- Open Access
An overview of the potassium channel family
© GenomeBiology.com 2000
- Published: 13 October 2000
Potassium channels, tetrameric integral membrane proteins that form aqueous pores through which K+ can flow, are found in virtually all organisms; the genomes of humans, Drosophila, and Caenorhabditis elegans contain 30-100 K+ channel genes each. The structure of a bacterial K+ channel, sequence comparisons with other channels and electrophysiological measurements have enabled conclusions about the mechanism of gating and ion flow to be drawn for many other channels.
- Transmembrane Helix
- Channel Gene
- Aqueous Pore
- Backbone Carbonyl Group
- Direct Structural Information
Potassium channels, originally identified as the molecular entities mediating flows of potassium ions across nerve membranes in action potential generation, are now known in virtually all types of cells in all organisms, where they are involved in a multitude of physiological functions. They are tetrameric integral membrane proteins forming transmembrane aqueous pores through which K+ specifically permeates. Many molecular subfamilies of K+ channels are known, and these roughly correspond to the physiological signals by which pore opening is controlled, for example, voltage, Ca2+, G proteins, and polyamines. The high-resolution structure of a bacterial K+ channel is known, and this reveals the chemical basis of K+-selective permeation. The genomes of humans, Drosophila, and Caenorhabditis elegans contain 30-100 K+ channel genes each, and some of these are subject to elaborate alternative splicing. Several human genetic diseases, such as pathologies involving cardiac arrhythmias, deafness, epilepsy, diabetes, and misregulation of blood pressure, are caused by disruption of K+ channel genes. In this review I shall summarize what is currently known about the structure of these proteins and the genes encoding them, their evolution, the mechanism by which they transport ions, and the various physiological functions they fulfill.
The evolution of K+ channels is a subject of much speculation, but the appearance of this family throughout the biological universe suggests that they are ancient proteins, not the highly specialized neuro-machines that were envisioned when they were originally described . All fully sequenced genomes - eukaryotic, eubacterial, and archaeal - contain at least one K+ channel . No other ion channel type displays such ubiquity. K+ channels are the founding members of the 'S4-superfamily' of ion channels dedicated to electrical signaling, which, apart from the K+ channels, are found exclusively in eukaryotes. The cyclic nucleotide-gated channels evolved from K+ channels via acquisition of a cyclic nucleotide-binding domain near the carboxyl terminus; the Ca2+ and Na+ channels, each of which is a monomer containing four internal repeats, evolved from K+ channels via two gene duplications, with the Ca2+ channels appearing in unicellular organisms such as protists, and Na+ channels arising with the appearance of neurons in multicellular organisms. The pore-forming sequences of these neuronally specialized channels evolved to achieve alternative ion specificities.
In humans, many but not all K+ channel genes are multiply spliced. Not enough is yet known to make generalizations about gene structure; in some cases, the entire coding region lies within a single exon, while in others it is segmented into multiple exons, which in some but not all instances delineate clear functional domains. K+ channel genes are in general not chromosomally clustered.
There are two broad classes of K+ channels defined by transmembrane topology, as reflected in primary sequence: the six-transmembrane-helix voltage-gated (Kv) and the two-transmembrane-helix inward-rectifier (Kir) subtypes [3,4,5] (Figure 1). All K+ channels display a 'signature sequence' between the two most carboxy-terminal transmembrane helices , which reads, with minor variations, TMxTVGYG (using the single-letter amino acid code). In addition, all Kv-type channels have a highly unusual 'S4 sequence' in which lysine or arginine appears in every third or fourth position in an otherwise hydrophobic stretch making up the fourth transmembrane segment [3,4]. Several variations on these gross sequence features are known; the 'slowpoke' subfamily of Ca2+-activated K+ channels, which are architecturally similar to the Kv subtype, has an extra transmembrane segment near the amino terminus, and the '2P' channels have subunits that are tandem pairs of two K+ channel sequences. (Most 2P channels are formed from pairs of Kir-like sequences, but a few are known in which a Kv-type and a Kir-type are linked in tandem.)
