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Ser165 in the Second Transmembrane Region of the Kir2.1 Channel Determines its Susceptibility to Blockade by Intracellular Mg2+
2 CREST, Japan Science and Technology Corporation, Saitama 332-0012, Japan
Address correspondence to Yoshihiro Kubo, Department of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School and Faculty of Medicine, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan. Fax: (81) 3-5803-5156; E-mail: ykubo.phy2{at}med.tmd.ac.jp
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Key Words: inward rectification • mutation • structure and function • inside-out patch clamp • Kir2.1
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INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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; Vandenberg, 1987; Matsuda, 1988) and polyamines (Ficker et al., 1994; Lopatin et al., 1994; Fakler et al., 1995; Ishihara et al., 1996; Nichols and Lopatin, 1997). Three negatively charged amino acid residues that affect this inward rectification have been identified. The first identified was D172, which is situated in the M2 transmembrane region of Kir2.1 (Fig. 1
A). A D172N Kir 2.1 mutant showed reduced susceptibility to blockade by both cytoplasmic polyamines and Mg2+i (Lu and MacKinnon, 1994; Stanfield et al., 1994; Wible et al., 1994). The second site identified was E224, which is situated in the putative cytoplasmic chain after M2 (Taglialatela et al., 1995; Yang et al., 1995). Finally, we recently identified a third site, E299, which is situated about midway through the putative cytoplasmic chain following the M2 region. This site influences particularly the susceptibility to blockade by spermine (Kubo and Murata, 2001).
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). On the other hand, weak but clear inward rectification remained in the triple Kir2.1 mutant D172N & E224G & E299Q, which also has no negative charges at the indicated sites (Kubo and Murata, 2001). Thus, the difference in the intensities of the inward rectification of currents through Kir2.1 and sWIRK cannot be entirely explained by differences in these three sites. We therefore postulated the presence of one or more additional sites that contribute to the inward rectification.
One aim of the present study was to identify other site(s) that affect the inward rectification of currents through Kir2.1. To accomplish this, we made various mutants based on the comparison of the amino acid sequences of Kir2.1 and sWIRK (Table I)
. We observed that S165L mutation of a D172N & E224G & E299Q triple Kir2.1 mutant markedly weakened inward rectification, and therefore focused on S165, which is located in M2 region (Fig. 1, A and B). In that regard, Thompson et al. (2000) reported that the same S165L mutation of Kir2.1 reduced the susceptibility to blockade by extracellular Rb+ and Cs+ and dramatically increased Rb+ permeance. In that context, our results suggest that the same site affects the susceptibility to blockade by cations from both the intracellular and extracellular sides.
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), whether this finding is applicable to the Kir2.1 inward rectifier is controversial (Minor et al., 1999; Thompson et al., 2000). Therefore, a second aim of this study was to glean useful information about the inward rectification mechanism and about the inner pore structure of Kir 2.1 from data related to the affinities of intracellular and extracellular blockers. |
MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Two-electrode Voltage Clamp Recordings in Xenopus Oocytes
Xenopus oocytes were collected from frogs anesthetized in water containing 0.15% tricaine; after the final collection the frogs were killed by decapitation. Isolated oocytes were treated with collagenase (2 mg/ml, type 1; Sigma-Aldrich) and then injected with 
50 nl of cRNA solution prepared from the linearized plasmid DNA using an RNA transcription kit (Stratagene). The injected oocytes were incubated for 2–4 d at 17°C in frog Ringer solution (Kubo et al., 1993a) supplemented with 20 mM KCl.
Macroscopic currents were recorded in the two-electrode voltage clamp configuration using a bath-clamp amplifier (OC-725C; Warner Co.). Stimulation, data acquisition, and analysis were done on a Pentium-based computer using Digidata 1322A and pCLAMP software (Axon Instruments, Inc.). Intracellular glass microelectrodes were filled with 3 M potassium acetate with 10 mM KCl (pH 7.2). The microelectrode resistances ranged from 0.1 to 0.3 M
. Two Ag-AgCl pellets (Warner Co.) were used to pass the bath current and sense the bath voltage. The voltage-sensing electrode was placed near the oocyte (2 mm away), on the same side as the voltage-recording microelectrode. The bath current–passing pellet and the current injection microelectrode were placed on the other side. Under these conditions, the series resistance between the oocyte surface and the bath voltage-sensing pellet was 200 (Sabirov et al., 1997). As the measured current at the most hyperpolarized potential was 35 µA in the largest case, and was mainly <20 µA, the voltage-clamp error due to this series resistance was estimated to be no more than 7 mV and mostly <4 mV. This error, which was not compensated in the experiments, did not change the conclusions drawn from the comparison of wild-type and mutant channels.
