Polypeptides from animal venoms have found important uses as drugs, pharmacological tools, and within biotechnological and agricultural applications. We here report a novel family of cystine knot peptides from nemertean worms, with potent activity on voltage-gated sodium channels. These toxins, named the α-nemertides, were discovered in the epidermal mucus of Lineus longissimus, the ‘bootlace worm’ known as the longest animal on earth. The most abundant peptide, the 31-residue long α-1, was isolated, synthesized, and its 3D NMR structure determined. Transcriptome analysis including 17 species revealed eight α-nemertides, mainly distributed in the genus Lineus. α-1 caused paralysis and death in green crabs (Carcinus maenas) at 1 µg/kg (~300 pmol/kg). It showed profound effect on invertebrate voltage-gated sodium channels (e.g. Blattella germanica Nav1) at low nanomolar concentrations. Strong selectivity for insect over human sodium channels indicates that α-nemertides can be promising candidates for development of bioinsecticidal agents.
Peptides and proteins originating from animal venoms and toxins are intriguing sources of bioactive compounds. Some toxins have found their way to the market as drugs or pharmacological tools1, and others are finding applications in biotechnology and agriculture2. Snakes, scorpions, spiders, lizards, centipedes, and cone snails are all known producers of peptide toxins, but there are other classes of organisms for which the chemistry largely remains unknown. In the current work, we have explored one such neglected source of toxins: the nemerteans or ribbon worms.
Nemerteans have striking similarities with cone snails; both phyla use a proboscis for capture of prey, and one sub-class of nemerteans is also equipped with a stylet having the same apparent function as the radula tooth of the cone snail: venom injection. However, it is the mucus that covers the epidermis of nemerteans that appears to be the most conspicuous source of chemistry of these animals. Early indications of the bioactivity of the mucus have been attributed to the presence of low molecular weight toxins, including pyridyl alkaloids such as anabaseine3, and tetrodotoxin4.
In comparison, the interest in protein or peptide toxins from nemerteans has been sparse. Reports are confined to the cytolytic 10 kDa “A-toxins”, the 6 kDa neurotoxic “B-toxins” isolated from the mucus of the milky ribbon worm, Cerebratulus lacteus5, and the 10 kDa parborlysins that were discovered in Parborlasia corrugatus6. The molecular targets of these possible peptide toxins are yet unknown.
The Nemertea phylum comprises approximately 1300 species. Lineus longissimus, the bootlace worm, is known as the longest animal on earth with a body length of up to 50 m (Fig. 1). This species belongs to the anoplan nemerteans, carrying a proboscis without a stylet. This marine worm is found in the northern hemisphere at the intertidal sea bottom; on the Swedish west coast it is found from 10 m depths and below. L. longissimus first sparked our interest as a possible source of tetrodotoxin (TTX). However, TTX could never be identified, but the mucus still showed potent activity when injected into the branchial chamber of green crabs (Carcinus maenas)7. Instead, as shown in the current work, the activity is explained by the presence of a novel family of disulfide-rich peptide toxins.
LC-MS analysis and MALDI-MSI show peptides in the mucus of Lineus longissimus
Specimens of Lineus longissimus were collected off the Swedish west coast, and kept alive in the laboratory. When provoked, this ribbon worm releases substantial amounts of mucus; this mucus was collected and lyophilized. After redissolving and desalting of the sample using gel filtration, HPLC and LC-MS analyses of the mucus (Fig. 2A) revealed three prominent peptide peaks with mass-to-charge (m/z) ratio (M + H+) of 3308.35, 3260.40 (mo.) and 6419.00 (av.) (Fig. 2B). These compounds were then isolated in µ-gram amounts using a combination of gel filtration and RP-HPLC. Matrix assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) analysis of cross sections demonstrated that the peptides are confined to the epidermis and to the mucus layer of the worm, Fig. 2C.
