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editorial
. 2013 Feb 5;34(2):199–204. doi: 10.1038/aps.2012.202

Antibody therapeutics targeting ion channels: are we there yet?

Han Sun 1, Min Li 1,*
PMCID: PMC4011603  PMID: 23381110

Abstract

The combination of technological advances, genomic sequences and market success is catalyzing rapid development of antibody-based therapeutics. Cell surface receptors and ion channel proteins are well known drug targets, but the latter has seen less success. The availability of crystal structures, better understanding of gating biophysics and validation of physiological roles now form an excellent foundation to pursue antibody-based therapeutics targeting ion channels to treat a variety of diseases.

Keywords: ion channel, antibody, autoimmune neurological disorder, channelopathy, protein-based therapeutics

Introduction

Ion channels are a large family of membrane proteins that function by allowing ionic passage across cellular membranes. They are present in all cell types and play critical roles in a variety of biological processes. Among more than 429 annotated ion channel genes, many are important and validated therapeutic targets. Antibodies for ion channels are effective tools and widely used in various experimental settings. However, rarely have they been used to perturb ion channel function. So far no antibody-based drug on the market is targeted to an ion channel.

Epitopes on ion channels accessible by active antibodies

Patients with autoimmune disorders develop self-reacting antibodies. Some are autoantibodies against ion channels. Their roles in pathogenesis are implicated by correlation between antibody titer and severity of disease, effectiveness of plasma exchange, or immunosuppressive therapy. For example, paraneoplastic channelopathies are autoimmune neurological disorders that co-exist with tumors and tumor antigens are indicated as the trigger for autoantibody generation. In these instances, autoantibodies are utilized as diagnostic or prognostic markers for both neurological diseases as well as cancer (see review1). Indeed, many known autoimmune channelopathies involve antibodies that target voltage-gated ion channels. Mechanistic studies reveal that these antibodies can cause functional changes in ion channels that lead to clinical phenotypes. For example, Lambert-Eaton Myasthenic Syndrome (LEMS) is a disorder of neuromuscular transmission in which antibodies are directed to presynaptic voltage-gated calcium channels resulting in muscle weakness. Experimental evidence showed that bivalent antibodies were required for the overall reduction of acetylcholine release, supporting the notion that antibody-mediated cross-linking and subsequent internalization of channel protein leads to reduction in calcium influx2. Further investigation indicated that the LEMS patient-derived IgGs were capable of inhibiting P- and Q-type calcium currents specifically3.

Antibodies against voltage-gated potassium channels contribute to a broader range of autoimmune disorders, involving both the central nervous system and peripheral nervous system. In some patients with acquired neuromyotonia (NMT), also known as Isaac's syndrome, antibodies against voltage-gated potassium channels prevent membrane re-polarization, increase acetylcholine release, and prolong action potentials. The excess release of acetylcholine often leads to muscle twitching, cramps, stiffness, and abnormal muscle contraction and relaxation. Peripheral nerve hyper-excitability sometimes co-exists with effects in the central nervous system, including seizures, sleep disturbance, and behavioral changes. Treatments with patient antibodies led to a marked increase in compound action potential current and repetitive firing in isolated dorsal root ganglia (DRGs) similar to those observed with Kv channel blockers, such as aminopyridines4. Experimental evidence suggested that these antibodies act by inducing channel internalization5. Besides NMT, voltage-gated potassium channel antibodies have been detected in patients with cramp-fasciculation syndrome, limbic encephalitis (LE) and Morvan's syndrome (MoS). Immunohistochemical studies provided evidence that these autoantibodies display subtype-specificity. NMT and MoS antibodies bind preferentially to Kv1.2 and Kv1.6, whereas LE antibodies have a preference for Kv1.1. Difference in target specificity serves as one explanation for various clinical manifestations in these disorders6.

