Introduction

‘Macromolecular refinement against high-resolution data is never finished, only abandoned’1. George Sheldrick’s statement on the labour-intensive nature of model building and refining crystal structures reflects the difficulty in producing highly accurate models. As a result, 85% of deposited protein crystal structures contain discernable errors2. Unfortunately, as crystal structures are frequently used as the basis of further studies, inaccurate crystal structures can cause significant harm to the scientific process. Continued improvement of crystal structure accuracy therefore remains an important goal within the biology community.

Recently, in a class assignment, we asked 57 undergraduate students to build the structure of a protein, lectin scytovirin3, using only the model-building program Coot and an electron density map downloaded from the electron density server4. Students were not given the amino-acid sequence of the protein, but were provided with the position of the N-terminal amino acid. The students were instructed to build the structure of the protein, residue by residue, into the 2FoFc electron density map. Many students expressed appreciation for the puzzle-like quality of the assignment. In addition to learning about protein structure, 10% of these students improved on the previously published model4. One student even generated a structure that ranked in the 100th percentile in both Molprobity clashscore and total score when compared with other structures in its resolution range. These results raised the intriguing possibility that even a relatively small group of amateur model builders could collectively build higher-quality models than a single trained crystallographer. This concept was remarkably reminiscent of ideas recently championed by the online protein-folding computer game Foldit5.

On the basis of the success of the undergraduate students in improving a published crystal structure, we hypothesized that crystallographic model building through crowdsourcing might result in more accurate crystal structures than those resulting from traditional model-building methods. Thus, we added electron density features to Foldit to allow players to build directly into density. We then administered a competition to determine if crowdsourcing crystal structures could lead to top-notch structural models. The competition showed that Foldit players could build very high-quality crystal structures into electron density maps, opening up a new method for building and refining crystal structures. In addition, solving the structure of the competition’s test protein unexpectedly led to the discovery a new family of histidine triad (HIT) proteins potentially involved in preventing amyloid fibre formation.

Results

Adding electron density to Foldit

Foldit is a popular video game that crowdsources protein structure prediction5, challenging players to discover low-energy protein models by exploring protein conformational space. The newest version of Foldit provides players with electron density maps and the associated protein sequences, and asks players to use experimental data to guide protein folding (Fig. 1; Supplementary Fig. 1). With these new features, players can trim maps around a model and customize features of the electron density map, such as contour level, rendering style and transparency (Supplementary Fig. 1). The standard Foldit score function is supplemented with a fit-to-density term, allowing in-game structure minimization similar to crystallographic real-space refinement6. Foldit players are able to view the fit-to-density score for each residue of a model, providing valuable feedback about specific parts of a model that require more attention. As a preliminary test of this feature, we gave an electron density puzzle to the Foldit players that was nearly identical to the lectin scytovirin classroom assignment mentioned above, and found that the Foldit players were also able to improve on the published scytovirin structure (Supplementary Note 1; Supplementary Fig. 2).

Figure 1: Snapshots of Foldit players building YPL067C in the Foldit user interface.
figure 1

For the complete path of the Foldit model building, see Supplementary Movie 1. The starting point for the puzzle (top left) presented the electron density map and the protein sequence to the player. The players then used Trp108 to help anchor the sequence in electron density (top middle) before beginning to fold secondary structure elements (top right through bottom left). After many rounds of modification in Foldit (bottom middle and Supplementary Movie 1), the players arrived at a high-scoring solution in which the ordered regions of electron density were well fit by YPL067C (bottom right). Disordered regions were later pruned.