Sequencing of nemertide peptides α-1 and α-2
Isolated and purified peptides were reduced and alkylated, and the shifts in total mass demonstrated that the 3 kDa peptides contain three and the 6 kDa peptide four disulfide bonds. Quantitative amino acid analyses indicated that the 3 kDa peptides, named nemertide α-1 and α-2, are closely related. The 6 kDa peptide, which is distinct, was named nemertide β-1. For the α-family, experimental masses of both peptides differed from the masses calculated from amino acid analyses by 32 Da, suggesting further posttranslational modifications in addition to disulfide bond formation. Alkylated peptides were digested to generate fragments amenable for de novo sequencing using data from LC-MSMS, which resulted in the sequence for 20 out of the 31 amino acids to be successfully determined for α-1 and α-2 (Fig. 3).
In order to identity the missing segments, the transcriptome of L. longissimus was sequenced from RNA isolated from transversal dissections along the body of a single specimen. The assembled transcriptome contains 81597 contigs, with a total length of 91,851,747 bp. tBLASTn searches using the partial α-1 and α-2 sequences allowed identification of the full-length sequence of α-1. The full length of α-2 was subsequently identified using the transcriptome reported earlier by Whelan et al.8, confirming that the difference is confined to a single amino acid substitution of a Val to Phe. The combination of MSMS sequencing, amino acid analyses and transcriptome data suggested that the posttranslational modification involves hydroxylation of both Pro28 and Pro29, which explains the mass difference of 32 Da.
Transcriptome analyses reveal α-, β-nemertides, A-toxins and parborlysins in nemerteans
The sequence of nemertide β-1 was also determined using transcriptome data. It comprises 57 amino acids, four disulfide bonds, and two hydroxyprolines (Hyp), and shows homology to neurotoxin B-II9. The transcriptomes of 17 species were subsequently analyzed for the presence of nemertides (Table S1). Seven complete α-nemertide sequences were discovered, all from the genus Lineus (Fig. 3), and one partial sequence from Riseriellus occultus. All α-nemertides discovered so far are from species within Heteronemertea, and no homologous sequences to α-nemertides were found in any other organisms.
The transcriptomes were also searched with queries for homologues to β-nemertides, A-toxins, parborlysins, and possible processing enzymes. Nemertide β-1 as identified in the L. longissimus transcriptome by matching MSMS data that was used as query together with the previously reported neurotoxin BII and BIV sequences. Eight additional β-nemertides (Figure S1A) were identified. Compared with α-nemertides, β-nemertides show a larger sequence variation, with an overall similarity of 51%. The A-toxin III (cytolysin A-III) has a sequence similarity with parborlysins 1–7 with a pairwise identity between 66.7 and 80.4%. In addition, 25 parborlysin homologues were found in addition to the seven sequences known previously (6) (Figure S1B). Interestingly, sequences resembling the proposed peptide maturation enzyme tex-31 from Conus textile were found in the L. longissimus transcriptome (Figure S2). Tex-31 cleaves a conotoxin propeptide with two basic residues in P1 and P2 positions, and preferably a leucine in P4 position10; its presence and likely processing site on the N-terminal side of mature α-1 nemertides suggests a possible common initial post-translational processing pathway.
Synthesis and NMR structure of nemertide α-1
Nemertide α-1 was selected as a target for further characterization of the structural and functional features of this novel family of peptides. To obtain peptide in sufficient amounts for structural and biological characterization we turned to peptide chemical synthesis. Nemertide α-1 was assembled using FMOC solid phase peptide chemistry. The peptide was cleaved from the resin, yielding reduced linear α-1 as the main product (Figure S3A). Peptide could then be oxidatively folded, to a homogenous chromatographic compound. Co-elution studies using reverse phase HPLC demonstrated identical folds of synthetically produced and folded α-1 and the isolated native peptide (Figures S3B,C).