All recordings in this work were performed at room temperature (20–23°C). For the data summarized in Figs. 2–4 and 9 A, the recording bath solution contained 10 mM KCl, 80 mM N-methyl-glucamine, 70 mM HCl, 3 mM MgCl2, and 10 mM HEPES, pH 7.4. For the data on Rb+ permeance in Fig. 9 B, the recording bath solution contained 10 mM RbCl, 80 mM N-methyl-glucamine, 70 mM HCl, 3 mM MgCl2, and 10 mM HEPES, pH 7.4. By assuming an intracellular potassium concentration ([K+]i) of 80 mM, the EK was calculated to be -52 mV; however, the exact values of [K+]i and EK for each oocyte are unknown. The EK used for the calculation of the chord conductance (Figs. 2 and 3) was therefore adjusted to yield a continuous G-V plot. The adjusted EK ranged from -54 to -49 mV.
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Data from the same batch of oocytes were used for comparison of phenotypes (Figs. 2–4 and 9) because properties such as inward rectification and blocking speed, which are influenced by the cytoplasmic polyamine concentration, differ significantly from batch to batch. Nevertheless, similar tendencies were reproducibly observed in five batches of oocytes.
Single-channel Recordings in Xenopus Oocytes
For single-channel recording, the vitelline membrane was peeled off by bathing the oocytes for 5–10 min in a hyperosmolar solution (Kubo et al., 1993a). The patch pipettes were prepared from borosilicate glass (Warner Instruments) using a P-97 horizontal puller (Sutter) and a fire polisher (Narishige). Pipette resistance ranged from 4 to 9 M. Recordings were obtained under the cell-attached configuration using an AxoPatch 1D amplifier (Axon Instruments, Inc.). The recorded currents were low pass filtered at 1 kHz using a Bessel filter built into the amplifier and digitized at 5 kHz. The recordings shown in Fig. 12 A were digitally filtered at 500 Hz. The pipette (extracellular) and bath solutions contained 136 mM KCl, 3 mM MgCl2, 10 mM HEPES, and 4 mM KOH, pH 7.4.
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). The plasmid DNA was then cotransfected into HEK293T cells (human embryonic kidney cell line) along with a transfection marker, enhanced green fluorescent protein (GFP) (CLONTECH Laboratories, Inc.; 1/15 the amount of plasmid DNA), using Lipofectamine Plus (GIBCO BRL) as instructed by the manufacturer. The cells were cultured in Dulbecco's modified Eagle's medium with 10% bovine calf serum for 24 h. The transfectants were then dissociated by treatment with 0.025% trypsin in Ca2+- and Mg2+-free PBS, and reseeded on coverslips at a relatively low density. The reseeding was done to obtain well-isolated cells and to facilitate successful giga-ohm seal formation. Prior to experimentation, we confirmed that the trypsin treatment did not change the electrophysiological properties of the expressed channels. Electrophysiological recordings were performed 7–24 h after reseeding, which corresponds to 18–35 h after transfection.
Macroscopic Current Recordings in HEK293T Cells
A coverslip with HEK293T cells was placed in a recording chamber containing bath solution (see below) on the stage of an inverted fluorescence microscope (IX70; Olympus), and the transfected cells were identified by the fluorescent signal of the cotransfected GFP. Macroscopic currents were then recorded in the excised inside-out patch configuration using an Axopatch-1D amplifier. The resistance of the patch pipettes ranged from 2 to 4 M. 50–80% of the voltage error due to the series resistance was compensated by a circuit in the amplifier. The level of expression achieved with the combination of HEK293T cells and the pCXN2 expression was sufficient for macroscopic current recording using standard-sized patch pipettes. The recorded currents were low-pass filtered at 1 kHz by a circuit built into the amplifier.
