Functional roles of the amino terminal domain in determining biophysical properties of Cx50 gap junction channels

Abstract

Communication through gap junction channels is essential for synchronized and coordinated cellular activities. The gap junction channel pore size, its switch control for opening/closing, and the modulations by chemicals can be different depending on the connexin subtypes that compose the channel. Recent structural and functional studies provide compelling evidence that the amino terminal (NT) domains of several connexins line the pore of gap junction channels and play an important role in single channel conductance (γ_j) and transjunctional voltage-dependent gating (V_j-gating). This article reviews recent studies conducted on a series of mutations/chimeras in the NT domain of connexin50 (Cx50). Functional examination of the gap junction channels formed by these mutants/chimeras shows the net charge number at the NT domain to be an important factor in γ_j and in V_j-gating. Furthermore, with an increase in the net negative charge at the NT domain, we observed an increase in the γ_j as well as changes in the parameters of the Boltzmann fit of the normalized steady-state conductance and V_j relationship. Our data are consistent with a structural model where the NT domain of Cx50 lines the gap junction pore and plays an important role in sensing V_j and in the subsequent conformational changes leading to gating, as well as in limiting the rate of ion permeation.

Introduction

Gap junction channels provide a direct passage for ions and small signaling/metabolic molecules to be exchanged between neighboring cells. Each gap junction channel is formed by two hemichannels docked end-to-end at the extracellular domains. Each hemichannel is an oligomer of six connexins (Cxs). Connexins are a group of homologous proteins encoded from 21 genes in the human genome (20 genes in the rodent genome) (Sohl and Willecke, 2004). Each connexin has its own unique tissue distribution and each tissue cell often expresses one or more connexins (Simon and Goodenough, 1998; Laird, 2006).

Gap junction channels can be gated via a variety of factors, including pH changes, intracellular calcium concentrations and transjunctional voltage (V_j) (Verselis et al., 1994; Bukauskas and Peracchia, 1997; Peracchia et al., 2000; Bukauskas and Verselis, 2004; Gonzalez et al., 2007). V_j is the voltage difference between the interiors of two gap junction linked cells. V_j-dependent closure of the gap junction channel, known as V_j-gating, is a common property for all characterized gap junction channels. However, the extent and sensitivity of V_j-gating of different gap junction channels can vary drastically (Burt and Spray, 1988; Barrio et al., 1991; Verselis et al., 1994; Purnick et al., 2000). Earlier studies on Cx26, Cx32 and other connexins have indicated that among several domains, the NT domain and the residue within the NT domain play a crucial role in gating polarity, the properties of V_j-gating and unitary conductance (Rubin et al., 1992; Verselis et al., 1994; Purnick et al., 2000; Musa et al., 2004; Peracchia and Peracchia, 2005; Srinivas et al., 2005; Dong et al., 2006; Gemel et al., 2006; Verselis and Srinivas, 2008; Kronengold et al., 2012). The molecular basis of V_j-gating is not fully understood. Here we summarize some recent experimental evidence which shows that V_j-gating properties and unitary conductance of Cx50 gap junction channels depend on the NT domain, especially, the charged residues. We also discuss our findings relating to the atomic structure of gap junction channels to examine the structure-function relationship of gap junction channels at the submolecular domains and individual amino acid residues.

