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First published online September 30, 2005; 10.1105/tpc.105.034678 © 2005 American Society of Plant Biologists
A Continent of Plant Defense Peptide Diversity: Cyclotides in Australian Hybanthus (Violaceae)
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONRESULTSDISCUSSIONMETHODSREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMETHODSREFERENCES |
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; Craik, 2001; Göransson et al., 2003; Gustafson et al., 2004; Trabi and Craik, 2004). They are characterized by their head-to-tail cyclization and cystine knot motif (Craik et al., 2001), which contribute to their exceptional resistance to physical, chemical, and biochemical degradation (Gran, 1973a; Colgrave and Craik, 2004). Topologically related macrocyclic peptides containing a cyclic cystine knot also occur in a plant from the Cucurbitaceae family (Hernandez et al., 2000; Felizmenio-Quimio et al., 2001), and a range of other circular proteins have been discovered in bacteria, plants, and animals over recent years (Trabi and Craik, 2002; Craik et al., 2003). The cyclotides display antiviral, uterotonic, and other biological activities (Gran, 1973b; Gustafson et al., 1994; Witherup et al., 1994; Tam et al., 1999; Craik, 2001) but are believed to function in vivo as insecticidal agents (Jennings et al., 2001). The mechanism by which they act is currently under investigation but is believed to be mediated through disruption of biological membranes (Nourse et al., 2004; Kamimori et al., 2005). Because of their great stability and well-defined molecular architecture, the cyclotides have attracted attention as potential frameworks for peptide-based drug design (Craik et al., 2002).
At present, 
50 cyclotide sequences and nine three-dimensional structures have been reported (Saether et al., 1995; Daly et al., 1999; Skjeldal et al., 2002; Rosengren et al., 2003; Barry et al., 2004; Trabi and Craik, 2004; Chen et al., 2005; Jennings et al., 2005; Koltay et al., 2005; Mulvenna et al., 2005). Structures of linear analogues (Barry et al., 2003) and a disulfide-deficient mutant (Daly et al., 2003) are also available. Figure 1 shows a selection of cyclotide sequences from a range of genera together with a typical three-dimensional structure. The sequences are aligned based on the six conserved Cys residues and show that certain backbone loops between Cys residues are highly conserved. Also shown are sequence logos (Crooks et al., 2004) to graphically depict current knowledge of cyclotide sequences. Preliminary analysis of available plant material has shown a wealth of sequence diversity within the cyclotides, indicating that thousands of unique sequences may exist (Trabi and Craik, 2004). This diversity represents a significant potential resource for the development of environmentally friendly crop protection agents that might avoid the development of resistance by target insects (Craik et al., 2004). However, contrary observations, such as the presence of near-identical cyclotide sequences in widely diverged species such as Oldenlandia affinis (Rubiaceae) and Viola arvensis (Violaceae), as shown in Figure 1, call into question the potential range of variation of this class.
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; Göransson et al., 2003; Svangård et al., 2003, 2004; Trabi and Craik, 2004) despite the many other genera in the Violaceae. To address these deficiencies, an extensive examination of cyclotide diversity in wild populations of Australian Hybanthus (Violaceae) was conducted in order to gauge the level of cyclotide diversity within populations, within currently defined species across their geographical distributions, and between species. It was hoped that this information would shed light on the cyclotide variation of individual Hybanthus populations and the potential utility of cyclotide profiles as a chemotaxonomic feature in the Violaceae. Furthermore, knowledge of sequence diversity will assist in the utilization of the cyclotide framework as a protein engineering tool.
More generally, the number of reported antimicrobial and defense peptides has increased significantly in the last few years, with >700 sequences being sourced from organisms ranging from bacteria to plants and animals. In plants, although investigations into variations in small secondary metabolites, such as alkaloids and terpenes, in wild populations have been reported (Turner, 1967; Da Costa et al., 2005), even in Viola itself (Flamini et al., 2003), similar studies for peptide variation in wild populations are lacking. Among the few examples of studies of peptide variation, the diversity of Bowman-Birk protease inhibitors in cultivated lentils and their wild relatives (Sonnante et al., 2005) has been examined, as has the chemotaxonomic utility of antimicrobial peptides in frogs (Apponyi et al., 2004). In contrast with most peptides, the unusual stability, high levels of expression, and hydrophobicity of cyclotides permit straightforward isolation and characterization, making them ideal candidates for evaluating peptide diversity in nature. In this study, cyclotides in Hybanthus from across the Australian continent were sampled to evaluate the diversity of this peptide family and, more broadly, to give insights into the diversity of peptides in nature. A new approach to the identification of cyclotide sequences was developed, and insights into the role of different amino acids at specific locations in the structure were derived.