The pipette (extracellular side) solution contained 16 mM KCl, 120 mM NMG, 102 mM HCl, 3 mM MgCl2, 10 mM HEPES, and 4 mM KOH, pH 7.4 (Figs. 5–8 and 10 A), or 16.6 mM RbCl, 120 mM NMG, 102 mM HCl, 3 mM MgCl2, 10 mM HEPES and 3.4 mM RbOH (pH 7.4) (Fig. 10 B). The bath (intracellular side) solution containing various concentrations of Mg2+ or spermine was prepared as described by Ishihara et al. (Ishihara et al., 1996) with some modifications. We used KH2PO4 and K2HPO4 as a pH buffer because HEPES, or some accompanying impurity, reportedly causes inward rectification (Guo and Lu, 2000). Mg2+- and spermine-free solution contained 116.88 mM KCl, 2 mM EDTA, 2.83 mM KH2PO4, 7.17 mM K2HPO4, and 5.95 mM KOH (pH 7.2). MgCl2 was added to adjust the free Mg2+ concentration; the amount added was calculated using the free software Sliders v2.00 (Chris Patton, Stanford University, http://www.stanford.edu/~cpatton/maxc.html). The amounts of added MgCl2 and the (free Mg2+) concentration were: 1.06 mM (3.00 µM), 1.87 mM (30.5 µM), 2.28 mM (298 µM), and 5 mM (3 mM). The acidic shift in pH caused by adding MgCl2 was adjusted to pH 7.2 by applying KOH, and the total K+ concentration was adjusted to 140 mM. Spermine (Sigma-Aldrich) was simply added to the solution just before the experiments, and solutions containing spermine were used for up to 2 h. The concentration of added spermine is indicated in Figs. 7–8. The total [K+]o and [K+]i were 20 and 140 mM. The liquid junction potential between the pipette solution and the bath solution was 11 mV (Figs. 5–8 and 10 A) or 8 mV (Fig. 10 B); membrane potentials were corrected for this value.
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Cysteine-scanning Mutagenesis
The accessibility of cys-modifying reagents from extracellular side was analyzed as we described previously (Kubo et al., 1998) using Xenopus oocytes under two-electrode voltage clamp. The bath solution contained 24 mM KCl, 66 mM N-methyl-glucamine, 42 mM HCl, 3 mM MgCl2, and 5 mM HEPES pH 7.4 (Fig. 13 A). By assuming an intracellular potassium concentration ([K+]i) of 80 mM, the EK was calculated to be -30 mV. The accessibility from intracellular side was analyzed as described by Lu et al. (1999) using transfected HEK293 cells by inside-out patch clamp macroscopic current recording. The pipette (extracellular) and the bath (intracellular) solution with no Mg2+ and spermine was the same as those used in Figs. 5–8. Cys-modifying reagents, 2-trimethylammonium ethyl methane-thiosulfonate bromide (MTSET; Toronto Research) and 2-aminoethyl methane-thiosulfonate bromide (MTSEA; Toronto Research) were dissolved in the bath solution just before use, and one-fifth volume of five times the concentrated stock solution of them or Cd2+ was applied to the bath and was mixed immediately through pipetting.
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RESULTS |
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Initially, the electrophysiological effects of S165L mutation on wild-type Kir2.1 and its D172N and D172N & E224G & E299Q triple mutants were compared (Fig. 2) . Macroscopic currents recorded in 10 mM K+ using two-electrode voltage clamp in Xenopus oocytes are shown in Fig. 2 A; also shown are the I-V (Fig. 2 B) and G-V (Fig. 2 C) relationships. As an index of the intensity of the inward rectification, the ratios of the current amplitudes at 50 and -100 mV were calculated (Fig. 4 A).