Structural models of gap junction channels

Gap junction channels are formed by the oligomerization of connexin molecules. Hydropathy analysis of connexin protein sequence predicts that each connexin has four transmembrane domains (M1–4), two extracellular domains (E1 and E2), one intracellular loop (IL), and the carboxyl terminus (CT) and the amino terminus (NT) in the cytosol (Nicholson, 2003; Saez et al., 2003). Based on various experimental approaches, several different gap junction channel structural models have been proposed and each provides some unique insights into the structure of the gap junction channel (Foote et al., 1998; Perkins et al., 1998; Unger et al., 1999; Muller et al., 2002; Nicholson, 2003). However, due to limited spatial resolution, the atomic structure of gap junction channels has not been resolved until recently. Maeda, Tsukihara and colleagues crystallized the Cx26 gap junction channel and provided the first atomic structure model at 3.5 Å resolution for this channel (Maeda et al., 2009; Suga et al., 2009). This high resolution structural model confirmed many structural features previously predicted. For example, the four transmembrane domains in each connexin form α-helical structures and the extracellular domains appear critical for the docking interactions (Maeda et al., 2009; Nakagawa et al., 2011; Gong et al., 2013). More importantly, the high resolution model provided greater detail and also revealed several novel structural features. One interesting, and somewhat surprising, feature of the Cx26 channel structure was that the NT domain of each connexin molecule folded into the gap junction pore and contributed to the lining of a portion of the pore inner surface (Figure 1A). In addition, six NT domains of Cx26 formed a funnel structure at the pore entrances and the funnels were the narrowest parts of the channel (Maeda et al., 2009; Maeda and Tsukihara, 2011). This kind of spatial arrangement provides a structural advantage for the NT domain in sensing a voltage change across the channel, which makes the NT domain a good determinant of V_j-gating. The small physical channel pore diameter and the surface electrical charges at the site of NT domains form physical and electrical barriers to ions going through the channel, respectively. Therefore, the NT domain may also be important in limiting the rate of ion permeation through a channel, a parameter that can be quantitatively measured as the single (or unitary) channel conductance (γ_j).

Figure 1

The NT domains, together with the transmembrane domains (M1–4), and extracellular loops (E1 and E2) of different connexins, are highly conserved among all connexins. We aligned the mouse Cx50 and Cx36 sequences with that of the human Cx26 using Jalview (Waterhouse et al., 2009). The results indicated that both Cx50 (56.4% sequence identity) and Cx36 (48.2% sequence identity) are highly similar to that of the Cx26 (Waterhouse et al., 2009). At this high level of conservation, it is reasonable to speculate that Cx50 and Cx36 may take a similar structure as Cx26 channels. We hypothesized that the NT domains for Cx50 and Cx36 line the respective gap junction channel pore and play an important role in their V_j-gating and γ_j. Topology structural models of Cx50 and Cx36 are shown in Figure 1B. We aligned the protein sequence of the beginning portion of the NT domains of Cx50 and Cx36 and labeled all the charged residues (Figure 1) (Xin et al., 2012a). It was very interesting to note that there are 5 charged residues in the NT of Cx36 (3 negative and 2 positive), and 5 charged residues in the NT of Cx50 (4 negative and 1 positive). A simple mathematical summation of all the charges gave the net charge of the Cx36 NT domain, −1, and that of the Cx50 NT domain, −3. Considering hexameric oligomerization of connexins to form one hemichannel, the net charge of the NT domains of the Cx36 hemichannel was −6 and that of Cx50 hemichannel was –18. End-to-end mirror symmetrical docking of two hemichannels was required to form a whole gap junction channel, which had twice the net charges of the NT domains. Thus, in theory, a minor change in the NT domain net charge is amplified 6 times in the hemichannel and 12 times in the whole gap junction channel. To test how the change in the NT net charge affects the channel V_j-gating and γ_j properties, we systematically compared results across a number of mutants/chimera of Cx50.

Functional studies using chimera and mutagenesis approaches

The technical approach we adopted was to heterologously express the mutant and wild-type connexins in gap junction deficient neuroblastoma (N2A) cells. Co-expression of the green fluorescent protein (GFP) was used to increase the success rate of identifying cell pairs expressing the mutant construct. We generated a series of mutants and chimeras, in which a single amino acid residue, or a short segment of amino acid residues between the two NT domains of the selected connexins, was exchanged. Using a double patch-clamp whole-cell recording method, we quantitatively measured V_j-gating and γ_j of channels formed by these mutants/chimeras (Xin et al., 2010, 2012a,b). It was fortunate that many of these mutants/chimeras at the NT domain of Cx50 resulted in the formation of homotypic gap junction channels, with readily identifiable V_j-gating characteristics and measurable γ_js. The generated chimera included Cx50Cx36N, in which the NT domain of Cx50 was replaced by that of the Cx36 (Figure 1C). Other mutants, Cx50N9R, Cx50GNI (a triple mutation composed of G8E, N9R and I10L), and Cx50G8E, were also generated with site-directed mutagenesis, using wild-type Cx50 as a template (Figure 1C).

