In vivo assembly and trafficking of olfactory Ionotropic Receptors
Ionotropic receptors (IRs) are a large, divergent subfamily of ionotropic glutamate receptors (iGluRs) that are expressed in diverse peripheral sensory neurons and function in olfaction, taste, hygrosensation and thermosensation. Analogous to the cell biological properties of their synaptic iGluR ancestors, IRs are thought to form heteromeric complexes that localise to the ciliated dendrites of sensory neurons. IR complexes are composed of selectively expressed ‘tuning’ receptors and one of two broadly expressed co-receptors (IR8a or IR25a). While the extracellular ligand-binding domain (LBD) of tuning IRs is likely to define the stimulus specificity of the complex, the role of this domain in co-receptors is unclear.
We identify a sequence in the co-receptor LBD, the ‘co-receptor extra loop’ (CREL), which is conserved across IR8a and IR25a orthologues but not present in either tuning IRs or iGluRs. The CREL contains a single predicted N-glycosylation site, which we show bears a sugar modification in recombinantly expressed IR8a. Using the Drosophila olfactory system as an in vivo model, we find that a transgenically encoded IR8a mutant in which the CREL cannot be N-glycosylated is impaired in localisation to cilia in some, though not all, populations of sensory neurons expressing different tuning IRs. This defect can be complemented by the presence of endogenous wild-type IR8a, indicating that IR complexes contain at least two IR8a subunits and that this post-translational modification is dispensable for protein folding or complex assembly. Analysis of the subcellular distribution of the mutant protein suggests that its absence from sensory cilia is due to a failure in exit from the endoplasmic reticulum. Protein modelling and in vivo analysis of tuning IR and co-receptor subunit interactions by a fluorescent protein fragment complementation assay reveal that the CREL N-glycosylation site is likely to be located on the external face of a heterotetrameric IR complex.
Our data reveal an important role for the IR co-receptor LBD in control of intracellular transport, provide novel insights into the stoichiometry and assembly of IR complexes and uncover an unexpected heterogeneity in the trafficking regulation of this sensory receptor family.
Ionotropic receptors (IRs) are a subfamily of ionotropic glutamate receptors (iGluRs) , an ancient class of ligand-gated ion channels present in animals, plants and prokaryotes [2, 3, 4]. Comparative genomics analyses suggest that IRs evolved in the last common ancestor of protostomes and probably derived from the AMPA/Kainate clade of iGluRs , which have well-characterised roles in synaptic transmission in animal nervous systems . In contrast to these iGluRs, IR repertoires have greatly expanded in size and display high sequence diversity within and between species . Moreover, transcriptomic and in situ investigations in a range of animals indicate that Ir genes are expressed in peripheral, rather than central, neurons [5, 6, 7, 8, 9]. Functional studies of IRs, in particular in Drosophila melanogaster, have shown that these receptors have diverse roles in environmental sensing, including in olfaction [6, 10, 11, 12], gustation [13, 14, 15, 16, 17, 18, 19, 20, 21], hygrosensation [22, 23, 24] and thermosensation [25, 26, 27].
While some progress has been made in defining the molecular basis of tuning IR response specificity [10, 11], the assembly and trafficking of IR complexes in vivo remain poorly understood. One intriguing unresolved question is the role of the co-receptor LBD. In heteromeric iGluR complexes, each subunit is thought to bind an extracellular ligand (typically glutamate or glycine) and to contribute to the gating of the ion channel pore [2, 3, 30]. It is unlikely that the IR co-receptors bind to the diversity of ligands that activate neurons in which they are expressed (which are presumed to be recognised by the LBD of the particular tuning IR in a given neuron type [10, 11, 28]). One possibility is that the IR co-receptor LBD interacts with a ligand present ubiquitously in the extracellular lymph fluid that bathes the ciliated outer dendritic segment of IR-expressing sensory neurons. The LBDs of both IR8a and IR25a retain most of the principal glutamate-contacting residues of iGluRs , raising the possibility that glutamate or a structurally related molecule is such a ligand. However, the observation that several of these residues are dispensable for the function of IR8a  implies that the co-receptor LBD has a role that is independent of ligand interactions.