S165L mutation did not affect the inward rectification of currents through the wild-type channel remarkably. The I-V relationship for the D172N mutant showed a notable outward hump, and rectification was weaker than in the wild-type channel. Introduction of the S165L mutation into the D172N mutant did not substantially alter these findings. The D172N & E224G & E299S triple mutant showed a large outward current and significantly weakened rectification. Moreover, addition of the S165L mutation decreased the inward rectification still further, so that large outward currents were observed even at the most depolarized potentials (Fig. 2 A). These results suggest that S165 is a key determinant of the strength of the inward rectification of currents through Kir2.1, but its significance is masked in the presence of E224 and E299, which mediate strong rectification.
It was also notable that the S165L mutation affected the G-V relationship at hyperpolarized potentials (Fig. 2 C). The conductance of wild-type Kir2.1 saturated at potentials more hyperpolarized than -100 mV, and that of the D172N mutant showed a slight decrease in the peak conductance. Upon introduction of the S165L mutation, however, neither the wild-type channel nor the D172N mutant reached saturation even at the most hyperpolarized potential recorded (-160 mV) (Fig. 2 C). The same effect was observed in the triple mutant and suggests that the S165L mutation may also affect the permeation properties of the channel.
The Effect of the Amino Acid Residue at Position 165 on Inward Rectification
We next substituted selected amino acids for S165 in the D172N & E224G & E299S triple mutant and analyzed the electrophysiological properties using two-electrode voltage clamp (Fig. 3)
. The inward rectification properties of the various mutants were classified into two groups: one group with G, I, or L at position 165 showed very weak inward rectification, whereas the other group with E, D, T, or S at position 165 showed relatively strong inward rectification (Figs. 3 and 4
B). In the latter group, the amino acid residue at 165 is hydrophilic and has a COOH- (E, D) or OH- group (T, S) in the side chain. This implies that, as in the cases of D172 (Lu and MacKinnon, 1994) and E224 (Yang et al., 1995) mutants, the electrostatically negative environment of the OH- group of Ser165 contributes to inward rectification, and that the phenotype of the S165L mutant is not due to the L itself. Still, slight differences were observed even between mutants in the same group (e.g., L and G, D and E) (Fig. 4 B), perhaps due to differences in the size, shape, and chemical properties of the amino acid residue at position165. To further examine the effect of electrostatic charge at this residue, we made an S165K mutant, but it did not allow any detectable current. The analysis summarized below was performed using S165L as a representative mutation.
Comparison of the Susceptibility of Wild-type and Mutant Kir2.1 to Blockade by Spermine
Since inward rectification is caused by blockage of the channel by cytoplasmic Mg2+ or polyamines, we next determined how the susceptibility to blockade by these inhibitors was affected by S165L mutation. Macroscopic currents were recorded in the presence of spermine from inside-out membrane patches excised from HEK293T cells expressing wild-type or mutant Kir2.1 (Fig. 5) . In the cases shown, prominent outward currents were observed when no spermine was present, indicating that endogenous cytoplasmic polyamines had been washed out. In the case of the D172N mutant, a weak but significant rectification remained consistently, even after intensive exchange of the intracellular solution (Fig. 5–8). We speculate that cytoplasmic blockers tend to remain in D172, but the details are unknown.
The I-V relationships were determined from a set of measurements obtained 3 s after the onset of each step pulse. Because the run-down phenomenon made it very difficult to obtain a full dataset in which the inward current amplitude remained stable throughout, we compared the I-V relationships and rectification using data from multiple patches by normalizing the current amplitude to the values at -90 mV (-40 mV from EK) (Fig. 6 A). In addition, because blockage by spermine showed a strong voltage dependency, especially in the D172N and D172N & S165L mutants, rectification indexes at two voltages, -10 mV (40 mV from EK) and 30 mV (80 mV from EK) were calculated. An index of 2 was set as 100% at 30 mV because the driving force at that voltage was twice that at -90 mV when EK is -50 mV; an index of 1 was set as 100% at -10 mV because the driving force at that voltage was the same as at -90 mV. The means ± SD (n = 3–7) of the fractions were then plotted against spermine concentration (Fig. 6 B). The fractions at -10 and 30 mV in e.g., 1 µM spermine did not change by introducing S165L mutation significantly (P > 0.05, Student's unpaired t test) on the backgrounds of wild-type, D172N and the triple mutant.