Currently, direct structural information of K+ channels is limited to a single bacterial protein, KcsA, of Kir topology  (Figure 2). But the structural inferences drawn from electrophysiological experiments on eukaryotic K+ channels are in such striking harmony with the bacterial channel structure that it is safe to extrapolate the following structural features from KcsA to the entire family. K+ channels are formed as tetramers  of identical or similar subunits arranged in fourfold symmetry around the water-filled ion-conduction pathway (except for the 2P tandem channels, which are presumably dimers.) Common to all K+ channel subunits is a structural core consisting of two transmembrane helices, readily identified by hydrophobicity algorithms, separated by a re-entrant pore-loop carrying the signature sequence (Figure 1). The most carboxy-terminal transmembrane helix and the signature sequence form most of the lining of the aqueous pore and thus carry the structural determinants of the high K+ selectivity exhibited by most K+ channels [6,9,10]. The transmembrane span of the aqueous pore of KcsA, and by inference of other K+ channels, is highly asymmetric. The narrowest part of the pore, the 'selectivity filter', is a 3 Å diameter tube originating abruptly on the extracellular side of the protein and extending normal to the membrane plane for about 10-15 Å. The wall of this structure is uncharged but highly hydrophilic, lined mainly by twelve backbone carbonyl groups, three from each subunit. The pore then widens to a 10 Å spherical water-filled cavity about halfway through the membrane. This cavity's wall, constructed mostly from aliphatic sidechains, is counterintuitively hydrophobic in nature, as is the intracellular end of the pore. In the KcsA structure (Figure 2), the pore is occluded on the intracellular side by the crossing of four of the transmembrane helices in a 'teepee'-like structure; this occlusion region almost certainly represents the closed state analogous to the 'gate' of the Kv channels, the conformational switch known to open and close the pore. In both Kv and Kir topology, both the amino and carboxyl termini are located on the cytoplasmic side of the membrane.
In the six-transmembrane Kv channels, the first four transmembrane segments, S1-S4, form a module that somehow controls the opening and closing of the pore (Figure 3). The first three of these segments are inferred to be helical along most of their lengths and located on the lipid-exposed periphery of the membrane-embedded complex. The fourth transmembrane segment, S4, which is not lipid-exposed, is thought to form the voltage-sensing element of these channels. This S4 sequence also is found in several classes of channels that have little or no voltage-dependent gating, such as Ca2+-activated K+ channels and cyclic nucleotide-gated channels.
K+ channels are found in so many different types of cells carrying out so many different biological tasks that it is impossible to summarize all of them here. All K+ channels, however, carry out a single basic function: the formation of a transmembrane 'leak' extremely specific for K+ ions. Since cells almost universally maintain cytoplasmic K+ concentrations much higher than those extracellularly, the opening of a K+ channel automatically implies a negative-going change in electrical voltage across the cell membrane. This 'membrane hyperpolarization', as it is known in the technical jargon, occurs in different physiological contexts for varied purposes. Obvious examples involve termination of the action potential in electrically excitable cells such as nerve, muscle, hormone-secreting adrenal chromaffin, and pancreatic β cells. But more subtle functions are known in non-excitable cells. K+ channels play crucial roles in the cellular K+ recycling required for electrolyte balance effected by the renal epithelium; hyperpolarization of T and B cells is a prerequisite for mitogenesis and proliferation in the immune response; the electrical tuning of mechanosensory cells in auditory transduction relies centrally on the gating kinetics of K+ channels; guard cells from green plants rely upon K+ channels to regulate osmotic flow required for regulation of gas and water exchange in leaves; even erythrocytes, often viewed as passive bags of hemoglobin, use a K+ channel, probably for volume regulation and maintenance of cell shape. The biological functions of prokaryotic K+ channels are unknown.