IR co-receptor LBDs contain a distinctive N-glycosylated protein loop
To investigate the role of the IR co-receptor LBD, we first examined the sequence of this region for any unusual structural features. As in iGluRs, the LBD of IRs consists of a ‘Venus fly trap’-like structure formed by two lobes (S1 and S2), which are separated in the primary sequence by the ion channel domain (Fig. 1a). We generated a multiprotein sequence alignment of the predicted LBD of diverse D. melanogaster IRs, including the co-receptors IR8a and IR25a, various tuning IRs and selected mammalian iGluRs. This alignment revealed the presence of a stretch of ~ 30–35 amino acids near the beginning of the S2 domain in IR8a and IR25a that are not aligned to either tuning IR or iGluR sequences (Additional file 1: Figure S1). We termed this region the ‘co-receptor extra loop’ (CREL) (Fig. 1a). The CREL is highly conserved across orthologous co-receptors from diverse species (Fig. 1b and Additional file 2: Figure S2). Consistent with the overall relatedness of the co-receptors, the IR8a and IR25a CRELs share several characteristics, including the presence of predicted short alpha-helical and beta-sheet regions and a single consensus N-glycosylation target motif (NXS/T) (Fig. 1b and Additional file 2: Figure S2). Although the N-glycosylation site motif is conserved in all CREL sequences in IR8a and IR25a, its position varies by precisely four amino acids in a small subset of orthologues (Fig. 1b and Additional file 2: Figure S2). As this motif is located in a putative alpha-helical region, this displacement would be predicted to maintain the site on the same face of the helix.
We next sought to determine whether the CREL can be N-glycosylated. Because of the prohibitively limited quantities of protein we could obtain from tissues in vivo, we used HEK293 cells to express and purify recombinant IR8a LBD (corresponding to the termite Zootermopsis nevadensis sequence, which was the most promising candidate of several IR8a orthologues screened). We split the sample in two, treated one with peptide-N-glycosidase F (PNGase F), and subjected both to SDS-PAGE with in-gel tryptic digestion before analysis using liquid chromatography-tandem mass spectrometry (LC-MS/MS). When treated with PNGase F, N-linked glycans are removed from glycosylated asparagine residues, which become deamidated to aspartic acid (resulting in an increase in peptide mass by 1 mass unit) . Thus, an increase in the abundance of tryptic peptides containing aspartic acid following PNGase F treatment is indicative that these sequences originally contained a glycosylated asparagine. By contrast, such treatment does not affect peptides containing unmodified asparagine residues, whose abundance should therefore remain unchanged. For the IR8a LBD, we identified a tryptic peptide (m/z 648.29842+) whose peak intensity increased ~ 1000-fold after PNGase F treatment (Additional file 3: Figure S3). Subsequent analysis determined its sequence as DITLN*SSSDQSK (where N* refers to a deamidated asparagine residue), which corresponds to the predicted N-glycosylation site of the CREL (Additional file 3: Figure S3A and Fig. 1b). An adjacent tryptic peptide (m/z 676.32762+; sequence N*AEDVLYNVWK) had a similar abundance in the untreated and PNGase F-treated samples (Additional file 3: Figure S3B), indicating that this sequence is not N-glycosylated. These data indicate that the predicted CREL N-glycosylation site can bear a sugar modification.
The IR8a CREL N-glycosylation site has a selective role in regulating subcellular trafficking
To determine whether the CREL and the CREL N-glycosylation site are required for IR function in vivo, we focused on D. melanogaster IR8a, because the tuning receptor partners of this co-receptor (i.e. acid-sensing IRs in the antenna, the main olfactory organ of insects) are better understood than for IR25a [10, 11, 28, 32]. We generated transgenes encoding N-terminally EGFP-tagged mutant versions of IR8a bearing either a small deletion of the CREL (removing T658-D681) or a point mutant that disrupts the N-glycosylation site (N669Q), as well as a wild-type IR8a control. These transgenes (UAS-EGFP:Ir8awt, UAS-EGFP:Ir8a∆CREL and UAS-EGFP:Ir8aN669Q) were inserted at the same location in the D. melanogaster genome to eliminate any positional effects on their expression.
We first expressed these transgenes in olfactory sensory neurons (OSNs) under the control of the Ir8a-Gal4 driver . OSN dendrites are housed within cuticular sensilla that cover the external surface of the antenna as well as lining the sacculus, an internal multichambered pocket (Fig. 1c, d). We focused our attention initially on the subpopulation of IR8a-positive sacculus OSNs that co-express the tuning receptor IR64a , because the larger soma and dendrites of these neurons—compared to other IR8a-expressing OSNs that innervate coeloconic sensilla —facilitate observation of subcellular protein distribution (Fig. 1e).