We ranked the mutants, chimera and wild-type connexins according to the NT net charges in Figure 1C. The net charges range from −1 (Cx36 and Cx50Cx36N), −2 (Cx50N9R), −3 (Cx50GNI and Cx50) to −4 (Cx50G8E) in these mutants/chimera and wild-type connexins.

v_j-gating of Cx50, Cx36, and Cx50 mutants/chimera

Cx50 is expressed primarily in the lens and serves an important function in keeping the lens transparent (Saez et al., 2003). Knockout of the Cx50 gene in mouse leads to nuclear cataracts and microphthalmia (White et al., 1998). Cx36 is expressed in neurons and plays a role in synchronized neuronal activities (Perez Velazquez and Carlen, 2000). Mice lacking the Cx36 gene have disrupted or significantly reduced electrical coupling between interneurons in the neocortex and hippocampus, and reduced γ-frequency (30–70 Hz) rhythms in the hippocampus (Hormuzdi et al., 2001; Buhl et al., 2003). It is very hard to characterize gap junction channel properties in neurons due to one or more of the following reasons: extended arborization and complexity of neuronal dendritic trees, the existence of many active ion channels on the plasma membrane, and the remote location of gap junction channels from the recording sites (Connors and Long, 2004). The channel biophysical properties are mostly characterized from studies using recombinant expression of Cx36 or Cx50 in gap junction deficient cell lines (Srinivas et al., 1999b; Al-Ubaidi et al., 2000).

Homomeric homotypic gap junction channels formed by the Cx36 appear to be drastically different from the Cx50 channels in their V_j-gating properties and single channel conductance (γ_j). The gap junction channels formed by Cx36 possess one of the lowest single channel conductance (γ_j = 4–15 pS) among many characterized gap junction channels (30–300 pS) (Srinivas et al., 1999b; Teubner et al., 2000; Moreno et al., 2005). In addition, V_j-gating of Cx36 gap junction channels are the weakest among all gap junction channels (more details are provided below). Cx50 gap junction channels, on the other hand, show large single channel conductance ~200 pS and pronounced V_j-gating (Srinivas et al., 1999a; Bai et al., 2006; Xin et al., 2010). Little information is available as to which domains and amino acid residues of Cx36 or Cx50 are critical for their unique channel properties. We hypothesize that the V_j-gating and single channel conductance (γ_j) properties of the Cx36 or Cx50 gap junction channels are encoded in part by the NT domain.

To investigate the role of the NT domain we generated a chimera (Cx50-Cx36N) in which the NT domain of the Cx36 was switched into Cx50. The V_j-gating properties of Cx50-Cx36N displayed some novel properties and also adopted some features from their “parental” connexins. As shown in Figure 2, Cx50-Cx36N gap junction channels displayed non-inactivating junctional currents (I_js) in the V_js of ±20 to ±40 mV. When the V_js were in the range of ±60 to ±100 mV, a very slow I_j inactivation was observed, taking as long as 15 s to reach a steady-state. We calculated the coupling conductance (G_j) at the steady state and at the initial peak of the I_js, and normalized the steady-state G_j to the peak G_j to obtain G_j,ss. The G_j,ss − V_j relationship of Cx50-Cx36N was generated and was found to be very similar to that of Cx36 channels (Figure 2), indicating, as we anticipated that the NT domain is indeed very important in determining the G_j,ss − V_j relationship. We attempted to fit the data in the G_j,ss − V_j plots of both Cx36 and Cx50-Cx36N with the two-state Boltzmann equation, but the fittings could not converge. Thus, we only show the plot of G_j,ss − V_j on the averaged data for these two connexins.