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The wild-type Kir 2.1 channel was highly sensitive to spermine; D172N was less so, and D172N & E224G & E299S was even less sensitive than D172N. As indicated by the overlap of the fitted curves depicted by the solid (Ser165) and dotted (S165L mutation) lines in Fig. 6 B, S165L mutation did not clearly affect the susceptibility to spermine blockade. Apparently, D172, E224, and E299 are critical for Kir2.1 sensitivity to spermine, but S165 is not. This confirms the assumption that spermine plugs the pore at the level of D172 and suggests that S165, which is situated at a narrow site farther from the intracellular side of the membrane than D172, is not accessible to bulky cytoplasmic spermine.
Comparison of the Susceptibility of Wild-type and Mutant Kir2.1 to Blockade by Mg2+i
Addition of free Mg2+i (calculated as described in MATERIALS AND METHODS) blocked the outward current through the wild-type Kir2.1 at depolarized potentials almost instantaneously, but the effect developed much more slowly in the S165L mutant (Fig. 7) . This slow blockade of outward currents was characteristic of S165L mutation, and was also observed in the D172N & S165L double mutant and in the triple & S165L mutant. In addition, it was clear from the normalized I-V relationship to the value at -90 mV (-40 mV from EK) that the strength of the rectification at each Mg2+i concentration—i.e., the susceptibility to blockade by Mg2+i—was reduced by the introduction of the S165L mutation in all cases (Fig. 8
A). Mg2+i concentration-block relationships were determined by normalizing the current amplitude at 30 mV (
) and -10 mV (
) to the values at -90 mV. In most cases, rectification indexes of 2 and 1 were set as 100% at 30 and -10 mV, respectively. For the data from the D172N and triple & S165L mutants, indexes of 2.25 and 1.75 were set as 100% at 30 mV. These adjustments were done to practically optimize the curve fitting and we speculate that they reflect changes in the rectification properties in the absence of cytoplasmic blockers of these two channels. The fractions at -10 and 30 mV in, for example, 3,000 µM Mg2+ changed by introducing S165L mutation significantly (P < 0.01, Student's unpaired t test) on the backgrounds of wild-type, D172N, and triple mutant.
The plotted mean values were then fitted with Hill's equation (Fig. 8 B). The Ki and Hill coefficient values at -10 mV were: 410 µM and 0.35 (wild-type), 1310 µM and 0.17 (S165L), 740 µM and 0.77 (D172N), 23000 µM and 0.28 (D172N & S165L), 830 µM and 0.39 (triple mutant), 9.9 x 108 µM and 0.11 (triple mutant & S165L). The values at 30 mV were: 120 µM and 0.30 (wild-type), 210 µM and 0.18 (S165L), 190 µM and 0.47 (D172N), 6,100 µM and 0.28 (D172N & S165L), 210 µM and 0.38 (triple mutant), 2.5 x 106 µM and 0.13 (triple mutant & S165L).
These results suggest that either S165 or D172 alone could account for the channel's sensitivity to Mg2+i and that mutations of both sites dramatically diminished sensitivity. Together, these findings indicate that both D172 and S165 play a crucial role in determining the susceptibility of Kir2.1 to blockade by Mg2+i. We therefore conclude that S165 is a novel residue crucially involved in Mg2+i blockade.
Effect of S165L Mutation on Rb+ Permeation of Kir 2.1
Macroscopic currents in 10 mM K+ (Fig. 9
A) and 10 mM Rb+ (Fig. 9 B) were recorded from the same oocytes using two-electrode voltage clamp; the I-V relationships are plotted in Fig. 9 C. Rb+ permeance indexes (Thompson et al., 2000), calculated as IRb+(-120 mV)/IK+(-120 mV), are shown in Fig. 11 A. Wild-type Kir 2.1 showed a very low Rb+ permeance, and S165L mutation increased it dramatically. D172N mutation caused only a slight increase. In the background of D172N and the triple mutant, S165L mutation again increased Rb+ permeance dramatically (Fig. 11 A).