As these neurons also express endogenous IR8a, we next expressed these transgenes in an Ir8a mutant background. As observed previously, EGFP:IR8awt localised normally while EGFP:IR8a∆CREL failed to be targeted to the sensory cilia and was destabilised (Fig. 2b). This protein instability appears to be a secondary consequence of the failure in localisation because examination of neurons in young (< 1 day old) animals did not reveal such a difference in protein levels, despite their absence from cilia (Additional file 4: Figure S4). Unexpectedly, in the absence of wild-type IR8a, EGFP:IR8aN669Q displayed much stronger defects in cilia localisation (Fig. 2b). These observations indicate that the presence of endogenous IR8a can complement the localisation defect of EGFP:IR8aN669Q. This result has two implications: first, that within cilia-localised IR complexes, there must be at least two IR8a subunits, providing in vivo evidence for the stoichiometry of IR complexes suggested by in vitro experiments . Second, the ability of EGFP:IR8aN669Qto localise to sensory cilia in the presence of IR8a indicates that this mutant protein is not defective in either folding or assembly into transport-competent IR complexes. Rather, the post-translational modification site in the CREL must have a selective effect on subcellular trafficking.
Heterogeneous requirement for the IR8a CREL N-glycosylation site in the localisation of tuning IRs
To examine the role of the IR8a CREL in trafficking of other tuning IRs, we surveyed the localisation of these three EGFP:IR8a fusion proteins in Ir8a neurons across the antenna. While EGFP:IR8a∆CREL was never detected in sensory cilia (in several hundred OSNs visualised), EGFP:IR8aN669Q could be observed in the endings of a subset of neurons innervating coeloconic sensilla, even in the absence of endogenous IR8a (Additional file 5: Figure S5A-B). We reasoned that this differential trafficking ability of IR8aN669Q might be related to the tuning IR with which it is co-expressed.
Our observation that wild-type IR8a can promote cilia transport of IR8aN669Q (Fig. 2a, b) raised the question of whether a tuning IR that is targeted to cilia with IR8aN669Q can facilitate the localisation of a tuning IR that cannot, if they are incorporated into a common complex. We tested this possibility in two ways: first, we examined the distribution of IR64a in its own neurons expressing EGFP:IR8aN669Q (but not endogenous IR8a) together with a control receptor (IR75a, which cannot localise to cilia with IR8aN669Q) or test receptors (IR75c or IR84a, which can localise with IR8aN669Q). While co-expression of IR75c or IR84a (but not IR75a) promoted cilia targeting of EGFP:IR8aN669Q, in no case did this lead to localisation of IR64a to the sensory compartment (Additional file 6: Figure S6A). Rather, the levels of IR64a were substantially reduced upon co-expression of an additional tuning IR. This might be because these ectopically expressed IRs preferentially combine with EGFP:IR8aN669Q, thereby excluding IR64a from associating with the co-receptor resulting in its destabilisation (as observed previously [28, 32]). Second, in Or22a neurons, we misexpressed IR75a together with EGFP:IR8awt or EGFP:IR8aN669Q, in the absence or presence of IR75c. Unexpectedly, we observed that addition of IR75c led to lower levels and abolished cilia localisation of IR75a when co-expressed with EGFP:IR8awt (Additional file 6: Figure S6B), suggesting that IR75c outcompetes—rather than collaborates—with IR75a to form stable, transport-competent complexes. Together, these results indicate that different tuning IRs do not readily assemble into a common complex with IR8a.
We next asked what molecular features might explain why some IRs can localise with EGFP:IR8aN669Q. IR75c and IR84a are not distinguished from IR64a and IR75a by phylogenetic relatedness  or any obvious sequence motifs (data not shown). Given that it is lack of an N-glycosylation site on IR8a that exposes distinct properties of these tuning receptors, we hypothesised that these IRs have complementary glycosylation sites. The LBD of IR84a contains three putative N-glycosylation motifs (N222, N272, N289) located on the predicted external surface of the domain (based upon comparison of their location with structures of the iGluR LBD (e.g. )). We generated a mutant version of IR84a in which all of these sites were mutated (mCherry:IR84aN222Q,N272Q,N289Q) and expressed this receptor (or an mCherry:IR84awt control) together with EGFP:IR8awt or EGFP:IR8aN669Q in Or22a neurons. Cilia localisation was observed in all cases (Additional file 7: Figure S7), suggesting that IR84a LBD glycosylation is not an essential compensating factor that permits localisation with IR8aN669Q.