Figure 2

To further identify the roles of the individual amino acid residues, especially the charged residues, we generated two single-point mutants (Cx50N9R and Cx50G8E) and a triple mutant (Cx50GNI). The net charge of the NT domain of these mutants was different, from −2 (Cx50N9R), −3 (Cx50GNI) to −4 (Cx50G8E) (see Figure 1C). Junctional currents (I_js) in response to V_js of ±20 to ±100 mV were recorded from N2A cell pairs expressing each of these mutants, and displayed together with those of wild-type Cx50 (the NT net charge is –3) (Figure 2, left panel). At V_js of ±20 mV, none of them showed much I_j inactivation. However, at V_js of ± 40 to ±60 mV, I_js of different mutants displayed different level of inactivation. In these mutants, the order of low to high level of inactivation of the I_js was Cx50N9R, Cx50GNI, Cx50, and Cx50G8E. At V_js of ±80 to ±100 mV, the inactivation of the I_js appeared to be constant in the following mutants: CX50GNI and Cx50G8E, and wild-type Cx50. Only Cx50N9R appeared to display further continued inactivation of I_js with the increased V_j. The G_j,ss − V_j relationships in both positive and negative V_js of these mutants and wild-type Cx50 could be nicely fitted by the Boltzmann equation and were plotted together in Figure 2 (right panel) for comparison.

In the positive V_js, the G_j,ss was in a high conducting state in the low V_j range. With the increase of the V_j, the G_j,ss became a much lower conducting state for each of the mutants. Mirror symmetrical V_j-dependent changes on G_j,ss were observed in negative V_js for these mutants, so that the two Boltzmann fits for each of the mutants showed Y-axis symmetrical “bell”-shaped curves. A two-state Boltzmann model provided parameters describing the fitted curves for each polarity of V_j. The definition of each Boltzmann parameters are listed as follows: G_max is the theoretical maximum gap junction conductance extrapolated from the experimental data; G_min is the extrapolated value of residual conductance; V₀ is the half-inactivation voltage at which G_j,ss = (G_max + G_min)/2 and A = zq/KT represents the voltage sensitivity (slope of the Boltzmann fitting curve) in terms of the number of equivalent gating charges, z, moving through the entire applied field, where q is the electron charge, and K and T are the Boltzmann constant and absolute temperature, respectively. One of these parameters, V₀, clearly correlated with the increase of the net negative charge of the NT domain.

With the increase of the net negative charges from −2 to −4, the absolute values of V₀ changed from 58–60 mV (Cx50N9R), 45–46 mV (Cx50GNI), 38–39 mV (Cx50) to 30–31 mV (Cx50G8E) (see Table 1 for details). Visually, the “bell” shaped Boltzmann fitted curves became narrower (Figure 2). Though our data on Cx36 and Cx50-Cx36N G_j,ss − V_j plots did not converge for Boltzmann fitting, previous studies on Cx36 channels showed a much higher V₀ of 73–78 mV (Srinivas et al., 1999b) and of 85–87 mV (Moreno et al., 2005), indicating that the Cx36 channels, and possibly the Cx50-Cx36N channels, possess a higher V₀. It is clear that with the increase in the net negative charge of the NT domain, the apparent V₀ value is decreasing in these studied Cx mutants/chimeras, although the magnitude of the V₀ change appears to be much more drastic with the net negative charge increase from −1 (Cx36 and Cx50-Cx36N) to −2 (Cx50N9R) than those V₀ changes with the increases from −2 to higher levels of negative charges (Cx50GNI, Cx50, and Cx50G8E). V₀ is a parameter describing the electrical field required to close 50% of the gap junction channels. A decrease in V₀ can be achieved via several ways: a decrease in the stability of the open state, an increase of the stability of the closed/residue states, or the combination of both.

Our experimental evidence indicates that the open dwell time is increased in Cx50-Cx36N, but decreased in Cx50N9R relative to that of wild-type Cx50 channels, which suggests that the open stability of the Cx50 gap junction channel is changed by these and possibly other studied mutants. More systematic studies are required to answer the question of whether the stability of the closed/residue states is also changed by these mutants.

Unitary channel properties of Cx50, Cx36, and Cx50 mutants/chimera

Cx50 gap junction channels displayed a large single channel conductance (γ_j = 200 pS) at the main conducting state (also known as main state) and one subconducting state (also called substate or residue state) of approximately 40 pS (Srinivas et al., 1999a). Cx36 channel-mediated unitary channel conductance was much lower. Srinivas and colleagues reported a main γ_j of 10–15 pS (Srinivas et al., 1999b) and Moreno measured an even lower γ_j of 5 pS in pancreatic β-cells of Cx36 channels (Moreno et al., 2005). We tried to resolve the γ_j in our recording system and found that Cx36 channel unitary current was buried into the baseline noise level beyond the resolution of our recording setup, suggesting that the γ_j of Cx36 could be even lower. The consensus of the literature is that the main γ_j of Cx36 is very low and that of Cx50 is high, which begs the question: what will happen to the mutants/chimera when single or multiple amino acid residues of the Cx36 NT are switched into the Cx50? It was fortunate that all the mutants/chimeras listed in Figure 1C showed readily measurable unitary currents in poorly coupled cell pairs without any pharmacological interventions.