The model-building competition

We then held a crystallographic model-building competition to compare the effectiveness of different model-building approaches. Five groups of competitors took part in our model-building competition: (1) 469 Foldit players worldwide, (2) two trained crystallographers, (3) 61 undergraduate students in the University of Michigan class MCDB411 (Introduction to Protein Structure and Function) who built the structure as a class assignment, (4) Phenix Autosolve7,8 and (5) MR-Rosetta9. We chose YPL067C, a yeast protein with no significant sequence similarity to any structure in the Protein Data Bank (PDB) (Supplementary Note 2) as the target for our competition. In addition, YPL067C was chosen for its biological interest, as previous studies suggested that YPL067C is involved in preventing amyloid toxicity10. Crystals of this protein diffracted to 1.9 Å resolution (Table 1). We asked all human competitors to build the best possible protein structure that they could given the protein sequence, a secondary structure prediction and an experimentally phased, density refined map of YPL067C. The MCDB411 class assignment was conducted similarly to the previous crystallography assignment discussed above, in which undergraduates improved on a published crystal structure4. As before, the undergraduates lacked previous model-building experience. In contrast, 54% of the participating Foldit players had attempted to solve early electron density puzzles in Foldit and thus had some experience in Foldit-based model building. Both the trained crystallographers and undergraduates used the model-building and real-space refinement program Coot11, whereas the Foldit players used the Foldit version released on 14 October 2015. None of the competitors were given any starting points for building, and thus they needed to establish the relationship between the electron density and the protein’s sequence.

Table 1 Crystallography statistics for HTC1.

The various groups used different approaches. The students and trained crystallographers worked independently, generally utilizing large aromatic residues to identify the relationship between sequence and electron density features. The best Foldit solutions, in contrast, came from a group of players working collaboratively, with one player serving as the trailblazer who contributed the majority of the moves towards the creation of the model (Fig. 1), and other players providing detailed structural tweaks and refinements (Supplementary Movie 1). Although the Foldit players also used a large aromatic residue to initially anchor the sequence similar to the Coot users, their building process sampled conformational space very widely (Supplementary Movie 1), unlike the Coot users. The Foldit players used many different types of building tools, including constraint changes (band, freeze and cut actions), automated minimization algorithms (global wiggle, local wiggle and shake actions) and tools to modify secondary structure (rebuild and tweak actions) (Supplementary Fig. 3).

To determine which group produced the best structural models, we used an automated refinement procedure12 on all the structures, and then compared key crystallographic statistics. These statistics consisted of Rfree, r.m.s.d.’s of bonds and angles, the number and severity of steric clashes (represented by Molprobity clashscore13), and Ramachandran outliers. Analysing the Rfree values, we quickly realized that the Foldit players were at a distinct disadvantage (Supplementary Fig. 4). Whereas the Coot users, Phenix Autosolve and MR-Rosetta were able to exclude regions that had poor quality electron density, the current version of Foldit required that players model the entire sequence without gaps, retaining all disordered residues. Because disordered atoms do not substantially contribute to X-ray diffraction, modelling of disordered residues will disagree with diffraction data and inflate Rfree values. To correct for this deficiency in Foldit, we pruned the Foldit models afterwards to include only those residues modelled by the top trained crystallographer, so that they contained only the well-ordered regions of the protein. We then re-refined the pruned Foldit structures and compared them with the other models.

The Foldit structures improved considerably after pruning. As a result, the top pruned Foldit structure was the overall highest-quality structure produced in the competition (Fig. 2) as measured by geometry, density fit and steric clashes. In addition to the Rfree value of the pruned Foldit structure becoming marginally better than that achieved by the trained crystallographers and containing zero Ramachandran outliers, the Foldit structure had the lowest level of steric clashes (Fig. 2). According to Molprobity13, the top Foldit structure is an exceptional model, ranking in the 100th percentile in both its overall Molprobity score and clashscore of all structures in the PDB of similar resolution (1.95±0.25 Å). The superiority of the top Foldit structure can be attributed to better side-chain conformations than those in the top structure produced by the trained crystallographers (Supplementary Fig. 5). Better Foldit scores were associated with lower Rfree values (Supplementary Fig. 6), suggesting that the Foldit model-building strategy and its scoring algorithm could be generalizable as a means of producing high-quality structures.

Figure 2: Model-building competition results.
figure 2

Comparison of key statistics of the best model from each group after pruning disordered residues from Foldit structures. In all cases, lower values represent better scores. Comparison before pruning disordered residues is shown in Supplementary Fig. 4.