IR8a CREL and the CREL N-glycosylation site are important for ER export
To determine where in the endomembrane system the trafficking of IR8a∆CREL and IR8aN669Q is blocked, we visualised the distribution of these EGFP-tagged receptors relative to markers for different organelles: endoplasmic reticulum (ER) (labelled with tdTomato:Sec61β ), Golgi apparatus (labelled with γCOP:mRFP ) and the cilia transition zone (labelled with antibodies against B9d1 ). We used genetically encoded markers for the ER and Golgi in order to express them only in the OSNs of interest, thereby avoiding confounding signal from the organelle-rich epidermal cells in the antenna .
IR8a CREL N-glycosylation is dispensable for the function of IR complexes
We extended this analysis with a second tuning receptor, IR75c, which detects propionic acid . Although Or22a neurons displayed weak endogenous responses to this odour, these are much lower than those exhibited upon expression of IR75c+EGFP:IR8awt (Fig. 5c, d). As expected, IR75c+EGFP:IR8a∆CREL-expressing neurons had similar propionic acid sensitivity to those lacking IRs (Fig. 5c, d). In contrast to the observations with IR84a, IR75c+EGFP:IR8aN669Q co-expression yielded responses that are decreased compared to IR75c+EGFP:IR8awt (Fig. 5c, d), which might reflect defects in function or diminished levels of cilia localisation not discernable with available reagents. Together, however, these observations indicate that the CREL glycosylation is not essential for IR signalling.
The IR8a CREL is likely to be exposed on an external face of an IR heterotetrameric complex
To obtain experimental evidence for the configuration of IRs in vivo, we used a protein fragment complementation assay with an enhanced yellow fluorescent protein (EYFP) reporter [42, 43]. Complementary and non-associating subfragments of EYFP (EYFP(1) and EYFP(2)) were fused to the N-termini of IR8a and IR84a, respectively, separated by short flexible linkers (Fig. 6c), and these proteins were expressed in Ir8a neurons singly or together. Neither fusion protein alone was fluorescent (Fig. 6d, e), but upon co-expression, we detected a robust EYFP signal in all Ir8a neurons (Fig. 6f), indicating direct association or close apposition of IR84a and IR8a. Similar results were obtained when EYFP fragment tags were exchanged on these receptors (Fig. 6g). EYFP fluorescence was detected both around the nucleus in the soma and in the ciliated dendritic endings, but not axons, indicating that the complex is likely to form in the endoplasmic reticulum (Fig. 6g, right).
In addition to analysis of these heteromeric interactions, we expressed together EYFP(1):IR8a and EYFP(2):IR8a. These fusion proteins also reconstituted EYFP fluorescence (Fig. 6h), suggesting the existence of homomeric interactions between two IR8a subunits. We also co-expressed EYFP(1):IR84a and EYFP(2):IR84a, but observed that these did not reconstitute a fluorescence signal (Fig. 6i). The simplest explanation for this result is that the EYFP fragments on IR84a subunits are not sufficiently close to each other in a tetrameric complex and/or are sterically inhibited from associating due to a ‘barrier’ of the interacting IR8a ATDs. Importantly, the result also provides a negative control that indicates that the EYFP reconstitution observed in the tagged IR84a+IR8a and IR8a+IR8a pairs is likely due to the formation of specific protein complexes, rather than simply their coexistence in the same neuronal membranes. Together, these observations are consistent with the model of an IR heterotetramer in which the ATDs of two IR8a subunits are directly apposed (Fig. 6a).
The characterisation of the IR8a CREL has revealed a critical role of an N-glycosylation site in the IR co-receptor LBD in regulating receptor transport from the ER to sensory cilia. This property is likely to be relevant for the functionally diverse IR8a- and IR25a-containing complexes in different sensory systems. Our data also provide insights into the stoichiometry and assembly of IR complexes in vivo, supporting a model in which two co-receptor subunits form a ‘core’—possibly interacting via their ATDs —with which two tuning IR subunits associate in the ER. Future structural analysis of IR8a (and other IRs) will be necessary to uncover the precise conformation of the CREL within IR complexes. Outside of this sequence, the IR8a LBD contains several additional predicted N-glycosylation sites; while their role (if any) is unknown, our data indicate that N-glycosylation of the CREL has a unique contribution to the regulation of IR trafficking.
