46-fold, indeed lower than our estimated upper limits (Fig. 3 D).

Effects of a 46-fold decrease in L0 are illustrated in Fig. 8. We first simulated G-V relations at various Ca2+ based on gating parameters for α (Table III) and obtained V1/2-[Ca2+] and Q-[Ca2+] relations by fitting simulated G-V curves with Boltzmann function (Fig. 8, A and B). To see how changes in L0 might affect BK channel gating, we simulated G-V curve using α parameters except for the L0, which is replaced by that of β4 L0 (Fig. 8, A and B). As expected, a 46-fold decrease in L0 by β4 creates a positive shift of the V1/2 at all [Ca2+] (Fig. 8 A, β4_L0). Interestingly, the effect of L0 also causes a significant decrease in the voltage dependence (Fig. 8 B).

Why does decreasing L0 cause a decrease in voltage dependence, particularly at submicromolar [Ca2+]? In the dual allosteric gating scheme (Scheme 1), voltage sensors are activated around a voltage range defined by Vho for open channels and Vhc for closed channels. Within this range (between Vho and Vhc), the energetic difference between voltage sensor activation in closed and open channel is greatest, thus allosteric coupling between voltage sensor activation and gating is the strongest, and Po is most voltage dependent (large Q). The effect of L0 or calcium positions Po-V curves along the voltage axis relative to Vho and Vhc and therefore affects the voltage dependence. This is illustrated in Po-V relations at two different [Ca2+] simulated with the parameter from α alone channels, in Fig. 8 C. Channel opening at 0 and 7 μM calcium falls approximately within this voltage range, and G-V curves show high voltage dependence (steep slope). Below and above these ranges, voltage sensors are either in the resting or activated state, respectively, and voltage-dependent channel openings are dependent on the weaker closed-to-open voltage dependence, zL. In contrast, data simulated using an L0 fixed at the value estimated for α+β4 channels (Fig. 8 D) resulted in channel openings at voltages more positive than Vhc for the 0 Ca2+ data. This resulted in a reduced voltage dependence (shallower slope). However, as higher calcium (≥7 μM) contributes significantly to channel gating, openings fall within the ranges where voltage sensors contribute to channel gating and we see a greater apparent voltage dependence.

By examining apparent Q vs. V1/2 (determined by fitting simulated data with Boltzmann equations; Fig. 8 E), we can see that the L0 affects Q mostly by shifting the V1/2 along the voltage axis. Where V1/2 is similar between α and β4_L0, the Q values are similar. At low [Ca2+], channel activation occurs at membrane potentials more depolarized than Vhc, causing a decrease in apparent voltage dependence (Q). This is more dramatic in the presence of β4, since the significant decrease in L0 requires much higher membrane potential to open the channels.

Effect on Ca2+ Dependence

The fits with Scheme 1 suggest that the α+β4 channels have a threefold reduction in affinity of Ca2+ in the closed state (Kc = 13 μM α alone; 44 μM α+β4) with little change in affinity of the open state (Ko = 1.3 α alone; 1.9 μM α+β4). Thus, the β4 subunit imparts an increase in the strength of allosteric coupling between Ca2+ binding and channel opening (C = 10 for α alone vs. 23 for α+β4). A reduced affinity and greater coupling to Ca2+ binding may contribute to the negative shift in the V1/2 at high Ca2+ (Fig. 9 A). It should be noted however, that the model predicts that effects on Ca2+ sensitivity alone are not sufficient to offset the increased L0, particularly at low Ca2+ (Fig. 9 A, open circles). This is consistent with Ca2+ experiments discussed previously (Fig. 5 B). In these experiments, we found that the contribution of calcium alone in the absence of voltage sensor activation does not impart sufficient energy to shift the V1/2 more negative to α subunit. As discussed below, left shift of voltage sensor activation (Vho) makes an important contribution to the negative shift of the V1/2.

Interestingly, effects on allosteric coupling to Ca2+ (C) appear to contribute to a slight reduction in apparent voltage sensitivity in high Ca2+ (Fig. 9 B). Increased Ca2+ coupling positions the V1/2 at 100 μM at approximately −60 mV, below the foot of voltage sensor activation (Vho is +25 mV for α, see Table III). These effects are predicted to reduce apparent voltage dependence at high calcium, as indeed we see for α+β4 channels (Fig. 1 D).