Cx50-Cx36N channel showed low level γ_j of around 40 pS (Figure 3). The conductance was almost identical to the substate conductance of the Cx50 channel, which made us wonder if the Cx50-Cx36N channel locked the channel in a subconducting state equivalent to that of the substate of Cx50 channel. However, our subsequent work on heterotypic Cx50/Cx50-Cx36N channels argued against this possibility. In the heterotypic channels of Cx50/Cx50-Cx36N, both main and subconductance states were evident (Xin et al., 2012b). Therefore, the reason for not being able to detect a clear substate for the homotypic Cx50-Cx36N channel must be a tiny conductance (beyond detection) combined with extremely low dwell time at the substate.

Figure 3

Homotypic Cx50N9R channels displayed a higher level of γ_j (132 ± 4 pS) than that of Cx50-Cx36N channels, and no long-lived subconductance states were observed in all the tested V_js (Figure 3). The gating transition time between the open state and the fully closed state (the average of 10–90% rise or decay time is 5.7 ms) was significantly longer than the transition time of the open state to the substate of the Cx50 channels (typical value of 10–90% rise or decay is ≤1 ms) (Xin et al., 2012b). However, it was also shorter than the transition time defining the slow V_j-gating between the fully closed state to open/substate (~10 ms) of the Cx43 channels (Bukauskas and Peracchia, 1997).

The single channel currents recorded from the homotypic Cx50GNI and Cx50G8E channels were virtually identical to that of wild-type Cx50 channels. The main open state and subconductance state conductance of Cx50GNI (216 pS and 42 pS, respectively) and Cx50G8E (222 pS and 42 pS, respectively) were statistically the same as those of Cx50 channels (205 pS and 39 pS, respectively, Figure 3).

It is clear that the average of the main γ_j of the mutants/chimera increases with the increase of net negative charges at the NT domain. The γ_j range from below measurable level of Cx36 channels (with −1 at the NT domain), to a very low level of Cx50-Cx36N (−1) channels, an intermediate level of Cx50N9R (−2) channels to high level in Cx50GNI (−3), Cx50 (−3) and Cx50G8E (−4) channels. It appears that a saturation level for the main γ_j is reached when the net charge of the NT domain reaches −2 or lower. Our data are consistent with a structural model where the NT domain of Cx50 folds into, and lines, the initial portion of the gap junction pore. As the Cx50 channel is a cation preferred channel (Srinivas et al., 1999b), more negatively charged residues may help to attract more cations and increase the local cation concentration at the pore mouth (entrance), which would thus facilitate a higher rate of permeation through the gap junction channel. Conversely, reducing the net negative charge may alter the local charge density at the pore entrance and subsequently reduce the local cation concentrations. This may be the reason Cx50N9R and Cx50-Cx36N have a much lower γ_j than Cx50 channels. Interestingly, Cx50D3N also reduced the net charge of the NT domain and was found to decrease the single channel conductance of its hemichannels, which is consistent with our prediction (Peracchia and Peracchia, 2005; Srinivas et al., 2005).

Final remarks

Here we discuss the importance of net negative charges at the NT domain for the V_j-gating and γ_j. Our experimental evidence shows a good inverse correlation of the net negative charge with the value of the Boltzmann parameter, V₀. Additionally, a significant decrease of the net negative charge correlates with a decrease in the main γ_j. We acknowledge, however, that in addition to charge changes, many other factors, including the size, polarization and hydrophobicity of the side chains of the amino acid residues in the NT, and other domains lining the pore, can also play a role in determining the biophysical properties of the gap junction channel. One example we encountered was the mutation Cx50D3E, where there was no change in the net negative charge, but only a minor change in the side chain size. This mutant greatly changed the V_j-gating properties, with a substantial decrease of the gating charge (z), and the free energy between the open and closed states in the absence of the V_j. This mutant was also shown to reduce the γ_j (Xin et al., 2012a). We believe that this third residue of the NT domain may be critical for maintenance of the normal structure of the pore, where a small change in the side chain of the amino acid residue could induce a big conformational change of the channel. Although we have learned a great deal in the past 30 years about gap junction channels, we are only just beginning to understand the detailed structure-function relationship of gap junction channels. New experimental and structural model approaches are needed to address those unresolved questions surrounding the specific gap junction channel properties.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