The unexpected heterogeneity in the localisation properties of different IR complexes in which N-glycosylation of the CREL is prevented suggests that each tuning/co-receptor complex has a unique conformation that is assessed at a trafficking checkpoint in the ER: in some cases, the CREL N-glycosylation site is a key part of the signal permitting exit from this organelle, while in others it is dispensable. There are no obvious sequence motifs that can account for the distinction of these different types of IRs. We speculate that the observed heterogeneity is related to the conformational flexibility of the LBDs within an IR complex, as this is a property of iGluR LBDs that influences ER export , and tuning IR LBDs are highly diverse in sequence. These context-dependent trafficking properties in the IR family are reminiscent of the variable dependence of different mammalian odorant receptors on specific accessory proteins for ER exit . Such heterogeneity may reflect the ‘conflict’ that exists during the diversification of chemosensory receptor families, as individual members are under selective pressure both to maintain conserved cellular properties (i.e. trafficking to sensory cilia) and to evolve novel sensory-detection capacities.
Our data reveal an important role for the IR co-receptor LBD in control of intracellular transport, provide novel insights into the stoichiometry and assembly of IR complexes and uncover an unexpected heterogeneity in the trafficking regulation of this sensory receptor family.
Alignments were made with MUSCLE  and visualised in Jalview 2.9.0b2 . Secondary structure predictions were made using Quick2D . The IR8a homology model was built using SWISS-MODEL , with the R. norvegicus GluA2 structure (PDB: 6DLZ ) as template.
Deletions and point mutations in Ir8a and Ir84a coding sequences (lacking the region encoding the endogenous signal sequence, as described previously ) were introduced by standard PCR-based mutagenesis methods. Wild-type and mutant Ir8a sequences were subcloned into pUAST-EGFP attB, which encodes the calreticulin signal sequence fused to EGFP . Wild-type and mutant Ir84a sequences were subcloned into an equivalent pUAST-mCherry attB . Similarly, transgenes for EYFP protein fragment complementation were generated by joining sequences encoding EYFP(1) or EYFP(2) (with the calreticulin signal sequence)  to Ir8a or Ir84a sequences with an intervening short linker (encoding [GGGGS]2) in pUAST attB .
The sequence of ZnevIr8aS1S2 was synthesised by GENEWIZ and encodes the S1 domain (residues A366-P490) and the S2 domain (residues P608-N781) connected by a GTGT peptide. This sequence was cloned into a pcDNA vector for mammalian cell expression with a human IL2 signal sequence (MYRMQLLSCIALSLALVTNS), a 9xHis-tag and a Factor Xa cleavage site added to its N-terminus. The protein was expressed and secreted from FreeStyle HEK 293-F cells (Thermo Fisher) and purified directly from the cell culture medium using Ni2+-NTA resins. The protein was eluted from the resins with a high concentration of imidazole and further purified by a Superdex-200 size-exclusion column in a buffer containing 50 mM Tris, pH 8.0 and 400 mM NaCl.
Peptide sequencing by LC-MS/MS
Tryptic peptides were analysed by LC-MS/MS using an LTQ-Orbitrap XL MS (Thermo Fisher) coupled on-line with an Easy-nLC 1000 (Thermo Fisher) . Each MS/MS experiment consisted of one MS scan in FT mode (350–1800 m/z, resolution of 60,000 at m/z 400) followed by ten data-dependent MS/MS scans in IT mode with normalised collision energy at 29%. Protein identification and characterisation were performed by database searching using the Batch-Tag within the developmental version of Protein Prospector (v5.17.0)  against a targeted database consisting of ZnevIR8a sequences. The mass accuracies for parent ions and fragment ions were set as ± 20 ppm and 0.6 Da, respectively. Trypsin was set as the enzyme, and a maximum of two missed cleavages were allowed. Protein N-terminal acetylation, methionine oxidation, N-terminal conversion of glutamine to pyroglutamic acid and asparagine deamidation were set as variable modifications. Peptide relative abundances were evaluated based on extracted chromatograms of the selected ions during MS scans.