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RESULTS |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMETHODSREFERENCES |
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, and another two species were sampled from dried herbarium specimens. With the exception of H. floribundus (subsp floribundus (eastern) and subsp adpressus) and H. enneaspermus, plants were typically observed to form small isolated colonies of three to five plants, limiting the breadth of sampling. To minimize ecological impact, root material was not collected, although previous studies have clearly established that cyclotides are present in roots of Violaceae species (Trabi and Craik, 2004). Collection localities are summarized in Figure 2, with the total distribution of each species (adapted from Bennett, 1972) shown in gray or black (first and second listed species per map, respectively), with letters indicating the position of each population collected within its geographical range. Specimens obtained from dried material are indicated with an asterisk.
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A similar pattern is found in the more diverse H. monopetalus in Figure 5. In comparison with H. calycinus, this species has fewer common peptides between sites, consistent with its greater morphological and ecological variation and the greater separation of populations. Once again, the number of unique peptides in each population was observed to increase with decreasing latitude (4, 3, and 18 peptides from populations C, B, and A, respectively).
The cyclotides of H. epacroides and H. bilobus, two species with an unusual spiny growth habit, were investigated, as the separation of these species is contentious (Bennett, 1972). The dried herbaria specimens of H. bilobus were found to give reliable LC-MS traces. The clustering of a mass from a dried herbarium sample of H. floribundus subsp chloroxanthus with other H. floribundus subspecies collected from live material indicated that the cyclotides were unchanged by preservation and storage. The analysis of H. epacroides and H. bilobus suggested only limited affinity between the two forms through a single clustered peak.
The less thoroughly sampled species studied showed comparable patterns. For H. aurantiacus, there was little overlap between northern and central populations, with only a single set of coincident peptides in Figure 5. H. stellarioides contained a single cyclotide in the limited sample studied, but as fruiting material was not available, further diversity may exist. The profiles for H. vernonii subsp vernonii were found to be very consistent between northern and southern populations despite marked morphological and ecological differences (from montane sandstone to coastal scrub, respectively).
Across all species, the distribution of masses and retention times both followed approximately bell curve distributions as shown in Figure 6. Compounds were observed to vary in mass from 2800 to 3800 D and in retention time from 10 to 20 min. The average mass was slightly skewed lower than the midpoint of the range of masses, and the average retention times appear roughly grouped into two sets. Overall, the new data significantly expanded the range of masses seen previously for cyclotides.
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). Hyfl A is similar to the previously reported cyclotides circulin A and Hypa A (68 and 74% identity, respectively). By contrast, Hyfl B and C both contain amino acid substitutions previously unseen in cyclotides, namely a Gln and Met in loop 6, Lys in loop 2, and tandem Glu residues in loop 3 (see Figure 1 for the definitions and locations of the backbone loops in cyclotides). Interestingly, the Met residue in Hyfl B was found in the oxidized state only, while both oxidized and unmodified forms were found in Hyfl C. The presence of the tripeptide sequence AET in loop 1 is also novel. Previously reported cyclotides have the sequences GES, GET, or AES in this highly conserved loop.
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; Dutton et al., 2004), 16 additional partial cyclotide sequences were determined, as shown in Table 1. A further seven complete cyclotide domain sequences (Hyfl D-E and Hyfl I-M) were determined using a forward primer annealing to a newly identified conserved element within the endoplasmic reticulum (ER) signal of previously characterized cyclotide precursors from the Violaceae family (Dutton et al., 2004; Mulvenna et al., 2005). The strategy used for obtaining these sequences is outlined in Figure 7 and is based on knowledge of the generic cyclotide precursor structure, which comprises regions coding for an ER signal sequence, a propeptide domain, the mature peptide domain, and a small hydrophobic tail C-terminal to the mature domain. A region within the propeptide sequence just upstream of the mature domain is referred to as the N-terminal repeat (NTR) region, as some cyclotide precursors have up to three tandem copies of it and an adjacent mature cyclotide domain.