The three-dimensional structure of α-1 was then determined using solution 2D NMR spectroscopy11 of the synthetic peptide. Overall, spectra were of excellent quality with well-dispersed signals indicating a defined structure (statistical data in Table S2). α-1 adapts a compact fold around the three disulfides located at the core of the molecule (Fig. 4). The disulfides form an inhibitor cystine knot (ICK) motif with a connectivity of Cys2-Cys16, Cys9-Cys20, and Cys15-Cys26. Sequence loops between cysteines are exposed at the surface of the molecule. The N-terminus is stabilized by the Cys2-Cys16 disulfide, whereas the C-terminus appears to be more flexible. The two Hyp residues are located in the C-terminal region. A short α-helix in the loop between Cys9 and Cys15 is the only element of regular secondary structure besides a series of tight turns. The two α-nemertides isolated from L. longissimus differ only by a Phe to Val substitution at position 8, which, together with Phe 22 and Trp 28, make up a surface exposed hydrophobic patch. In the family of α-nemertides, positions 4, 8 and 25 are subjects to variations. These residues are all displayed at the same side of the molecule. In analogy to other peptide toxins, these structural variations may control target preferences.
Structural alignment of α-1 using the DALI server12 identified human liver expressed antimicrobial peptide-2 LEAP-2 as the closest structural match with respect to Z score (Z: 3.7; rmsd: 1.1 Å; 21% sequence identity), followed by two ICK spider toxins, ω-HXTX-Hv1a (Z: 3.4; rmsd: 0.8; 30% sequence identity) and κ-TRTX-Scg1a (Z: 3.3; rmsd: 1.6; 20% sequence identity), Fig. 4D.
Nemertide α-1 induces paralysis in green crabs and cockroaches
To deduce the biological function of α-nemertides we used an established model organism to study toxicity of nemertean mucus in vivo: the green crab Carcinus maenas5,7. This model has biological significance because crustaceans are both well-known preys and possible predators of nemerteans13. Injection of α-1 into green crabs resulted in tremor of the limbs within 1–2 minutes, followed by hypertonus and paralysis. After 20–30 minutes, hypertonus was released while paralysis remained. Paralysis occurred from 1 µg/kg while doses of 10 µg/kg led to death within minutes (Fig. 5). A complementary experiment was carried out on 50 specimens of juvenile Blaptica dubia cockroaches (Table S3). Injections of α-1 resulted in a similar response to that of the green crabs: after 24 hours, death or permanent paralysis was observed for all animals at doses higher than 7.1 µg/kg.
Voltage-gated sodium channels are the targets of nemertide α-1
The rapid and potent paralytic effect of α-1 on C. maenas, the similarity of this effect to that of tetrodotoxin14, and the fact that ion channels are the most prominent targets of peptide toxins2, suggested that nemertide α-1 might assert its action by targeting voltage-gated sodium channels. Thus, synthetic α-1 was screened against three invertebrate and five vertebrate voltage-gated sodium channel isoforms (NaVs). Indeed, α-1 demonstrated a profound effect on the inactivation of invertebrate NaV channels of Blattella germanica (BgNaV1), Drosophila melanogaster (DmNaV1) and Varroa destructor (VdNaV1) (Fig. 5). At 1 µM, α-1 completely inhibited their inactivation, resulting in sustained non-inactivating currents. The activity of α-1 was characterized in further details on BgNaV1 and its EC50 potency at the channel was found to be 8.6 ± 2.9 nM. Addition of 10 nM α-1 gave no significant alteration of activation, whereas for the inactivation curves, V1/2 shifted from −60.4 ± 0.6 mV in the control to −54.5 ± 1.6 mV in the presence of peptide. Furthermore, α-1 significantly enhanced the recovery from inactivation (Figure S4A), and pulsing experiments demonstrated that the open state is not required for the toxin to interact with the channel (Figure S4B). At the mammalian NaVs α-1 was found to be significantly less potent. Nonetheless, 6 µM nemertide α-1 delayed the inactivation of human NaV1.1, NaV1.4, NaV1.5 and NaV1.6, whereas no effect was seen on NaV1.8. The EC50 on NaV1.6 was determined to be 0.8 ± 0.1 µM (Figure S4C), highlighting that α-1 shows ~100-fold selectivity towards insect NaVs over tested mammalian NaVs. These data are encouraging for the further exploration of α-1 as a bioinsecticide.