Discussion

Here we show that Foldit players can build structural models at least as effectively as trained crystallographers and state-of-the-art automated methods, enabling a novel crowd-powered strategy for solving high-accuracy crystal structures. Combined with the ability to generate molecular replacement solutions in Foldit, and therefore to circumvent the need for experimental phases in some cases14, it is now potentially possible to obtain complete structure solutions using Foldit given only a native crystallography data set. Citizens hold a tremendous reserve of brainpower that remains largely untapped by the scientific community. The new Foldit electron density feature has revealed that non-expert citizen scientists are capable of using structural data to build first-rate models, and we expect that Foldit will be a powerful tool for crowdsourcing many new high-quality structures.

This surprising win by Foldit players suggests that, in at least some cases, this video game can help produce crystallographic models of higher quality than those from trained crystallographers or automated model-building algorithms alone. The difference in accuracy is likely in part the result of different underlying philosophies behind Coot and Foldit. Whereas Coot primarily uses a real-space refinement system15 that only respects local geometry, the Rosetta force field used by Foldit is much more extensive, including additional steric, electrostatic and solvation terms, as well as statistical potentials based on observed backbone torsions and side-chain rotamers6. That some of the Foldit models were of higher quality than those of trained crystallographers suggests that expert model builders might also benefit from the Foldit force field for real-space refinement. Human intervention either by crystallographers or Foldit players is clearly helpful, as both Phenix Autosolve and MR-Rosetta on their own produced suboptimal structures. The collaborative building process used by the Foldit players could also be a beneficial strategy for professional crystallographers, who could achieve a similar effect by either having multiple laboratory members take turns working on model building and refinement or by submitting their crystal refinement problems to Foldit. Looking forward, we hope that further analysis of electron density puzzle solutions in Foldit can inform continued improvement of automated structure solution algorithms.

Foldit players might also be tasked with improving structures of questionable quality already in the PDB. These Foldit puzzles would benefit the entire community of scientists that depend on accurate structural models. Editing of nearly complete structures could form a base of easier Foldit puzzles for new players, allowing players to practice their model-building skills before moving to more difficult de novo model-building puzzles. To further improve the capability for Foldit players to aid crystallographers, ongoing development will make it possible for the players to add or remove residues with insufficient electron density, and have these changes accurately reflected in the Foldit score. We envision a future in which professional crystallographers frequently tap the collective model-building expertise of Foldit players for help in the model-building, refinement and validation steps of crystallography.

From an educational perspective, the participation of an undergraduate class in this study explored how crystallographic model building can be used not just to teach students the structures and chemistry of proteins in great depth, but in addition, to teach the scientific process. In our previous study, students built into a high-resolution, fully refined map3. In the study presented here, students received a lower-resolution, unrefined map and no starting place for building. Dealing with disordered residues, the students were forced to interpret data of varying quality and to decide when the data became too ambiguous to draw firm conclusions. Similar decision-making processes govern the use of scientific data across many disciplines. This assignment thus helped give students a realistic view about the power and limitations of the scientific method. Importantly, the ease with which students and Foldit players were able to interpret and understand density maps suggests that scientists other than crystallographers can very readily interpret electron density maps, which will assist them in designing or analysing experiments based on crystal structures.

YPL067C’s structure yielded unexpected insights into its biological function. Despite the lack of sequence homology to any protein in the PDB, a DALI16 search of YPL067C (Supplementary Table 1) found that it is structurally similar to members of the widely conserved superfamily of histidine triad (HIT) proteins. These proteins contain three histidine residues with an almost identical spatial organization to that of YPL067C, as well as a ß-sheet core nested inside a similar arrangement of loops and helices (Fig. 3). HIT proteins have been shown to be involved in diverse cellular stress responses, such as DNA damage, oxidative stress and induced apoptosis17,18. However, the specific in vivo activity of HIT proteins remains unclear17. Although YPL067C bears some resemblance to known HIT proteins, it is sequentially and structurally distinct (Supplementary Fig. 7). Its most notable distinguishing structural characteristic is an open channel not found in other HIT proteins (Supplementary Note 2). YPL067C’s characterization makes it the founding member of a new family we are calling HTC (for histidine triad with channel), with YPL067C being the first member, HTC1. The HTC family contains over 900 members found in a wide variety of eukaryotes and viruses (Supplementary Note 2). As mentioned above, HTC1 null mutants increase the toxicity of amyloid overproduction10. We find here that HTC1 is very effective in preventing in vitro amyloid formation of three model proteins, Aβ1–40, α-synuclein and reduced carboxy-methylated α-lactalbumin (RCMalA; Fig. 4). On the basis of docking simulations, HTC1 may bind to unfolded proteins using its conserved channel (Supplementary Note 2; Supplementary Fig. 8). Our crowdsourcing-enabled discovery of a new family of proteins involved in preventing amyloid formation provides insight into a novel physiological role of the ubiquitous HIT proteins.