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) and V. tricolor (Mulvenna et al., 2005) showed a high degree of sequence similarity (see Supplemental Table 2 online), pointing to a vital role of this domain in the processing of precursors to produce mature cyclotides. Secondary structure prediction identified a helical motif in the NTR region that is conserved in other known cyclotide precursors and is believed to play a role in folding, processing, or detoxification of cyclotide domains from the precursor (Dutton et al., 2004). |
DISCUSSION |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMETHODSREFERENCES |
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Isolation and analysis of the peptides from one Hybanthus species by MS-MS sequencing characterized three novel cyclotides, namely Hyfl A-C. Comparison of Hyfl A with the previously determined sequence of Hypa A from the Argentine H. parviflorus (Broussalis et al., 2001) indicates high sequence similarity. The other two new peptides displayed residues previously unseen in their respective loops. These peptides demonstrate that nontrivial variations in cyclotide sequence remain to be discovered and highlight the importance of continuing investigations into other genera in the Violaceae. The expanding diversity of sequences also increases the likelihood that different cyclotides will possess different activities in vivo. The observed diversity demonstrates the versatility of the cyclic cystine knot as a combinatorial template, reinforcing the suggestion that it has exciting potential applications in drug design (Craik et al., 2002). Of the 54 published cyclotide sequences, only two contain Met residues. Two more Met-containing cyclotides are presented in this study (Hyfl B and C), and in both cases oxidized forms of Met were detected. This result is consistent with a previous study (Chen et al., 2005), where an oxidized Met residue was reported to be very solvent exposed, accounting for 7.5% of the total surface area of the cyclotide.
We have previously isolated partial cDNA clones from O. affinis (Jennings et al., 2001), V. odorata (Dutton et al., 2004), and V. tricolor (Mulvenna et al., 2005) by RT-PCR using forward primers based on known cyclotide sequences. The partial cDNA clones were sequenced and used either directly to screen a cDNA library (Jennings et al., 2001; Dutton et al., 2004) or for design of gene-specific primers to screen a rapid amplification of cDNA ends library (Mulvenna et al., 2005) for full-length clones. In this study, we have used a similar approach to amplify partial cDNA clones from Hybanthus but without subsequent cDNA or rapid amplification of cDNA ends library construction to obtain the full-length clones. Although this strategy allows for rapid assessment of the diversity within mature cyclotide domains, the first three to four amino acids of this domain fall outside the primer region and are therefore not detected. This prevents comparison of predicted mass for the cDNA isolated peptide sequences with peptide masses found by LC-MS analysis of plant extracts.
In a new approach, we therefore designed a forward primer that targets a newly identified conserved element (AAFALPA) in the precursor sequence upstream of the mature cyclotide domain, identified by comparison of previously isolated full-length cyclotide precursors in the Violaceae family (Dutton et al., 2004; Mulvenna et al., 2005). Figure 7 shows the architecture of typical cyclotide precursors and highlights the previously unreported conserved sequence element in the ER signal domain. Using primers targeted to this region and to oligo(dT) in RT-PCR proved successful for obtaining the full sequence of the mature domain as well as most of the precursor without the need for cDNA library construction and screening. Also, using a primer that binds upstream of the mature domain sequence rather than to known sequences within the cyclotide itself increases the likelihood of isolating cyclotides with hitherto unseen sequences. Cyclotides with rare sequences that are less abundant in the plant may be an indication of increased biological activity, as the plant would need smaller amounts of a more active peptide.