Effect on Voltage Dependence

Although the fits suggest that β4 does not alter zJ (0.56 e0 for α and 0.55 e0 for α+β4), it causes large shifts in the equilibrium of voltage sensor activation in both the open state (Vho = 25 mV α alone vs. −50 mV α+β4) and closed state (Vhc = 187 mV α alone vs. 110 mV α+β4). Although coupling between voltage sensor activation and gating (D) is slightly decreased by β4 (35 for α and 32 for α+β4), changing Vho and Vhc results in a significant negative shift of the G-V curves at [Ca2+] >7 μM, sufficient to compensate for the increased energetic barrier (L0) conferred by β4 (Fig. 9 C). It should be noted that the effect of changing Vho, besides shifting the G-V curves to more negative membrane potentials, also positions the G-V at a more optimal position relative to Vho and Vhc to increase the apparent voltage dependence (Fig. 9 D). The above results and recent findings by Bao and Cox (2005) illustrate another important prediction of the dual allosteric model: channel gating is regulated not only by the coupling factor D but also by the value of Vho and Vhc.

Analysis of the effects of α+β4 currents demonstrates that the change in properties contributed by the β4 subunit offset each other to produce moderate changes in the conductance–voltage relationship. A manner to consider these changes is to simulate the

\(\mathrm{P}_{\mathrm{o}[\mathrm{v},{\,}\mathrm{Ca}^{2{+}}]}\)
using the α subunit parameters, and compare these to simulated data where the α+β4 parameters are incrementally used to replace those of α subunit channels. This is shown in Fig. 10. The effect of β4 on the closed-to-open equilibrium, L, and coupling between gating and to voltage sensor movement, D, have opposing and parallel effects on the V1/2-[Ca2+] relations (Fig. 10, A and B). The decrease of L0 shifts the curve to positive potentials, and D has a compensatory shift to negative potentials at [Ca2+] >7 μM. Increased coupling between calcium binding and gating (C) further increases the slope of the V1/2 vs. [Ca2+] curve so that at high [Ca2+] the V1/2 is shifted to more negative membrane potentials relative to α subunits alone (Fig. 10 C). Model fits indicate that the β4 subunit reduces allosteric coupling between voltage sensor movement and calcium binding (E), which contributes to a positive shift of the V1/2 at high [Ca2+] (Fig. 10 D).

Discussion

Our analysis demonstrates that the β4 subunit alters several aspects of BK channel gating. In this respect, β4 is similar to the β1 subunit, which has been shown to modulate BK channels in a complex manner (Cox and Aldrich, 2000; Orio and Latorre, 2005). For the β4 subunit, we show that these are fairly dramatic effects on BK channel gating properties, particularly Vho and L0, that seem to offset one another to produce moderate changes in the conductance–voltage relationship at micromolar [Ca2+]. In many regards, this too is similar to changes observed with β1 subunits. β1 and β4 both mediate a negative voltage shift of open channel voltage sensor activation, Vho (Cox and Aldrich, 2000; Bao and Cox, 2005; Orio and Latorre, 2005). In addition, it appears that β1 and β4 both increase the energetic barrier to opening by reducing L0 (Orio and Latorre, 2005). This is somewhat controversial because a more recent study did not see an effect on L0 by β1 (Bao and Cox, 2005).

What underlies the negative voltage shift of the G-V relationship at high [Ca2+] that is often described as an “apparent increase in Ca2+ sensitivity”? Orio and Latorre attribute the apparent increase in Ca2+ sensitivity by β1 to a decrease in zJ (Orio and Latorre, 2005). Similar to predictions by Bao and Cox (2005) for the β1 subunit, our simulations indicate that the negative shift in Vho by β4 has the highest contribution to increase channel opening. A very important aspect of the dual-allosteric model is that energetic contributions of voltage sensors are not equivalent over the voltage axis. Although we did not see a dramatic change in voltage-dependent allosteric coupling factor D, the negative shift of voltage sensor activation (Vho) contributed significantly to increase Po. In this, the β4 and β1 are also similar (Bao and Cox, 2005).

Why would evolution alter so many properties of BK channels to produce a net effect on the V1/2 that appears relatively moderate, particularly at higher calcium concentrations? For instance, at [Ca2+] between 1.7 and 18 μM, the V1/2 is shifted by β4 to positive potentials ∼20 mV or less (Table I). At [Ca2+] >18 μM, there is a similar 10–30 mV negative shift. In considering the physiological role for BK α+β4 properties, one must consider the fact that the V1/2 value often does not reflect the open probabilities at physiological voltages, particularly at resting global [Ca2+] where the V1/2 is >100 mV. Instead, it may be more relevant to consider the changes in open probability in the physiological voltages between −80 and +20 mV. Although Po values can be low, opening of even a relatively few BK channels can nevertheless have profound effects on membrane voltage. For instance in vascular smooth muscle, activation of a cluster of BK channels near a Ca2+ spark site can hyperpolarize the membrane by 10–20 mV (Knot et al., 1998). For β4 subunits, which are predominantly expressed in neurons, the larger energetic barrier to opening (L0), would be expected to hold BK channels silent at resting voltages. However, the negative shift of the Vho means that voltage sensors are more easily activated following depolarization. Thus, appropriate with the concept that neurons respond to very transient changes in membrane potential, the opposing properties conferred by β4 subunits, increased energetic barrier to opening (L0) and a negative shift of voltage sensor activation (Vho), allow BK channels to activate in a switch-like, rather than graded, fashion. For instance, at 1.7 μM calcium and resting membrane voltage of −80 mV, α+β4 L0 confers a >10-fold lower Po than α subunits alone (Po α is 1.9 × 10−5, α+β4 1.6 × 10−6). However following depolarization to +20 mV, effects on Vho allow α+β4 BK channels to have a similar Po to that of α subunits alone (Po α is 4.0 × 10−3, α+β4 3.4 × 10−3). Indeed, recent findings that mutations resulting in gain of function of BK channels lead to seizure phenotypes (Du et al., 2005, Brenner et al., 2005) highlights the importance of holding BK channels silent until necessary.