Besides paraneoplastic channelopathies, antibodies targeting ion channels have been associated with many other disorders including multiple sclerosis (MS). MS is the most common chronic inflammatory disease of the central nervous system. Although some patients are responsive to plasma exchange or B cell depletion by monoclonal antibodies, therapeutic outcome is often unpredictable due to unknown pathogenesis and clinical heterogeneity. Recently, Kir4.1 has been found to be the immune target in MS. Serum antibodies recognizing the first extracellular loop of Kir4.1 were detected in ∼50% MS patients compared to less than 1% of patients with other neurologic diseases. Injection of serum IgG resulted in a significant loss of channel expression and altered expression of glial protein along with complement activation in mice. It is likely that in addition to triggering immune responses, Kir4.1 antibodies could interfere with channel function leading to impaired axon myelination and tissue damage7.

Development of active antibodies

As early as three decades ago, active antibodies were generated and noted for their utility in functional studies of voltage-gated ion channels. Monoclonal antibodies (mAbs) were raised against membrane fragments from eel electroplax enriched for voltage-gated sodium channel8,9. Among these antibodies, three exhibited an effect on channel activity. SC-66-5 and SC-72-14 attenuated the action potential in rat nerve fibers by inhibiting depolarization and prolonging repolarization8. In follow-up studies, SC-72-14 was shown to alter the voltage-dependence of channel inactivation and inhibit sodium current10. When tested on canine cardiac fibers, SC-72-14 reduced Vmax and membrane responsiveness11. Another antibody, SC-72-38, enhanced the excitability of rat muscle cells by changing the voltage-dependence of sodium channel activation and inactivation. The observed changes were similar to those induced by Tityus serrulatus toxin γ (TiTXγ), and the binding of SC-72-38 and TiTXγ was mutually exclusive12. In another study, a mAb against dihydropyridine (DHP)-binding complex in rabbit muscle transverse tubules was generated and it suppressed the slow calcium current in a mouse muscle cell line. It also cross-reacted with sodium channel, shifting the voltage of activation threshold to a more positive value and slowing the rate of inactivation13,14.

To gain higher preference for subtype selectivity and harness the benefits of human genome sequence data, instead of injecting homogenized membrane fragments, synthetic peptides or recombinant proteins corresponding to a specific region in the channel are used to generate antibodies. Different regions in ion channels have been explored in rational target design for intended activity and specificity. For instance, regions in close proximity to the pore are of particular interest, since perturbation through antibody binding is likely to affect conductance. This strategy is supported by several studies. An antibody targeted at a region of the voltage-dependent calcium channel α1D subunit C-terminal to the pore-forming loop effectively reduced 30%–50% of native L-type calcium currents in DRG neurons and cardiac myocytes under depolarizing conditions15. Alternatively, antibodies can be generated against the small extracellular loop N-terminal to the pore-forming region. This region is extracellularly accessible and in many cases it displays considerable sequence variation, and thus may lead to the development of highly specific antibodies. This strategy, now known as E3 targeting (named after the third extracellular loop), was first examined in studies of voltage-gated potassium channels. Polyclonal anti-peptide antibodies that specifically recognized the E3 domain of Kv1.2 or Kv3.1 inhibited whole cell currents by more than 70% in neuronal cells with an IC50 value close to 60 nmol/L. Moreover, Kv1.2 antibody inhibited the binding of α-dendrotoxin, which is known to interact with Kv1.2 near pore region on the extracellular side16. Over the years, E3 targeting has been extended to investigation of several voltage-gated cation channels. For example, E3-targeted antibodies against Nav1.5 and TRPC5 inhibited whole cell currents up to 50%–60% in cells transfected with corresponding channels17. An anti-Kv1.2 antibody was able to restore consciousness of animals during anesthesia following thalamic microinfusion18. In a recent study, a polyclonal antibody was raised against the E3 domain in P/Q-type voltage-gated calcium channels. It effectively inhibited the function of N-type and P/Q-type calcium channels in cerebellar granule cells. Antibody binding abolished the effect of ω-conotoxin-GVIA which binds near to the pore. But it had no effect on ω-agatoxin-IVA that acts on a distal gating modality. When tested at neuromuscular junctions, this antibody attenuated excitatory postsynaptic currents. Moreover, cerebellum infusion caused cerebellar ataxia in mice, establishing a link between anti-voltage-gated calcium channel antibodies and pathogenesis19. Besides regulating neural excitability, some E3-targeted antibodies could modulate store-operated or agonist-evoked Ca2+ entry20,21,22,23,24,25, oligodendrocyte proliferation and migration26, and tumor growth27,28.