In the current work we report the discovery of a new family of peptide toxins from nemertean worms. Eight homologous individual peptides were identified on peptide and/or transcriptome level. All but one peptide contain 31 amino acid residues, including three disulfide bonds arranged in an ICK motif. The sequences determined share less than 50% similarity with any yet described peptide. These so called α-nemertides were initially found at the peptide level in Lineus longissimus. The mucus of this species has strong effect in the green crab assay, which is explained by the high potency of the prototypic isolated peptide. The effect is striking, but to fully appreciate the potency it should be put into context and compared to peptides from other venomous animals against their target species. Among the arthropods, spiders are a rich source of peptide toxins targeting insects, and there is a growing interest in using these toxins for the development of bioinsecticides. The most potent of those toxins are active in the range of 10–100 pmol/g2,15,16. In comparison, the active dose of α-1 at 1 µg/kg is equivalent to 300 fmol/g, highlighting the extraordinary potency of α-1. The fact that similar effect at a similar range (7.1–14.7 µg/kg) was observed upon injection in Blaptica dubia cockroaches, suggests that α-1 might be a suitable framework for development of novel bioinsectides. Indeed, ICK peptides have recently been introduced for that purpose on the agricultural market17.
The prototypic nemertide α-1 was shown to exert its neurotoxic activity by slowing down the inactivation of NaV channels, inducing a change of the steady-state inactivation without significant changes in the activation process. Upon binding, α-1 delays the recovery from inactivation. Furthermore, α-1 interacts with the NaV channels in the closed state. The α-1 induced alterations of gating kinetics resemble the effects of other peptide toxins known to be binding to the so-called neurotoxin binding site 318,19. Such toxins trap the voltage-sensing segment S4 of domain 4 in its inward or deactivated position, preventing fast inactivation20,21. Several toxins capable of binding to site 3 have been isolated from marine organisms22. Among these are the sea anemone toxins ATX-II and anthopleurin A that similarly act on NaV channels, and like α-1 exert anti-insect specificity as demonstrated by the complete inhibition of the inactivation of the insect NaV channels DmNaV1 and BgNaV1. However, additional experiments are needed to determine if site 3 is the target of α-1, for example competition experiments with known binders to that site.
Although the sequences of α-nemertides are unique, the ICK motif is shared with many other peptides, including toxins from spiders and cone snails and antimicrobial peptides. However, the closest 3D structural match is not an ICK peptide but LEAP-2. Backbone similarity of LEAP-2 and α-1 is striking, but LEAP-2 contains two disulfides only and patterns of surface hydrophobicity do not overlap. The physiological function of LEAP-2 is not clear23. Next structural matches are both spider toxins targeting voltage-gated calcium channels (ω-HXTX-Hv1a)24 and voltage-activated potassium channels (κ-TRTX-Scg1a)25. ω-HXTX-Hv1a belongs to the ω-atracotoxins, a family of arthropod-selective spider toxins initially characterized as selective insect CaV channel blockers. ω-HXTX-Hv1a has never been investigated for its activity on NaV channels. However, it should be noted that ω-HXTX-Ar1a, which shares 84% identity with ω-HXTX-Hv1a, does block insect NaV channels at higher concentrations (1 µM, 18% block)26. Together, this highlights how conserved folds and frameworks can adapt to different targets.
In comparison to other peptide toxins, the size of the peptides, the conserved ICK motif, and the origin and physiology of the expressing organism all draw clear parallels to cone snail toxins. In addition, sequences similar to the proposed peptide maturation enzyme tex-31 from Conus textile10 could be identified in the L. longissimus transcriptome (Figure S2). However, there are also profound differences: α-nemertides, despite their conserved structure, show little sequence similarity to any other peptide or protein, and whereas cone snail venoms contain complex libraries of hundreds to thousands of different peptides27, only two α-nemertides could be identified on peptide and RNA level in L. longissimus. In all, only eight different α-nemertide sequences could be identified from 17 transcriptomes, with no species expressing more than three variants. This is in stark contrast to the cocktails of toxins expressed by many other venomous animals, suggesting differences in the evolutionary pressure that have driven the expansion of the toxin repertoire in for example cone snails in which specialized sets of toxins are even used for capture of prey and for defense28. To us, the occurrence of the low number of toxins in e.g. Lineus longissimus suggests that they have a highly specialized function for the worm.