There are two main subfamilies of cyclotides, termed Möbius and bracelet. Members of the Möbius subfamily are characterized by a conserved cis-Pro in loop 5 that creates a twist in the cyclic backbone, thereby making it conceptually similar to a Möbius strip. Bracelet cyclotides do not have the cis-Pro and, consequently, have no twist in the backbone. Moreover, in Möbius cyclotides discovered to date, there is practically no variation in loop sizes, and the net charge is generally neutral or negative, whereas known bracelet cyclotides have variable loop sizes and commonly carry a net charge of +2. Approximately two-thirds of the cyclotides reported to date belong to the bracelet subfamily. Most of the cyclotide sequences isolated from the Hybanthus spp in this study lack the cis-Pro in loop 5 and are classified as bracelet peptides, except for Hyca A and Hymo B, which are assigned to the Möbius subfamily.
Many of the new cyclotides contain sequence elements not previously observed. For example, Hyca A has an unusual loop 2 of five residues (VVDTR) as opposed to the standard four in Möbius cyclotides. Also, the amino acid content of this loop stands out, and the hydrophobic patch partially formed by this loop is most likely expanded due to the presence of two successive hydrophobic residues. With two consecutive Lys residues in loop 4, not found in any other cyclotides to date, Hyca A has a net charge of +2 and is thus more cationic than other Möbius cyclotides. Together with the increased hydrophobic region, this makes Hyca A more amphipathic. The unusual presence of a Met residue in loop 6 as seen in Hyfl B and C is also observed in Hyca A.
Solution structures of the bracelet cyclotides circulin A (Daly et al., 1999) and cycloviolacin O1 (Craik et al., 1999; Rosengren et al., 2003), and the Möbius cyclotides kalata B1 (Rosengren et al., 2003) and kalata B2 (Jennings et al., 2005), show that the typical bracelet structure, with six to seven residues in loop 3, features a short helical segment in this region, whereas in Möbius cyclotides, the four residues in loop 3 form a type II ß-turn. Interestingly, the new bracelet cyclotides Hyen B, Hyep A, and Hyfl E, F, J, G, and M have a short loop 3 of only four residues, suggesting that this region forms a turn, as in Möbius cyclotides, rather than a helix. Furthermore, in Hyen B, Hyfl F/J, and Hyst A, the conserved Pro preceding Cys III in bracelets is substituted with other residues, and all but one (Hyen B) of these bracelet cyclotides with a shortened loop 3 have a Pro in position 3 of this loop, as do most Möbius cyclotides. Both Pro residues are important for the turn geometry in the respective subfamilies (Rosengren et al., 2003), further strengthening the suggestion that the bracelet cyclotides mentioned above feature a loop 3 typical of Möbius cyclotides. Hyfl F was also interesting due to an expanded loop 5 of six residues (NHHDKV) as opposed to the usual four in bracelets, showing that the cyclotide framework is capable of tolerating a range of sequences of varying length and amino acid content. This finding is very significant, as it suggests that loops 3 and 5 are potentially amenable to the grafting of foreign bioactive epitopes into the sequence in protein engineering or drug design applications (Craik et al., 2002).
In other so far known cyclotides, the one-residue loop 4 consists of a Ser, a Lys, or a Thr, but in Hyfl E, Hymo B, and Hyst A, a Tyr, an Ala, and a His, respectively, form this loop. Other unusual amino acid combinations of the newly discovered cyclotide sequences include KVTKR, IWGR, and TTFN in loop 2 of Hyen B, Hyst A, and Hyfl F and GFGI/ KNRG in loop 5 of Hyst A and Hyve A, respectively. Hyve A further lacks the conserved Asn or Asp in loop 6 thought to be involved in cyclization, raising the question whether this peptide might be an acyclic homologue.
Finally, it is interesting to note the substitution of the conserved Gly residue preceding Cys IV with a Lys in Hyca A and Asn in Hyfl E and Hyfl F. Only in three cyclotides reported to date is this residue not a Gly, namely, an Asn in circulin D and circulin E (Gustafson et al., 2000) and a Glu in Vodo M (Svangård et al., 2003). It is thought that a positive 
angle in the peptide backbone of the last residue in this loop is important for defining the type II ß-turn that is needed to link loop 3 to the cystine knot (Rosengren et al., 2003). Gly residues readily adopt conformations with positive angles due to the absence of a side chain. Asn also has the ability to adopt positive angles by forming a stabilizing hydrogen bond between the side chain and main chain, thereby introducing a turn in the backbone. Most other amino acids cannot adopt this conformation due to steric hindrance by the side chain. However, Lys residues are also known to be capable of adopting positive angles. The substitution of the Gly with a Lys in Hyca A will therefore probably allow for turn geometry consistent with other cyclotides.