• 1

  Al-UbaidiM. R.WhiteT. W.RippsH.PorasI.AvnerP.GomesD.et al. (2000). Functional properties, developmental regulation, and chromosomal localization of murine connexin36, a gap-junctional protein expressed preferentially in retina and brain. J. Neurosci. Res. 59, 813–826. 10.1002/(SICI)1097-4547(20000315)59:6<813::AID-JNR14>3.3.CO;2-R

  • CrossRef
  • Google Scholar

• 2

  BaiD.Del CorssoC.SrinivasM.SprayD. C. (2006). Block of specific gap junction channel subtypes by 2-aminoethoxydiphenyl borate (2-APB). J. Pharmacol. Exp. Ther. 319, 1452–1458. 10.1124/jpet.106.112045

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 3

  BarrioL. C.SuchynaT.BargielloT.XuL. X.RoginskiR. S.BennettM. V.et al. (1991). Gap junctions formed by connexins 26 and 32 alone and in combination are differently affected by applied voltage. Proc. Natl. Acad. Sci. U.S.A. 88, 8410–8414. 10.1073/pnas.88.19.8410

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 4

  BuhlD. L.HarrisK. D.HormuzdiS. G.MonyerH.BuzsakiG. (2003). Selective impairment of hippocampal gamma oscillations in connexin-36 knock-out mouse in vivo. J. Neurosci. 23, 1013–1018. Available online at: http://www.jneurosci.org/content/23/3/1013.full

  • Pubmed Abstract
  • Google Scholar

• 5

  BukauskasF. F.PeracchiaC. (1997). Two distinct gating mechanisms in gap junction channels: CO2-sensitive and voltage-sensitive. Biophys. J. 72, 2137–2142. 10.1016/S0006-3495(97)78856-8

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 6

  BukauskasF. F.VerselisV. K. (2004). Gap junction channel gating. Biochim. Biophys. Acta1662, 42–60. 10.1016/j.bbamem.2004.01.008

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 7

  BurtJ. M.SprayD. C. (1988). Single-channel events and gating behavior of the cardiac gap junction channel. Proc. Natl. Acad. Sci. U.S.A. 85, 3431–3434. 10.1073/pnas.85.10.3431

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 8

  ConnorsB. W.LongM. A. (2004). Electrical synapses in the mammalian brain. Annu. Rev. Neurosci. 27, 393–418. 10.1146/annurev.neuro.26.041002.131128

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 9

  DongL.LiuX.LiH.VertelB. M.EbiharaL. (2006). Role of the N-terminus in permeability of chicken connexin45.6 gap junctional channels. J. Physiol. 576, 787–799. 10.1113/jphysiol.2006.113837

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 10

  FooteC. I.ZhouL.ZhuX.NicholsonB. J. (1998). The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions. J. Cell Biol. 140, 1187–1197. 10.1083/jcb.140.5.1187

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 11

  GemelJ.LinX.VeenstraR. D.BeyerE. C. (2006). N-terminal residues in Cx43 and Cx40 determine physiological properties of gap junction channels, but do not influence heteromeric assembly with each other or with Cx26. J. Cell Sci. 119, 2258–2268. 10.1242/jcs.02953

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 12

  GongX. Q.NakagawaS.TsukiharaT.BaiD. (2013). A mechanism of gap junction docking revealed by functional rescue of a human-disease-linked connexin mutant. J. Cell Sci. 126, 3113–3120. 10.1242/jcs.123430

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 13

  GonzalezD.Gomez-HernandezJ. M.BarrioL. C. (2007). Molecular basis of voltage dependence of connexin channels: an integrative appraisal. Prog. Biophys. Mol. Biol. 94, 66–106. 10.1016/j.pbiomolbio.2007.03.007