Whether α-nemertides are used for defense or capture of prey remains in question. The potent effect in the green crab assay does not exclude either explanation13,29 as crustaceans might be both prey and predator of nemerteans. In is noteworthy that selectivity differs between the toxins of cone snails and ribbon worms: whereas many cone snail peptides potently target vertebrate ion channels—and indeed are extensively pursued as clinically useful therapeutics—nemertide α-1 preferentially targets invertebrates. The further exploration of the Nemertea phylum may reveal further diversity in structures and activities among these toxins. To date, only a small fraction of the phylum has been investigated (the 17 species represent 1.5% of the known nemertean species).
The transcriptome analyses also revealed the presence of other peptide toxins, including novel parborlysin homologues. These are the first peptides of that family not originating from Parborlasia corrugatus, which has given these peptides their names. In the current work, we suggest the term “nemertides” as a general name for nemertean peptides, given the limited knowledge of their function, distribution and diversity. Moreover, because the physiological roles of neither the 3 kDa nor the 6 kDa nemertides reported here have yet been fully elucidated, we named peptide families α and β based on sequence similarities followed by a number indicating the order of discovery).
Bioinformatics was critical for the discovery of nemertides, but the key was the combination with biochemical analyses. This includes the extraction of peptides and analyses using chromatography and mass spectrometry. The prototypic α-1 peptide of this novel family was characterized with regard to structure and function, revealing striking activity on invertebrate voltage-gated sodium channels. In addition, the presence of these peptide toxins explains the bioactivity of the mucus previously attributed to TTX.
The results provide insight into the biological function of this new family of ICK peptides, and into the unknowns of chemical ecology of marine invertebrates. Indeed, nemertide α-1 is one of the most potent insecticidal peptides yet discovered, as judged by the activity on cockroach Navs, indicating a potential use of α-nemertides in the development of novel insecticides.
Materials and Methods
Collection of Lineus longissimus
Living specimens were collected at the west coast of Sweden (Kosterfjord, 35 m depth) and identified by Dr Malin Strand. Specimens were placed in a beaker containing seawater, and released mucus was collected after gently agitating the animal with a glass rod. One specimen was cut into pieces, which were either flash-frozen in liquid nitrogen or placed in RNA-later® solution.
Lyophilized mucus was dissolved in 30% acetonitrile (AcN) in water and 0.1% formic acid (FA), and desalted using size exclusion chromatography (SEC; PD-10, GE Healthcare). The eluate was lyophilized and redissolved in 10% AcN, 0.1% FA, and subjected to RP-HPLC on a Phenomenex Jupiter column (5 µ C18 300 Å, 250 × 4.6 mm) using a Shimadzu LC20 system. The gradient ranged from 5 to 55% AcN, in 0.05% trifluoroacetic acid (TFA).
Dry, reduced and alkylated peptide was cleaved using trypsin, chymotrypsin or endoproteinase Glu-C, in separate experiments, Fig. 3. Peptides were analyzed using a UPLC-QToF nanospray MS (Waters nanoAcquity, QToF Micro; 75 µm × 250 mm 1.7 µm BEH130 C18). Scan window was set to 200–2500 m/z and for MSMS to 50–2000 m/z.
Total RNA analysis
Total RNA was extracted from both flash-frozen and samples stored in RNAlater®, using Qiagen AllPrep DNA/RNA Mini Kit. The combined total RNA was sequenced using Illumina HiSeq. 2000 based RNA-seq paired end analysis and assembled by using Trinity (v 2011-11-26)30 (Macrogen, Korea).