The experimental methods developed to measure cyclotide diversity in this study proved effective on minimal amounts of wild collected material (<200 mg) and gave reproducible resolution to within 1 D and 1 min retention time by LC-MS. Only three masses comparable to those of cyclotides occurred outside of the 10- to 20-min retention time band, and very few peptide masses inconsistent with cyclotides (<2000 or >4000 D) occurred in this band. This suggests that cyclotides are present at relatively high concentration in plant tissue and possess distinct mass and chromatographic properties, rendering their isolation and analysis straightforward and reliable. Although it is possible that some cyclotides may have been missed by the extraction and LC-MS procedure, the gradient used covered a wide range of hydrophilic/hydrophobic properties, and we are confident that the vast majority of cyclotides present was detected. Cyclotide diversity within an individual species varied from a single peptide (H. stellarioides) to 32 peptides (H. enneaspermus). The extremes of variation seen in these two species are noteworthy, considering they were once classified as a single taxon (Bennett, 1972). On average, 10 to 20 cyclotides were seen per species. Considering there are 900 species (Ballard et al., 1999) in the Violaceae (for which every species investigated to date has contained cyclotides), it is conservatively estimated that there are >9000 unique cyclotides in this plant family.
The variation seen between individual plants in a population is possibly attributable to variations in cyclotide expression rather than differences in genetics given previous observations showing the dependence of cyclotide profile on plant tissue and season (Trabi and Craik, 2004; Trabi et al., 2004). In the well-sampled population of H. enneaspermus (Figure 5), tissues were separated for one plant and indicated increasing cyclotide diversity from leaves to flowers to fruits (3, 4, and 13 different cyclotides, respectively). This is consistent with cyclotides serving as defense molecules and is comparable to the localization of specific plant defensins to the stigma of Nicotiana (Atkinson et al., 1993; Nielsen et al., 1995) in that the most critical tissues for plant reproduction are the most heavily protected. The pattern of increasing incidence of unique cyclotides with decreasing latitude in H. calycinus and H. monopetalus may be a reflection of greater numbers or diversity of pathogens and herbivores in warmer climates.
The influence of geographical isolation of Hybanthus populations is seen in the cyclotide profiles of H. floribundus and its subspecies in Figure 4. This species has been described as consisting of a type form (subsp floribundus) present in southeastern and southwestern Australia and several additional morphologically distinct forms in the southwest (subsp adpressus, chloroxanthus, curvifolius, and "Hill River"). The Nullarbor desert represents a genetic barrier that separates the Hybanthus populations of these two regions. Analysis of the cyclotide profiles of this group reveals a tendency for western collections of all subspecies to cluster more highly together than to the eastern population. This suggests that the eastern and western populations of the type subspecies are at least as distinct as the described morphological variants in the southwest and that H. floribundus subsp floribundus could be further split to account for this difference.
The data generated in this study allow some conclusions about taxonomic relationships between Hybanthus species to be derived. A comparison of the cyclotide physicochemical data across all species (see Supplemental Figure 1 online) using similar criteria for collating peptides within species revealed 42 peptides that could be shared between species. In Figure 8, each species is represented as an oval or a rectangle (Hybanthus section Variabiles, E.M. Bennett, or Suffruticosi, G.K. Schulze, respectively; Bennett, 1972). This analysis demonstrated a network of relationships through possible common peptides. The western Australian subspecies of H. floribundus clustered closely together and displayed well-defined links to H. epacroides, H. cymulosus, H. monopetalus, and H. vernonii. Connections between H. monopetalus and H. aurantiacus, and H. aurantiacus and H. enneaspermus were also seen. The latter relatively isolated grouping is noteworthy, as these species are the section Suffruticosi of Hybanthus (along with H. stellarioides that displayed only a single peptide with uncertain relationships), although all other Australian species are in section Variabiles (Bennett, 1972). Continuing work on cDNA isolation from the collected samples is expected to provide a clearer picture of the evolution of the Australian Hybanthus and their cyclotides.