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 14

  HormuzdiS. G.PaisI.LebeauF. E.TowersS. K.RozovA.BuhlE. H.et al. (2001). Impaired electrical signaling disrupts gamma frequency oscillations in connexin 36-deficient mice. Neuron31, 487–495. 10.1016/S0896-6273(01)00387-7

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 15

  KronengoldJ.SrinivasM.VerselisV. K. (2012). The N-terminal half of the connexin protein contains the core elements of the pore and voltage gates. J. Membr. Biol. 245, 453–463. 10.1007/s00232-012-9457-z

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 16

  LairdD. W. (2006). Life cycle of connexins in health and disease. Biochem. J. 394, 527–543. 10.1042/BJ20051922

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 17

  MaedaS.NakagawaS.SugaM.YamashitaE.OshimaA.FujiyoshiY.et al. (2009). Structure of the connexin 26 gap junction channel at 3.5 A resolution. Nature458, 597–602. 10.1038/nature07869

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 18

  MaedaS.TsukiharaT. (2011). Structure of the gap junction channel and its implications for its biological functions. Cell. Mol. Life Sci. 68, 1115–1129. 10.1007/s00018-010-0551-z

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 19

  MorenoA. P.BerthoudV. M.Perez-PalaciosG.Perez-ArmendarizE. M. (2005). Biophysical evidence that connexin-36 forms functional gap junction channels between pancreatic mouse beta-cells. Am. J. Physiol. Endocrinol. Metab. 288, E948–E956. 10.1152/ajpendo.00216.2004

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 20

  MullerD. J.HandG. M.EngelA.SosinskyG. E. (2002). Conformational changes in surface structures of isolated connexin 26 gap junctions. EMBO J. 21, 3598–3607. 10.1093/emboj/cdf365

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 21

  MusaH.FennE.CryeM.GemelJ.BeyerE. C.VeenstraR. D. (2004). Amino terminal glutamate residues confer spermine sensitivity and affect voltage gating and channel conductance of rat connexin40 gap junctions. J. Physiol. 557, 863–878. 10.1113/jphysiol.2003.059386

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 22

  NakagawaS.GongX. Q.MaedaS.DongY.MisumiY.TsukiharaT.et al. (2011). Asparagine 175 of connexin32 is a critical residue for docking and forming functional heterotypic gap junction channels with connexin26. J. Biol. Chem. 286, 19672–19681. 10.1074/jbc.M110.204958

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 23

  NicholsonB. J. (2003). Gap junctions - from cell to molecule. J. Cell Sci. 116, 4479–4481. 10.1242/jcs.00821

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 24

  PeracchiaC.PeracchiaL. L. (2005). Inversion of both gating polarity and CO2 sensitivity of voltage gating with D3N mutation of Cx50. Am. J. Physiol. Cell Physiol. 288, C1381–C1389. 10.1152/ajpcell.00348.2004

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 25

  PeracchiaC.WangX. G.PeracchiaL. L. (2000). Chemical gating of gap junction channels. Methods20, 188–195. 10.1006/meth.1999.0936

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 26

  Perez VelazquezJ. L.CarlenP. L. (2000). Gap junctions, synchrony and seizures. Trends Neurosci. 23, 68–74. 10.1016/S0166-2236(99)01497-6

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 27

  PerkinsG. A.GoodenoughD. A.SosinskyG. E. (1998). Formation of the gap junction intercellular channel requires a 30 degree rotation for interdigitating two apposing connexons. J. Mol. Biol. 277, 171–177. 10.1006/jmbi.1997.1580

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 28

  PurnickP. E.OhS.AbramsC. K.VerselisV. K.BargielloT. A. (2000). Reversal of the gating polarity of gap junctions by negative charge substitutions in the N-terminus of connexin 32. Biophys. J. 79, 2403–2415. 10.1016/S0006-3495(00)76485-X

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 29

  RubinJ. B.VerselisV. K.BennettM. V.BargielloT. A. (1992). A domain substitution procedure and its use to analyze voltage dependence of homotypic gap junctions formed by connexins 26 and 32. Proc. Natl. Acad. Sci. U.S.A. 89, 3820–3824. 10.1073/pnas.89.9.3820