Flash frozen tissues were cut (14 μm) using a cryostat-microtome (Leica CM3050S; Leica Microsystems, Welzlar, Germany), and thaw-mounted onto conductive indium tin oxide glass slides (Bruker Daltonics, Bremen, Germany). Sections were dried under a flow of nitrogen and desiccated at room temperature for 15 min, coated with 2,5-dihydroxybenzoic acid (35 mg/ml in 50% AcN, 0.2% TFA) before analysis using MALDI-TOF/TOF (Ultraflextreme, Bruker Daltonics). The Smartbeam II 2 kHz laser was operated in positive ion mode. Purified α-1, α-2 and β-1 were spotted on one section as an in-situ reference.
Nemertide α-1 was assembled on TentaGel XV HMPA resin (0.05 mmol scale) using Fmoc-based solid-phase peptide synthesis (SPPS). The C-terminal residues HypHypAsnGln and the dipeptide Fmoc-Leu-Ser(ψMe,MePro)-OH in position 11–12 were coupled manually, the latter to prevent peptide chain aggregation. Remaining residues were assembled using automated microwave-assisted SPPS. Cleavage was performed using TFA/TIPS/H2O (95:2.5:2.5 v/v) for 2 hours. Crude peptide, Figure S3A, was subjected to oxidative folding in GSH:GSSG 2 mM: 0.4 mM in 0.1 M NH4HCO3 (pH 8.5), containing 20% (v/v) isopropanol, Figure S3B. The peptide was purified using a Phenomenex Jupiter C18 column (250 × 10 mm, 5 µ) and a gradient from 5 to 97% AcN, in 0.05% TFA. The pure synthetic peptide was subsequently co-injected with the isolated peptide in the HPLC system, to confirm correct folding, Figure S3C.
NMR structure determination
Synthetic α-1 was dissolved in 90% H2O/10% D2O, and data were collected on a Bruker Avance 600 MHz spectrometer equipped with a cryoprobe. 2,2-Dimethyl-2-silapentane-5-sulphonate was used as internal standard (0.0 ppm). TOCSY, NOESY, 13CHSQC and 15NHSQC data were recorded at 298 K. TOCSY spectra were collected at 288–308 K with 5 K increments to establish temperature coefficients used for prediction of hydrogen bonds31. NMR spectra were assigned in CARA32. CYANA 3.033 was used to assign NOE data and translate NOE intensities into distance restraints, with the final structures being refined in explicit water using CNS34. The 50 structures with lowest overall energies were evaluated with MolProbity35, and the 20 models with best stereochemistry chosen to represent the solution structure of α-1. PDB ID: 6ENA. Atomic RMSD was calculated over the residues between the first and last cysteine residues using MOLMOL36, Table S2. The Dali server12 was used to identify structural homologues, regardless of sequence similarity, Fig. 4D.
Carcinus maenas Assay
Green crabs (20–50 g) were injected with control (500 µl sterile filtered sea water) or nemertide α-1 dissolved in sterile filtered sea water, into the cephalothorax between the first and second walking leg on the right side of the crab. Doses ranged from 0.1–50 µg/kg, in a maximal volume of 500 µl. The crabs were placed into a container filled with seawater and observed. All injections were made in duplicate.