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reported that the surface charge screening component by polyamine affects the apparent reversal potential by shifting it toward negative direction from the real value. The very small amplitude of outward current in the presence of polyamine also makes the determination of reversal potentials inaccurate. For these two reasons, we measured the reversal potentials by inside-out patch clamp recording in the absence of intracellular Mg2+i and spermine. Macroscopic currents were recorded by applying ramp pulses of 800 ms from -150 to 50 mV, in 20 mM [Ko+]/140 mM [Ki+] (Fig. 10
A) and 20 mM [Rbo+]/140 mM [Ki+] (Fig. 10 B). Erev(K+o) and Erev(Rb+o) of wild-type Kir2.1 were -49.8 ± 1.80 mV and -69.6 ± 4.0 mV (Fig. 11
B). In comparison with the wild-type, Erev(Rb+o) were shifted to depolarized potentials while Erev (K+o) did not change in the S165L, D172N, and D172N & S165L mutants. The values were -48.9 ± 1.6 mV (Erev(K+o)) and -61.7 ± 3.4 mV (Erev(Rb+o)) in the S165L mutant, -48.4 ± 1.7 mV (Erev(K+o)) and -61.3 ± 2.5 mV (Erev(K+o)) in the D172N mutant, -50.0 ±1.6 mV (Erev(K+o)) and -60.3 ± 1.5 mV (Erev(Rb+o)) in the D172N & S165L mutant (Fig. 11 B). The permeability ratios of Rb+ and K+ (PRb+/PK+), calculated from the shift of the reversal potential by the Nernst equation, were 0.46 (wt), 0.60 (S165L), 0.60 (D172N), and 0.66 (D172N & S165L), showing that both S165L and D172N mutation equally increased permeability of Rb+ relative to K+. Together, S165 and D172, which determine the susceptibility to intracellular blockers, were shown to be crucial determinants of Rb+ permeability. That D172N mutation caused only a slight increase in Rb+ permeance, but S165L mutation dramatically increased it is indicative of the difference in the functions D172 and S165 for Rb+ permeation.
Comparison of the Single-channel Conductances through Wild-type and Mutant Kir2.1
Single-channel recordings were obtained from Xenopus oocytes using the cell-attached patch configuration in 140 mM K+o. Recordings at -80, -120, and -160 mV are shown in Fig. 12
, although in the case of the D172N & S165L double mutant, data were recorded at -120, -160, and -200 mV because the single channel current amplitudes were very small. The I-V relationships and the accumulated data on the single-channel conductance shown in Fig. 12, B and C, respectively, suggest that S165 contributes to the permeation properties in cooperation with D172.
Accessibility of the S165C Residue by Cys-modifying Reagents Applied from either the Intracellular or Extracellular Side
To gain insight of the structure of S165 and surrounding regions of Kir2.1, we next analyzed the accessibility of S165C residue by Cys-reacting reagents from either extracellular (Fig. 13, A and C) or intracellular (Fig. 13, B and D) side.
The accessibility from the extracellular side was examined as we described previously (Kubo et al., 1998). As endogenous Cys149 of the wild-type Kir2.1 gives a background modification, we first introduced C149F mutation, and used it as a negative control. We then introduced F147C mutation at the external entrance of the pore on the background of C149F, and used this C149F & F147C mutant as a positive control of modification. S165L mutation was introduced also on the background of C149F (C149F & S165L). Application of MTSET (100 µM), MTSEA (100 µM), or Cd2+ (100 µM) decreased the current of C149F & F147C, but not of C149F or of C149F & S165C, showing the lack of accessibility of S165C by these reagents from extracellular side (Fig. 13, A and C). As we observed that T141C is accessible from extracellular side (Kubo et al., 1998), S165 was shown to locate at a deeper position from extracellular side than T141.
Lu et al. (1999) reported a systematic analysis of the accessibility of various amino acid residues of Kir2.1 from intracellular side. They first made a construct named IRK1J as a negative control in which endogenous Cys residues causative of modification from inside were mutated. They showed that S165C could not be modified from intracellular side by MTSET or MTSEA. To confirm their observation, we performed a similar analysis using IRK1J as a negative control and IRK1J & S165C. We observed that neither MTSET (2 mM) nor MTSEA (2.5 mM) caused clear modification of IRK1J & S165L at a level apparently different from that observed in IRK1J (Fig. 13, B and D), suggesting that S165C was not accessible from intracellular side by these reagents. We also tried to analyze the effect of Cd2+, but failed to draw a reliable conclusion, due to a severe reversible block of current which hindered an accurate estimation of the extent of Cys modification.