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 30

  SaezJ. C.BerthoudV. M.BranesM. C.MartinezA. D.BeyerE. C. (2003). Plasma membrane channels formed by connexins: their regulation and functions. Physiol. Rev. 83, 1359–1400. 10.1152/physrev.00007.2003

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 31

  SimonA. M.GoodenoughD. A. (1998). Diverse functions of vertebrate gap junctions. Trends Cell Biol. 8, 477–483. 10.1016/S0962-8924(98)01372-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 32

  SohlG.WilleckeK. (2004). Gap junctions and the connexin protein family. Cardiovasc. Res. 62, 228–232. 10.1016/j.cardiores.2003.11.013

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 33

  SrinivasM.CostaM.GaoY.FortA.FishmanG. I.SprayD. C. (1999a). Voltage dependence of macroscopic and unitary currents of gap junction channels formed by mouse connexin50 expressed in rat neuroblastoma cells. J. Physiol. 517, 673–689. 10.1111/j.1469-7793.1999.0673s.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 34

  SrinivasM.RozentalR.KojimaT.DermietzelR.MehlerM.CondorelliD. F.et al. (1999b). Functional properties of channels formed by the neuronal gap junction protein connexin36. J. Neurosci. 19, 9848–9855.

  • Pubmed Abstract
  • Google Scholar

• 35

  SrinivasM.KronengoldJ.BukauskasF. F.BargielloT. A.VerselisV. K. (2005). Correlative studies of gating in Cx46 and Cx50 hemichannels and gap junction channels. Biophys. J. 88, 1725–1739. 10.1529/biophysj.104.054023

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 36

  SugaM.MaedaS.NakagawaS.YamashitaE.TsukiharaT. (2009). A description of the structural determination procedures of a gap junction channel at 3.5 A resolution. Acta Crystallogr. D Biol. Crystallogr. 65, 758–766. 10.1107/S0907444909014711

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 37

  TeubnerB.DegenJ.SohlG.GuldenagelM.BukauskasF. F.TrexlerE. B.et al. (2000). Functional expression of the murine connexin 36 gene coding for a neuron-specific gap junctional protein. J. Membr. Biol. 176, 249–262. 10.1007/s002320001094

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 38

  UngerV. M.KumarN. M.GilulaN. B.YeagerM. (1999). Three-dimensional structure of a recombinant gap junction membrane channel. Science283, 1176–1180. 10.1126/science.283.5405.1176

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 39

  VerselisV. K.GinterC. S.BargielloT. A. (1994). Opposite voltage gating polarities of two closely related connexins. Nature368, 348–351. 10.1038/368348a0

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 40

  VerselisV. K.SrinivasM. (2008). Divalent cations regulate connexin hemichannels by modulating intrinsic voltage-dependent gating. J. Gen. Physiol. 132, 315–327. 10.1085/jgp.200810029

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 41

  WaterhouseA. M.ProcterJ. B.MartinD. M.ClampM.BartonG. J. (2009). Jalview Version 2–a multiple sequence alignment editor and analysis workbench. Bioinformatics25, 1189–1191. 10.1093/bioinformatics/btp033

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 42

  WhiteT. W.GoodenoughD. A.PaulD. L. (1998). Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts. J. Cell Biol. 143, 815–825. 10.1083/jcb.143.3.815

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 43

  XinL.GongX. Q.BaiD. (2010). The role of amino terminus of mouse Cx50 in determining transjunctional voltage-dependent gating and unitary conductance. Biophys. J. 99, 2077–2086. 10.1016/j.bpj.2010.07.032

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 44

  XinL.NakagawaS.TsukiharaT.BaiD. (2012a). Aspartic Acid residue d3 critically determines cx50 gap junction channel transjunctional voltage-dependent gating and unitary conductance. Biophys. J. 102, 1022–1031. 10.1016/j.bpj.2012.02.008

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 45

  XinL.SunY.BaiD. (2012b). Heterotypic connexin50/connexin50 mutant gap junction channels reveal interactions between two hemichannels during transjunctional voltage-dependent gating. J. Physiol. 590, 5037–5052. 10.1113/jphysiol.2012.235507

  • CrossRef
  • Google Scholar