The current study has focused on steady-state properties conferred by β4 subunits. Yet the β4 subunit has very profound effects on BK channel activation and deactivation kinetics that may be more physiologically important in neurons, where the β4 subunit appears to be enriched (Weiger et al., 2000). In central neurons, BK channels appear to have an important role in membrane repolarization following an action potential (Hu et al., 2001). Yet the β4 subunit slows the activation of BK channels to time scales that are incompatible with a role in shaping individual action potentials (tens to hundreds of milliseconds; Brenner et al., 2000). Further studies are warranted to understand how β4 effects on L0 and Vho mediate changes in gating kinetics.

Acknowledgments

We would like to acknowledge Dr. Frank Horrigan for advice and Dr. Jim Stockand for critical reading of the manuscript.

This work was supported by National Institutes of Health training grant HL04776-23 to B. Wang, National American Heart Association (AHA) grant 0335007N and Epilepsy Foundation of America grant to R. Brenner, and AHA, Texas Affiliate, grant 0265124Y to B.S. Rothberg.

Olaf S. Andersen served as editor.

References

References
Bao, L., and D.H. Cox.
2005
. Gating and ionic currents reveal how the BKCa channel's Ca2+ sensitivity is enhanced by its β1 subunit.
J. Gen. Physiol.
126
:
393
–412.
Behrens, R., A. Nolting, F. Reimann, M. Schwarz, R. Waldschutz, and O. Pongs.
2000
. hKCNMB3 and hKCNMB4, cloning and characterization of two members of the large-conductance calcium-activated potassium channel β subunit family.
FEBS Lett.
474
:
99
–106.
Brenner, R., Q.H. Chen, A. Vilaythong, G.M. Toney, J.L. Noebels, and R.W. Aldrich.
2005
. BK channel β4 subunit reduces dentate gyrus excitability and protects against temporal lobe seizures.
Nat. Neurosci.
8
:
1752
–1759.
Brenner, R., T.J. Jegla, A. Wickenden, Y. Liu, and R.W. Aldrich.
2000
. Cloning and functional characterization of novel large conductance calcium-activated potassium channel β subunits, hKCNMB3 and hKCNMB4.
J. Biol. Chem.
275
:
6453
–6461.
Cox, D.H., and R.W. Aldrich.
2000
. Role of the β1 subunit in large-conductance Ca2+-activated K+ channel gating energetics. Mechanisms of enhanced Ca2+ sensitivity.
J. Gen. Physiol.
116
:
411
–432.
Cox, D.H., J. Cui, and R.W. Aldrich.
1997
a. Allosteric gating of a large conductance Ca-activated K+ channel.
J. Gen. Physiol.
110
:
257
–281.
Cox, D.H., J. Cui, and R.W. Aldrich.
1997
b. Separation of gating properties from permeation and block in mslo large conductance Ca-activated K+ channels.
J. Gen. Physiol.
109
:
633
–646.
Cui, J., D.H. Cox, and R.W. Aldrich.
1997
. Intrinsic voltage dependence and Ca2+ regulation of mslo large conductance Ca-activated K+ channels.
J. Gen. Physiol.
109
:
647
–673.
Du, W., J.F. Bautista, H. Yang, A. Diez-Sampedro, S.A. You, L. Wang, P. Kotagal, H.O. Luders, J. Shi, J. Cui, et al.
2005
. Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Nat. Genet.
37
:
733
–738.
Fettiplace, R., and P.A. Fuchs.
1999
. Mechanisms of hair cell tuning.
Annu. Rev. Physiol.
61
:
809
–834.
Fury, M., S.O. Marx, and A.R. Marks.
2002
. Molecular BKology: the study of splicing and dicing.
Sci. STKE.
2002:PE12.
Ha, T.S., M.S. Heo, and C.S. Park.
2004
. Functional effects of auxiliary β4-subunit on rat large-conductance Ca2+-activated K+ channel.
Biophys. J.
86
:
2871
–2882.
Horrigan, F.T., and R.W. Aldrich.
1999
. Allosteric voltage gating of potassium channels II. Mslo channel gating charge movement in the absence of Ca2+.
J. Gen. Physiol.
114
:
305
–336.