Significance of the Corresponding Amino Acid Residue to Ser 165 in other Kir Family Members
To examine whether the amino acid residue corresponding to S165 of Kir 2.1 is important for inward rectification of currents through other Kir family members, we substituted S164 in Kir 1.1 and L169 in sWIRK. The Kir1.1 S164L mutant did not allow any detectable current. In the case of sWIRK, we substituted L169 with S, T, Y, E, D, Q, N, C, G, A, V, I, or K, but only the L169I mutant allowed detectable current that was very similar to that of the wild-type sWIRK (unpublished data).
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DISCUSSION |
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Functional Roles of the Four Residues that Define the Inward Rectification Properties of Kir2.1
The scheme shown in Fig. 14
depicts the four amino acid residues identified to be critical for inward rectification of currents through Kir2.1 (D172, E224, E299, and S165).
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; Stanfield et al., 1994; Wible et al., 1994). It was later shown to also be critical for the susceptibility to blockade by polyamines (Yang et al., 1995). It has been speculated that spermine plugs the pore at D172 (Lopatin et al., 1995; Pearson and Nichols, 1998) and that partial blockade by Mg2+i occurs at this site (Oishi et al., 1998).
(b and c) E224 and E299. E224, which was originally thought to be situated in the cytoplasmic region after M2 (Kubo et al., 1993a), was shown in 1995 to contribute to the susceptibility to the blockade by polyamines and to form part of the permeation pathway (Yang et al., 1995). In addition, it was reported recently that E299, which was originally thought to be near the midpoint of the long-cytoplasmic chain after M2 (Kubo et al., 1993a) also contributes to inward rectification and, like E224, forms part of the inner pore (Kubo and Murata, 2001; Xie et al., 2002). In that study, we considered the likelihood that E224 and E299 are located at the inner vestibule and serve as intermediate binding (nonplugging) sites that facilitate entry and exit of spermine to and from the final pore-plugging binding site located deeper in the pore (Kubo and Murata, 2001). It was postulated that E224 and E299 serve to increase the local concentration of spermine at the inner vestibule (Kubo and Murata, 2001; Xie et al., 2002).
(d) S165. In the present work, we identified S165 as the fourth site that contributes to the inward rectification of currents through Kir 2.1. S165L mutation affected the susceptibility to blockade by Mg2+i, but not by spermine (Figs. 2–8).
Structure of the Kir 2.1 Inner Pore with Respect to the Susceptibility to Intracellular Blockers
The high-resolution structure of the bacterial KcsA channel was resolved by X-ray crystallography (Doyle et al., 1998) and might be applicable to the structure of all K+ channels. If this is the case, S165 of Kir 2.1 corresponding to M96 of KcsA would be predicted to form an intersubunit hydrogen bond and not to face to the aqueous pore. Our observation that S165C was not modified by Cys-reacting regents (Fig. 13) could be explained by this structure. Also, as S165L mutation might produce severe changes in the overall structure of the pore by destroying the hydrogen bonds, the significant change in Rb+ permeance we observed could be explained by this assumption (Figs. 9–11). However, by making several different substitutions at S165 on the background of the D172N & E224G & E299Q mutant, we observed that functional channel property was maintained, and that the negatively charged atmosphere of the side chain determines the inward rectification property (Figs. 3 and 4). These results imply that S165 faces to the aqueous pore rather than that it forms an intersubunit hydrogen bond.
Based on random mutagenesis and a yeast genetic screening method, Minor et al. (1999) concluded that the structural correspondence between Kir 2.1 and KcsA is not necessarily high. Their identification of the pore-lining and M1/M2 intersubunit interface residues of Kir2.1 indicated that the M2 region of Kir 2.1 forms an 
-helix and S165, C169, D172, and I176 are not part of an intersubunit interface, but are surface residues mediating protein–water interaction (Minor et al., 1999). This proposal is consistent with our observation that various mutations at S165 determine the susceptibility to blockade by Mg2+i.