In general, K+ channel activities are elaborately and tightly regulated, both by tissue-specific control of transcription and by biochemical actions on the channel proteins. Some K+ channels are constitutively active, but most act transiently, being 'gated' by physiological signals. The Kv channels are activated by depolarizing voltage changes; some Ca2+-activated K+ channels are sensitive to both voltage and cytoplasmic Ca2+ levels, whereas others respond only to Ca2+; different classes of Kir channels are directly gated by intracellular factors such as G proteins, nucleotides, or polyamines. In addition, protein phosphorylation is often found to modulate the sensitivity of K+ channels to their primary physiological signals, or is itself the activating signal .
The most fundamental task carried out by all K+ channels is to catalyze the rapid permeation of K+ ions while rejecting biologically abundant potential competitors such as Na+, Ca2+, and Mg2+. The general mechanistic outlines of how these proteins manage to select with high efficiency the larger potassium ion over the smaller sodium ion have been known for decades [16,17], and the recent structure of KcsA provides the molecular details of this catalytic mechanism . There are two features essential to achieving the combination of exquisite ion selectivity and high throughput rate of K+ channels: first, precise co-ordination of dehydrated K+ by the protein; second, multiple ion occupancy within the permeation pathway. The basic idea is that K+ channel pores present electronegative oxygen moieties - now known to be mainly backbone carbonyl groups of the signature sequence - arranged as a cage into which a dehydrated K+ ion exactly fits, but in which a Na+ ion would fit so loosely that it energetically prefers to remain in aqueous solution. In other words, K+ binds tightly to the pore. This feature alone would produce high selectivity for K+, but it would not allow high throughput because the tightly bound ion would dissociate from its site very slowly. To achieve a fast dissociation rate, three ion-binding sites lie in single file within the pore, close enough that the ions electrostatically repel each other.
Although no high-resolution structures of Kv channels are known, some basic characteristics of the gating of these voltage-dependent channels are understood. The central event initiating channel opening is an outward movement of the S4 transmembrane segment, as depicted in Figure 3b; since this segment carries numerous positively charged residues, this conformational movement is energetically favored by depolarizing voltage [19,20]. How this movement is actually coupled to the opening of the pore, however, is still unknown. It is known, however, that opening of Kv channels is the direct result of movements of S6 near the intracellular end of the pore .
Another type of gating seen in some Kv channels is termed 'N-type inactivation', a process leading to the spontaneous closing of the channel upon maintained depolarization. The conformational change producing this inactivation involves the physical plugging of the intracellular end of the open pore by the channel's amino-terminal 20 or so residues, which act as a tethered pore-blocker in a 'ball-and-chain' mechanism [22,23].
Two broad areas of K+ channel research are beginning to yield to modern experimental assault: molecular structures of the proteins, and the mapping of specific K+ channel proteins to cellular and physiological contexts. Each of these areas has presented vexing, difficult barriers, which are now being overcome. Structural efforts are directed towards overexpression of prokaryotic K+ channels, which when successful can lead quickly to crystallographic and spectroscopic investigations of the purified protein. In addition, several isolated water-soluble domains and associated sub-units of eukaryotic K+ channels have been crystallized, and full-length channels are being modeled by piecing together these separate structural elements. The overexpression and crystallization of full-length eukaryotic K+ channels is still beyond the reach of current techniques, but cryo-electron microscopy and single-particle image reconstruction algorithms are starting to provide low-resolution (about 20 Å) structures of ion channels.
The cell biology and physiology of K+ channels presents great challenges for the future. Since several K+ channel sub-units are typically expressed in an individual cell, and since subunits within the same subfamily can co-assemble into the same tetramer, the collection of K+ channels in a given tissue is almost certainly highly heterogeneous. What is the composition of K+ channels in a given cell? Does the cell regulate K+ channel function by controlling the mix of subunits available for tetramer assembly? Are K+ channel subunits segregated within a cell by scaffolding proteins? As molecular probes for K+ channels become more sophisticated, it will be possible to answer difficult questions like these.
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