Horrigan, F.T., and R.W. Aldrich.
2002
. Coupling between voltage sensor activation, Ca2+ binding, and channel opening in large conductance (BK) potassium channels.
J. Gen. Physiol.
120
:
267
–305.
Hu, H., L.R. Shao, S. Chavoshy, N. Gu, M. Trieb, R. Behrens, P. Laake, O. Pongs, H.G. Knaus, O.P. Ottersen, and J.F. Storm.
2001
. Presynaptic Ca2+-activated K+ channels in glutamatergic hippocampal terminals and their role in spike repolarization and regulation of transmitter release.
J. Neurosci.
21
:
9585
–9597.
Knot, H.J., N.B. Standen, and M.T. Nelson.
1998
. Ryanodine receptors regulate arterial diameter and wall [Ca2+] in cerebral arteries of rat via Ca2+-dependent K+ channels.
J. Physiol.
508
:
211
–221.
Lippiat, J.D., N.B. Standen, I.D. Harrow, S.C. Phillips, and N.W. Davies.
2003
. Properties of BK(Ca) channels formed by bicistronic expression of hSloα and β1-4 subunits in HEK293 cells.
J. Membr. Biol.
192
:
141
–148.
Meera, P., M. Wallner, and L. Toro.
2000
. A neuronal β subunit (KCNMB4) makes the large conductance, voltage- and Ca2+-activated K+ channel resistant to charybdotoxin and iberiotoxin.
Proc. Natl. Acad. Sci. USA.
97
:
5562
–5567.
Orio, P., and R. Latorre.
2005
. Differential effects of β1 and β2 subunits on BK channel activity.
J. Gen. Physiol.
125
:
395
–411.
Orio, P., P. Rojas, G. Ferreira, and R. Latorre.
2002
. New disguises for an old channel: MaxiK channel β-subunits.
News Physiol. Sci.
17
:
156
–161.
Reinhart, P.H., S. Chung, and I.B. Levitan.
1989
. A family of calcium-dependent potassium channels from rat brain.
Neuron.
2
:
1031
–1041.
Reinhart, P.H., S. Chung, B.L. Martin, D.L. Brautigan, and I.B. Levitan.
1991
. Modulation of calcium-activated potassium channels from rat brain by protein kinase A and phosphatase 2A.
J. Neurosci.
11
:
1627
–1635.
Reinhart, P.H., and I.B. Levitan.
1995
. Kinase and phosphatase activities intimately associated with a reconstituted calcium-dependent potassium channel.
J. Neurosci.
15
:
4572
–4579.
Rothberg, B.S.
2004
. Allosteric modulation of ion channels: the case of maxi-K.
Sci. STKE.
2004:pe16.
Rothberg, B.S., and K.L. Magleby.
1999
. Gating kinetics of single large-conductance Ca2+-activated K+ channels in high Ca2+ suggest a two-tiered allosteric gating mechanism.
J. Gen. Physiol.
114
:
93
–124 (In Process Citation).
Rothberg, B.S., and K.L. Magleby.
2000
. Voltage and Ca2+ activation of single large-conductance Ca2+-activated K+ channels described by a two-tiered allosteric gating mechanism.
J. Gen. Physiol.
116
:
75
–99.
Schubert, R., and M.T. Nelson.
2001
. Protein kinases: tuners of the BKCa channel in smooth muscle.
Trends Pharmacol. Sci.
22
:
505
–512.
Shi, J., G. Krishnamoorthy, Y. Yang, L. Hu, N. Chaturvedi, D. Harilal, J. Qin, and J. Cui.
2002
. Mechanism of magnesium activation of calcium-activated potassium channels.
Nature.
418
:
876
–880.
Stockand, J.D., and S.C. Sansom.
1998
. Glomerular mesangial cells: electrophysiology and regulation of contraction.
Physiol. Rev.
78
:
723
–744.
Weiger, T.M., M.H. Holmqvist, I.B. Levitan, F.T. Clark, S. Sprague, W.J. Huang, P. Ge, C. Wang, D. Lawson, M.E. Jurman, et al.
2000
. A novel nervous system β subunit that downregulates human large conductance calcium-dependent potassium channels.
J. Neurosci.
20
:
3563
–3570.
Xie, J., and D.P. McCobb.
1998
. Control of alternative splicing of potassium channels by stress hormones.
Science.
280
:
443
–446.
Zhang, X., C.R. Solaro, and C.J. Lingle.
2001
. Allosteric regulation of BK channel gating by Ca2+ and Mg2+ through a nonselective, low affinity divalent cation site.
J. Gen. Physiol.
118
:
607
–636.