Heterologous Expression in Xenopus laevis Oocytes
Complementary DNA encoding the NaV-channels was subcloned into the corresponding vector: the α-subunits rNaV1.1/pLCT1(NotI), rNaV1.4/pUI-2(NotI), hNaV1.5/pcDNA3.1(XbaI), mNaV1.6/pLCT(NotI), cockroach Blattella germanica BgNaV1.1/pGH19(NotI), Drosophila melanogaster DmNaV1, Varroa destructor VdNaV1, and the corresponding β-subunits rβ1/pSP64T(EcoRI) and Drosophila melanogaster TipE/pGH19(NotI). The linearized plasmids—respective restriction enzymes are indicated in parentheses—were transcribed using the T7 (for rNaV1.1, rNaV1.4, mNaV1.6, BgNaV1.1, TipE) or the SP6 (for hNaV1.5 and rβ1) mMESSAGE-mMACHINE transcription kit (Ambion, Austin, TX). The harvesting of stage V-VI oocytes from anaesthetized female Xenopus laevis frogs was described previously37. Oocytes were injected with 50–70 nl of cRNA at a concentration of 1–3 ng/nl using a micro-injector (Drummond Scientific, Broomall, PA). The oocytes were incubated in a ND96 solution containing: NaCl, 96 mM; KCl, 2 mM; CaCl2, 1.8 mM; MgCl2, 2 mM and HEPES, 5 mM (pH 7.4), supplemented with 50 mg/l gentamycin sulfate and 0.5 mM theophylline. Oocytes were stored for 1–5 days at 16 °C until sufficient expression of NaVs was achieved.
Whole-cell currents from oocytes were recorded at room temperature (18–22 °C) by the two-electrode voltage clamp technique using a GeneClamp 500 amplifier (Molecular Devices, Sunnyvale, CA) controlled by a pClamp data acquisition system (Molecular Devices). Oocytes were placed in a bath containing ND96 solution. Voltage and current electrodes were filled with 3 M KCl, and the resistances of both electrodes were kept between 0.7 and 1.5 MΩ). The elicited currents were sampled at 20 kHz and filtered at 2 kHz using a four-pole, low pass Bessel filter. To eliminate the effect of the voltage drop across the bath grounding electrode, the bath potential was actively controlled by a two-electrode bath clamp. Leak subtraction was performed using a-P/4 protocol. Whole-cell current traces were evoked every 5 s by a 100-ms depolarization to the voltage corresponding to the maximal activation of the NaV-subtype in control conditions, starting from a holding potential of −90 mV. Concentration-response curves were constructed by adding different toxin concentrations directly to the bath solution. The percentage of NaV modulation was plotted against the logarithm of the applied concentrations and fitted with the Hill equation: y = 100/[1 + (IC50/[toxin])h], where y is the amplitude of the toxin-induced effect, IC50 is the toxin concentration at half maximal efficacy, [toxin] is the toxin concentration and h is the Hill coefficient. To investigate the effects on the voltage dependence of activation, current traces were induced by 100-ms depolarizations from a holding potential of −90 to 65 mV with 5-mV increments. To investigate the effects on the steady-state inactivation process, oocytes were depolarized using a standard two-step protocol. From a holding potential of −90 mV, 100-ms prepulses were generated, ranging from −90 to 65 mV with 5-mV increments, immediately followed by a 100-ms test pulse to 0 mV. Data were normalized to the maximal Na+ current amplitude, plotted against prepulse potential and fitted using the Boltzmann equation: INa/Imax = [(1 - C)/(1 + exp((V - Vh)/k))] + C, where Imax is the maximal INa, Vh is the voltage corresponding to half-maximal inactivation, V is the test voltage, k is the slope factor, and C is a constant representing a non-inactivating persistent fraction (close to zero in control). Comparison of two sample means was made using a paired Student’s t test (p < 0.05). All data was analyzed using pClamp Clampfit 10.0 (Molecular Devices®, Downingtown, PA) and Origin 7.5 software (Originlab®, Northampton, MA) and is presented as mean ± standard error (S.E.M) of at least 3 independent experiments (n ≥ 3).
Lineus longissimus transcriptomic data is deposited in NCBI SRA: SRX1967959. Nemertide α−1 solution NMR structure is deposited in RCSB PDB: 6ENA.
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UG was supported by The Swedish Research Council (2014-3327). JT was supported by the following grants: G.0433.12 and GOE3414N (F.W.O. Vlaanderen), IUAP 7/10 (Inter-University Attraction Poles Program, Belgian State, Belgian Science Policy), OT/12/081 (KU Leuven). KJR is an Australian Research Council Future Fellow.
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