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This study adds to the emerging picture of the diversity of defense peptides throughout all major phyla in nature. Initiatives in collating this emerging information have been made for knottins (Gelly et al., 2004) and antimicrobial peptides (Tossi and Sandri, 2002; Brahmachary et al., 2004; Wang and Wang, 2004) in the form of online databases of the expanding list of cDNA and peptide sequences and their structures and activities. A database of cyclotide sequences (www.cyclotide.com) will soon be substantially updated to accommodate this rapidly growing family.
In conclusion, this study indicates that an extensive range of cyclotides remains to be identified in natural populations of plants in the Violaceae. The estimated >9000 unique cyclotides in this plant family represents an enormous wealth of peptide diversity for potential use in crop protection, based on the insecticidal activity of the prototypic cyclotides kalata B1 (Jennings et al., 2001) and B2 (Jennings et al., 2005). The novel sequences indicate that nontrivial variations on cyclotide sequences await discovery. The pattern of cyclotides potentially common to multiple species of Australian Hybanthus corresponded with previously described relationships derived from morphological features. The low impact of field collection and the simplicity of measuring cyclotide LC-MS profiles indicate that they provide a convenient chemotaxonomic feature to assist the classification of the Violaceae.
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Extraction
Samples, including flowering or fruiting material (20 to 50 mg) where available, were frozen in liquid nitrogen and ground to a fine powder and then extracted overnight into 2 mL of methanol:dichloromethane (50:50). Next, 1 mL of water was added and the aqueous layer collected and then another 1 mL of methanol was added for overnight extraction. The extract was similarly diluted with 1 mL of water and separated the following day. The resulting methanolic aqueous extract was freeze-dried and subjected to reverse-phase chromatography on a Strata-X 33-µM polymeric sorbent column (30 mg/mL; Phenomenex). Samples were loaded in 1 mL of 20% acetonitrile/water with 0.1% formic acid to a preequilibrated column, washed with 1 mL of the same solution, then eluted with 1 mL of 90% acetonitrile with 0.1% formic acid and freeze-dried to give a cyclotide-enriched fraction.
LC-MS Analysis
Peptide samples were dissolved in 50 µL of 25% acetonitrile/water with 0.1% formic acid. Analysis was performed on an HP Series 1100 LC/auto-injector coupled to a Micromass LCT mass spectrometer (Waters) equipped with an electrospray ionization source. Samples of 25 µL were subjected to a gradient of 90% acetonitrile with 0.1% formic acid over 0.1% aqueous formic acid (25 to 75% over 30 min at 0.3 mL/min) on a Grom column (150 x 2 mm, 3 µm, equipped with a security guard column, flow rate 300 µL/min). Mass spectra were acquired over a mass range of 800 to 1800 D with a capillary voltage of 3.5 kV and a cone voltage of 30 V. Data were analyzed and processed using MassLynx software.
MS-MS Sequencing
The 150 g sample of H. floribundus subsp floribundus was homogenized and extracted into dichloromethane:methanol following published procedures (Trabi et al., 2004). Individual peptides were isolated through repeated reverse-phase HPLC using gradients of 90% acetonitrile:10% water:0.5% trifluoroacetic acid against 100% water:0.5% trifluoroacetic acid. Purified cyclotides were reduced at a ratio of 6 nmol of peptide in 20 µL of 0.1 M NH4HCO3, pH 8.0, to 1 µL of 0.1 M Tris-carboxyethylphosphine at 65°C for 10 min. The reduction was confirmed by matrix-assisted laser desorption ionization time of flight MS after desalting using ZipTip purification (Millipore), which involved several washing steps followed by elution in 10 µL of 80% acetonitrile (0.5% formic acid). The desalted samples were mixed in a 1:1 ratio with matrix consisting of a saturated solution of 
-cyano-4-hydroxycinnamic acid in 50% acetonitrile (0.5% formic acid). Two hundred shots per spectrum were acquired in positive ion reflector mode on a Voyager DE-STR mass spectrometer (Applied Biosystems). The laser intensity was 1800, the accelerating voltage was 20,000 V, the grid voltage was 64% of the accelerating voltage, and the delay time was 165 ns. The low mass gate was 500 D. Data were collected between 500 and 5000 D. Calibration was undertaken using a peptide mixture obtained from Sigma-Aldrich (MSCal1). The mixture contained bradykinin, angiotensin, and insulin B chain.