By combining cysteine scanning mutagenesis and covalent chemical modification, Lu et al. (1999) determined that the inner vestibule of Kir 2.1 at the level of D172 is spacious enough to fit multiple methane-thio-sulfonate reagents (e.g., MTSET and MTSEA). They also reported that these reagents did not modify S165. We repeated this experiment using MESET and MESEA and confirmed that S165C is not covalently modified. We interpret these data to imply most likely that the inner pore at the level of S165 is too narrow for methane-thio-sulfonate reagents to access, although S165 faces to the aqueous pore. Our finding that the S165L mutant did not change the susceptibility to spermine blockade, but decreased the susceptibility to Mg2+i blockade, goes very well with this interpretation. Minor et al. (1999) reported that S165 is situated two -helix turns up from D172. In that context, our findings suggest that the inner vestibule of Kir2.1 is relatively wide at the level of D172, but has narrowed at the level of S165; consequently, Mg2+i but not spermine can access S165 (Fig. 14).
As mutants of other Kir family members at the corresponding amino acid to S165, S164L of Kir1.1 and L169S of sWIRK, did not allow any detectable current, it is likely that the structures of Kir1.1, sWIRK and Kir 2.1 differ significantly—e.g., Kir 1.1 S164 and sWIRK L169 might participate in inter-subunit hydrogen bonding, as is known for KcsA.
S165 Is the Key Residue Accessed by Both Extracellular and Intracellular Blockers
Thompson et al. (2000) reported that the S165L mutant showed large inward Rb+ currents at negative voltages below the reversal potential, although inward currents through wild-type Kir 2.1 were blocked by extracellular Rb+; that Rb+ permeance was increased further in the S165L & T141A double mutant, and even further in the S165L & T141A & D172N triple mutant; that both S165L and T141A mutation significantly reduced Cs+ blockade; that the S165L and T141A double mutant were nearly insensitive to Cs+; and that D172N mutation did not alter Cs+ sensitivity. Since S165 is situated farther from the extracellular side than the GYG K+ selectivity filter (Heginbotham et al., 1992; Doyle et al., 1998; Minor et al., 1999), they speculated that extracellular blocking cations, such as Rb+ and Cs+, must traverse the GYG selectivity filter in Kir 2.1.
In the present study we analyzed the effect of S165L mutation on Rb+ permeance and PRb+/PK+ in wild-type Kir 2.1 and the D172N mutant. Rb+ permeability was increased by D172N and S165L mutation, and inward Rb+ currents were dramatically increased by S165L mutation, but only slightly by D172N mutation. This suggests that both S165 and D172 play a role in Rb+ permeation and selectivity (Fig. 14), and their functions differ.
T141 is known to be easily accessible to several cations from the extracellular side. For instance, we used a cysteine scan mutagenesis analysis of a T141C mutant to show that Cd2+ could access the site from the extracellular side (Kubo et al., 1998). In addition, Dart et al. (1998) reported accessibility of Ag+ to this site, and Alagem et al. (2001) showed that T141 is involved in the stabilization of Ba2+ binding. When we examined the accessibility of S165C to Cd2+ from extracellular side, we observed no modification. S165 is thus apparently located at a position farther from extracellular side than T141, at a point where the pore is narrower and accessible to Rb+ and Cs+, but not to Cd2+ (Fig. 14). We therefore propose that Ser165 forms the narrowest part of the pore, the point at which both extracellular and intracellular blockers plug the permeation pathway. This makes S165 a key determinant of ion permeability, selectivity and rectification.
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FOOTNOTES |
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ACKNOWLEDGMENTS |
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This work was supported partly by the research grants from the Ministry of Education, Science, Sports, Culture, and Technology of Japan and from foundations of Umami, Kowa, Novartis, and Salt Science.
Submitted: 9 July 2002
Revised: 25 September 2002
Accepted: 26 September 2002
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).
), and D172N & S165L (+) channels. (C) Single-channel conductance calculated from the slopes of the plots in B; plotted are means ± SD (n = 4–6).
), 1 µM (
), triple mutant (