Figure 3: Overall structure of HTC1.
figure 3

Structural alignment with the top DALI search hit is shown in Supplementary Fig. 7.

Figure 4: HTC1 aggregation inhibition.
figure 4

HTC1 prevents amyloid formation of RCMLa (a) Aβ1–40 (b) and α-synuclein (c), as measured by thioflavin T (ThT) fluorescence at 490 nm.

Methods

Electron density in Foldit

To facilitate work on electron density data in Foldit, new visualizations and tools, along with a tutorial puzzle to introduce them, were developed and distributed to Foldit players in periodic software updates. Electron density maps in Foldit are displayed as a visual guide in the form of an isosurface. Players have control over parameters of the density isosurface, such as the contour level, surface texture, transparency and colour, and can tag regions of the density with notes. After initial testing, it was clear that density visualization alone was insufficient to improve model building by Foldit players. Players simply ignored the density, finding that their existing, familiar strategies were most competitive on Foldit leaderboards. In response, we adapted the Rosetta fit-to-density score term elec_dens_fast into the Foldit score function6. This not only provides competitive incentive to match the density, but also allows Foldit automated tools such as structure minimization to be guided by electron density, similar to crystallographic real-space refinement. Under this configuration, players were able to fit models to several experimental electron density maps with high accuracy. An important feature was added later that allowed players to trim excess density that was distant from the player’s model from the visualization. According to Foldit player testimony, this feature has proved invaluable on certain experimental density maps where it allowed a clearer interpretation of relevant density. To protect the integrity of unpublished crystallographic work, electron density data were obfuscated before online distribution to Foldit players.

The competition

Phenix Autosolve7,8, with model-building disabled, was used to create density-modified maps of selenenomethionine (SeMet) YPL067C. To make the map manageable for the Foldit program, the map was masked beyond 5 Å from the initial solution at the start of the competition. This map was given to Foldit players, MCDB411 students and the experienced crystallographers for model building. The individual responsible for model building and refining the initial structure solution of YPL067C, before the contest was initiated, had no contact with any of the competitors.

Sixty-one students in the University of Michigan undergraduate class MCDB411 (Introduction to Protein Structure and Function) were introduced to the assignment through a description of the previous iteration of the assignment in class4, together with a 1.5 h lecture on X-ray crystallography. Students then had two in-class computer laboratory sessions in which features of Coot were presented. In the first 1.5 h lab session, the students were given basic instructions on opening electron density maps and molecules, changing map levels, scrolling and changing map size, finding secondary structure elements, converting Cα representations to all-atom molecules, placing helices and strands, adding terminal residues, real-space refinement, controlling regularization and refinement, rotating and translating atoms and residues, viewing the skeleton, mutating residues, and changing rotamers. The instructors suggested that changing the weighting of the real-space refinement from the default value of 60–10 and making subsequent changes to this value as needed could help in the building process. In the second 1.5 h lab session, the students were taught how to merge molecules, look for grouped tryptophans, phenylalanines and/or tyrosines as starting places for building, and use validation tools such as density fit analysis, geometry fit analysis and unmodelled blobs. Four instructors were present in the first lab session and three in the second to answer questions on the operation of Coot. Starting from the initial lab session, students were given a total of 1 month to complete the assignment. During this period, the instructor held walk-in help sessions twice a week for 1.5 h each and answered questions on the operation of Coot as well as general model-building questions. Common questions included how to identify density for specific sequences, how to correctly merge molecules and how to approach gaps in electron density. Regarding gaps in density, students were told to model through gaps only if they were confident that the modelling would be correct based on the size of the gap and the number of residues they were modelling in. Students were not told what to do in specific cases of building through disordered segments. They were informed that water molecules would not be included in grading. One student asked whether there were external validation tools that could help and was told that the Molprobity server might be useful. Students were allowed to discuss the project and ask each other questions, but were required to do their own model building.