Enzymatic Digestion and Nanospray MS-MS Sequencing
To the reduced peptide, trypsin, endoGlu-C, or both was added to give a final peptide-to-enzyme ratio of 50:1. Trypsin and endoGlu-C digestions were performed for 1 and 3 h, respectively, while in the combined digestion, initial trypsin incubation for 1 h was followed by addition of endoGlu-C for a further 3 h. The digestions were quenched by the addition of an equal volume of 0.5% formic acid and desalted using ZipTip technology (Millipore). Samples were stored at 4°C prior to analysis. The digestion products were examined by matrix-assisted laser desorption ionization time of flight MS followed by sequencing by nanospray MS-MS on a QStar mass spectrometer (Chen et al., 2005). A capillary voltage of 900 V was applied, and spectra were acquired between mass-to-charge ratios of 60 to 2000 for both time of flight spectra and product ion spectra. The collision energy for peptide fragmentation was varied between 10 and 50 V, depending on the size and charge of the ion. The Analyst QS software program was used for data acquisition and processing. The MS-MS spectra were examined and sequenced based on the presence of both b- and y-series of ions present (N- and C-terminal fragments). Chymotrypsin digests using the same conditions as for trypsin were also conducted to confirm the results obtained for each of the peptide sequences. Amino acid composition was confirmed by amino acid analysis. The disulfide connectivity of CysI-IV, CysII-V, and CysIII-VI was assumed based on homology with previously reported cyclotides (Göransson and Craik, 2003).
RNA Extraction, RT-PCR, and Secondary Structure Prediction
Plant material stored in RNAlater solution was subjected to mRNA isolation using the RNAqueous kit (Ambion). Single-stranded cDNA was prepared from RNA using the OneStep RT-PCR kit (Qiagen), which also facilitated amplification of partial clones by oligo(dT) and degenerate forward primers (Proligo) designed from known cyclotide or cyclotide precursor sequences. The primers used were as follows: 5'-GGGCHGCHTTYGCHCTTCCHGC-3', coding for the peptide sequence AAFALPA; 5'-CTNGGNAGYATHTCNTGYGG-3' (peptide sequence GSISC); 5'-GGGGATCCTGYGCNGARACNTG-3' (peptide sequence CAETC); 5'-CGATCGATTGYGGIGARAGTTGYGT-3' (peptide sequence CGESCV); 5'-GGGGATCCTGYGGIGARACITG-3' (peptide sequence CGETC); and 5'-CGATCGATTGYGTITGGATHCCITG-3' (peptide sequence CVWIPC). The resulting DNA fragments were excised from agarose gel and cloned into the pCR 2.1-TOPO vector using the TOPO Cloning technology (Invitrogen) for sequencing. The amino acid sequences corresponding to the NTR of identified precursors were analyzed for secondary structure using the PROFsec program at the PredictProtein server (Rost et al., 2004) at http://www.predictprotein.org.
Accession Numbers
Sequence data from this article can be found in the UniProt Knowledgebase under accession numbers P84647 to P84649 (Hyfl A to Hyfl C, respectively) and in the GenBank/EMBL data libraries under accession numbers DQ192575 to DQ192577 (Hyfl D to Hyfl F, respectively) and DQ187926 to DQ187945 (Hyfl G to Hyep B, as listed in Table 1).
Supplemental Data
The following materials are available in the online version of this article.
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Acknowledgments |
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Footnotes |
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The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: David J. Craik (d.craik{at}imb.uq.edu.au).
Online version contains Web-only data.
Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.105.034678.
Received June 2, 2005; Revision received August 3, 2005. accepted September 1, 2005.
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REFERENCES |
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TOPABSTRACTINTRODUCTIONRESULTSDISCUSSIONMETHODSREFERENCES |
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