Channel regions that are not in the immediate vicinity of pore-forming region can be equally useful as active antibody targets. A polyclonal antibody directed to the voltage sensor of internal repeat I in sodium channel shifted the voltage dependence of fast current inactivation to a more negative value in cultured DRG neurons29. Moreover, it attenuated the action potential amplitude of rat sciatic nerves. Its binding to rat brain synaptosomes was enhanced by depolarization, suggesting a depolarization-induced conformational change that made the epitope more accessible to the antibody30. NESOpAb, an antibody directed to the second extracellular loop in Nav1.5 domain I, inhibited sodium currents up to 60% with an IC50 value of less than 25 nmol/L. It exhibited exquisite selectivity, distinguishing neonatal and adult splice variants which differ by seven amino acids only31. These studies suggest that ion channels possess many functional sites accessible to specific modulation by antibodies.

Active antibodies from bench to bedside

Antibodies constitute the fastest growing class of therapeutic agents. Antibody-based therapy has been well established to treat cancer, autoimmune and inflammatory diseases32,33. Although experimental evidences show that active antibodies can be utilized as research tools to modulate ion channel functions, their therapeutic application awaits further development. Despite experimental data, appropriate in vivo models need to be established to validate and characterize the functions of active antibodies in a defined biological context. Also, many active antibodies reported so far are polyclonal, which are usually not suited for therapeutic purposes. Generation of effective monoclonal antibodies is therefore essential for eventual clinical use. In addition, the structure and function of antibodies require fine tailoring to improve their pharmacological properties and safety. Various strategies and approaches have been developed for this purpose. Recombinant antibody fragments were created to ensure delivery across blood brain barrier (BBB) to target antigens in the brain34,35,36. New technologies are becoming more effective to enable antibodies to penetrate BBB37, including recent antibodies targeting beta-secretase (BACE1) for treating Alzheimer's disease38,39. Effector functions and plasma half-life of antibodies can be modified via engineering to meet different clinical requirements. Generation of humanized or completely human monoclonal antibodies with enhanced efficacy and safety is achievable via rational design and high throughput screens40,41. Although numerous challenges remain for applying active antibodies to treat human diseases, knowledge gained through ion channel active antibody research, and the availability of existing and emerging technologies to improve antibody performance will pave the way for development of future therapeutics.

Perspective

Antibodies recognizing ion channels, whether they have been generated intentionally by artificial immunization or unintentionally as results of autoimmune diseases, are effective in modulation of ion channel activity. The mechanisms of action include direct block of ion permeation pathway, modulation of ion channel gating, and internalization and degradation upon surface clustering (Table 1). The feasibility of developing active antibodies targeting ion channels combined with major advances in antibody technologies over the last decade promises that more effective antibodies may be available in the coming years. Their applications are likely to impact the development of therapeutics for a variety of diseases in which ion channels are validated targets.

Table 1. Summary of active antibodies for voltage-sensitive ion channels.