Flies were maintained on a standard corn flour, yeast and agar medium at 25 °C in 12-h light:12-h dark conditions. The wild-type strain was w1118. We used the following published D. melanogaster strains: Ir8a1 (RRID:BDSC_41744) , Ir8a-Gal4 (RRID:BDSC_41731) , Or22a-Gal4 (RRID:BDSC_9952) , UAS-Ir75a , UAS-Ir75c , UAS-Ir84a (RRID:BDSC_41740) , UAS-tdTomato:Sec61β (BSDC_64747)  and UAS-γCOP:mRFP (BDSC_29714) . New transgenic flies were generated by Genetic Services Inc. or BestGene Inc., via the phiC31 site-specific integration system, using the attP40 and attP2 landing site strains  for insertions on chromosomes 2 and 3, respectively. Genotypes are provided in the figure legends. Both sexes were used in most experiments except for some genotypes containing the Ir8a1 mutant allele (on the X chromosome), when only hemizygous males (Ir8a1/Y) were used; there is no known sexually dimorphic expression or function of IR8a.
Immunohistochemistry and imaging
The following primary antibodies were used: guinea pig anti-IR8a (1:1000) (RRID:AB_2566833) , rabbit anti-IR64a (1:1000) (RRID:AB_2566854) , rabbit anti-IR75a (1:1000) (RRID: AB_2631091) , rabbit anti-IR75c (1:200) (RRID: AB_2631094) , guinea pig anti-B9d1 (1:2500) , mouse monoclonal 21A6 (1:200) (RRID:AB_528449) (Developmental Studies Hybridoma Bank), mouse anti-GFP (1:1000) (Invitrogen A11120), anti-RFP (1:1000) (Abcam ab62341). Secondary antibodies: Alexa488 anti-mouse (1:1000) (Invitrogen A11029), Cy3 anti-guinea pig (1:1000) (Jackson Immunoresearch 106–166-003), Cy3 anti-rabbit (1:1000) (MILAN Analytica AG 111–165-144 0), Cy5 anti-guinea pig (1:1000) (Abcam ab102372).
Microscopy was performed using a Zeiss LSM 710 Inverted Laser Scanning Confocal Microscope. Confocal images were processed with Fiji .
For all experiments presented, images of antennal sections are representative of analysis of a minimum of 20 flies from at least two independent genetic crosses (samples sizes and number of replicates are provided in the corresponding figure legends). The phenotypes described are generally qualitative in nature (e.g. localisation or no localisation to cilia). It is very difficult to accurately quantify protein levels in cilia because the signals are inherently variable within a sample due, for example, to heterogeneous driver strength and the precise section cut, which can influence antibody permeation of the sensillar hair. Moreover, the cilia signals cannot be confidently normalised to the expression level in the corresponding soma, as these two parts of the neuron may not necessarily be in the same tissue section, and the dendritic region typically has a very weak signal, which leads to ambiguity in determining the soma corresponding to a given cilium.
Single sensillum extracellular recordings were performed and analysed essentially as described , using odour cartridges assembled as detailed in . Phenylacetic acid (CAS #103-82-2) and propionic acid (CAS #79-09-4) were from Sigma-Aldrich and were of the highest purity available. Odorants were used at 1% (v/v) in double-distilled H2O.
We acknowledge Benoîte Bargeton and Sabine Mentha for preliminary experiments and for generation of plasmid constructs. We thank Bénédicte Durand and the Developmental Studies Hybridoma Bank (NICHD of the NIH, University of Iowa) for antibodies, the Bloomington Drosophila Stock Center (NIH P40OD018537) for flies, and members of the Benton laboratory for comments on the manuscript.
L.L.P.-G. was supported by a FEBS Long-Term Fellowship. This work was supported by the University of Lausanne, ERC Starting Independent Researcher and Consolidator Grants (205202 and 615094) to R.B., an HFSP Young Investigator Award (RGY0073/2011) to R.B. and R.J., the SNSF Nano-Tera Envirobot project (20NA21_143082) to R.B., and the National Institutes of Health (R01GM074830) to L.H.
Availability of data and materials
All materials and data supporting the findings of this study are available from the corresponding author on request. Data from LC-MS/MS analyses are available at: ftp://MSV000083577@massive.ucsd.edu/ (password: CREL).
L.A. performed all experiments except for Additional file 3: Figure S3 (H.P., C.G., L.H. and R.J.) and Fig. 5 (L.L.P.-G.). R.B. generated sequence alignments, protein models and plasmid constructs. All authors contributed to experimental design, analysis and interpretation of results. R.B. directed the project and wrote the paper with input from other authors. All authors read and approved the final manuscript.
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