Channel family Antibody Region Epitope sequence Cell type Activities Reference
Voltage-gated potassium channels Anti-Kv 1.2 E3 extracellular loop in domain I FAEADERDSQFPSIP HEK-293 NG108-15 Central medial thalamus (rat) Reduce whole cell current Restore consciousness during anesthesia 16 18
Anti-Kv 3.1 E3 extracellular loop in domain I GAQPNDPSASEHTH HEK-293 NG108-15 Primary oligodendrocyte progenitor cell (mouse) Reduce whole cell current Reduce whole cell current; reduce proliferation and migration 16 26
Anti-Kv 10.1 Fusion of E3 extracellular loop in domain I and tetramerizing coiledcoil GSGSGKWEG HEK-293 Xenopus oocytes Neuroblastoma Breast carcinoma Melanoma Ovarian carcinoma Cervical carcinoma Pancreas carcinoma Colon carcinoma Fibrosarcoma Breast cancer xenograft Pancreatic cancer xenograft Acute myeloid leukemia SH-SY5Y MDA-MB-435s NCI-ADR HT144 C8161 SKMel2 SKOV3 SKOV6 OVCAR-3 OVCAR-8 HeLa BxPC3 HT29 HT1080 MDA-MB-435s Primary PAXF1657 HEL UT-7 K562 PLB-985 Primary cells Reduce whole cell current Reduce tumor growth Reduce proliferation and migration; increase cell death 27 28
Voltagegated sodium channels Anti-Nav (SC-72-14) Extracellular domain N/A Sciatic nerve fibers (rat) Optic nerve fibers (rat) Cardiac purkinje fibers (canine) Sciatic nerve fibers (rat) Reduce whole cell current; reduce action potential amplitude Reduce Vmax; reduce membrane responsiveness Reduce whole cell current; shift the voltage dependence of inactivation 8 11 10
Anti-Nav (SC-72-38) Extracellular domain N/A Myosacs (rat) Sciatic nerve fibers (rat) Shift the voltage-dependence of activation and inactivation Induce channel internalization 12 42
Anti-Nav (SC-66-5) Extracellular domain N/A Sciatic nerve fibers (rat) Optic nerve fibers (rat) Reduce whole cell current 8
Anti-Nav 1.5 E3 extracellular loop in domain I E2 extracellular loop in domain I CVRNFTALNGTNGSVEAD VSENIKLGNLSALRC HEK293 EBNA-293 Reduce whole cell current Reduce whole cell current 17 31
Voltage-gated calcium channels Anti-L-type Extracellular domain N/A BC3H1 myocytes (mouse) Reduce slow current 14
Anti-α1D C-terminal to the pore-forming region between S1 and S2 in domain IV KLCDPDSDYNPGEEYTC Dorsal root ganglion (rat) Cardiac myocytes (guinea-pig) Reduce L-type current (use dependent) 15
Anti-N and P/Q-type P/Q-type E3 extracellular loop DESKEFERDCRGK Cerebellar granule neurons (mouse) HEK293 Purkinje cell soma (mouse) Cerebellum (mouse) Reduce N-type current, P/Q-type current, excitatory postsynaptic current Induce cerebellar ataxia phenotype 19
Anti-P-type E3 extracellular loop IDVEDEDSDEDEFC Small-cell lung carcinoma H146 H209 H345 Reduce P-type current 43
TRP channels Anti-TRPC1 E3 extracellular loop QLYDKGYTSKEQKDC CVGIFCEQQSNDTFHSFIGT Platelets and vascular endothelial cells (human) Vascular smooth muscle cells (human) Bovine aortic endothelial cells Reduce agonist-evoked or store-operated calcium entry Reduce store-operated calcium entry Reduce store-independent, agonist-evoked calcium entry 20,23 21 22
Anti-TRPC5 E3 extracellular loop CYETRAIDEPNNCKG HEK293 CHO Cerebral arterioles (rabbit) Pial arterioles (rabbit) Reduce L-type current 17 24
Anti-TRPM3 E3 extracellular loop CLFPNEEPSWKLAKN HEK293 Reduce whole cell current 25
Anti-TRPV1 E3 extracellular loop EDGKNNSLPMESTPHKC RGSACKP CHO HEK293 Reduce channel activation by proton, heat and chemical ligands 44
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Acknowledgments

We thank members of the Li laboratory for valuable discussions, reviewers for helpful comments, and Alison Neal for editorial assistance. This work is supported by grants to ML from the National Institutes of Health (GM078579, MH084691) and Maryland Stem Cell Research Foundation (2010-MSCRFE-0164-00).

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