A Foldit puzzle was posted online with the masked electron density map and a model of the target polypeptide in fully extended conformation. Players were challenged to fold the extended polypeptide into the electron density map to achieve a good fit to density. Any advice given to MCDB411 students by the instructors as to how to begin model building was also posted on the Foldit messaging board. After 4 weeks, the puzzle was closed and 900,000-player models were scored and ranked according to the Rosetta energy function. The top scoring models were clustered into a set of 1,000 such that no two aligned to <1.0 Å Cα r.m.s.d. To this clustered set, we added the 50 best unique models produced by Foldit teams or soloists, as well as any models flagged by Foldit players for special consideration—1,094 Foldit models in total. The puzzle was open to Foldit players for 28 days. Members of the winning team began playing the day after the puzzle opened, and produced the winning structure 23 days later—4 days before the puzzle closed.

Two trained crystallographers were given the same number of days for model building as the students and Foldit players. They were given specific instructions not to use tools outside of Coot or Molprobity and not to interact with each other during model building. The trained crystallographers spent 8 and 14 h, respectively, working on the puzzle. The trained crystallographers reported using the following approach to the puzzle, which corresponds well with what the instructor observed with many of the undergraduate students. First, they looked for large density blobs that might correspond to large aromatic side chains such as Trp, Tyr or Phe. Working forwards and backwards from the Trp–Phe–Val–Asn sequence proved particularly useful. Modelling in a few of these large residues led to the assignment of density to sequence location. The direction of the polypeptide chain was reversed on a few occasions, but was fixed by looking at the carbonyl density. The Find Secondary Structure tool in Coot was used, especially for regions where the density was poor. Real Space Refine Zone was used with the refinement weight set to 20 or 10, based on the instructor’s suggestion for building in an unrefined map. Regions where the density was very poor and decisions had to be made about whether to keep trying to build or not proved to be the hardest part of the task. The trained crystallographers reported that at first they did build in these sections of poor electron density. However, when they realized the extent of the guessing involved, they subsequently removed most of the model in these areas. After modelling in the residues, the trained crystallographers used the validation tools in Coot, including Ramachandran plot, Rotamer analysis and Density Fit analysis, which flagged areas with poor geometry. They also ran the structure through MolProbity, which gave similar results to the Coot validation tools. Finally, the crystallographers fixed problem areas as best as possible with the Coot modelling tools, such as Flip Peptide, Rotamers, Regularize Zone and Real Space Refine Zone. When asked to describe the difficulty level of this assignment, the trained crystallographers rated it as somewhat difficult (on a scale of: very difficult, somewhat difficult, neither easy nor difficult, somewhat easy and very easy).

Phenix Autosolve7,8 was run with default parameters (using phase_and_build) to produce the Autosolve model. The MR-Rosetta model was obtained by relaxing and rebuilding the Autosolve model in the same electron density map provided to human groups, using Rosetta mr_protocols9 with nstruct=10 and selecting the model with the lowest Rfree. ARP/Warp19 and Phenix Autobuild20 did not create models of as high quality as Phenix Autosolve or MR-Rosetta, and were thus not analysed in the competition.

After completion of the competition, all structures were automatically refined using Phenix to analyse the results. The refinement strategy included XYZ coordinates, temperature factors and updating waters. Notably, the best structures from Foldit, as measured by Rfree, came from the group of highest-scoring Foldit structures according to Foldit score.

Bioinformatics

YPL067C sequence conservation was analysed using a four-iteration PSI-BLAST of the UniRef50 database, with an E-value cutoff of 0.005. No sequences in the PDB were found. Sequence conservation was projected onto the structure of YPL067C using the Consurf server21. The top DALI16 match to the crystal structure of YPL067C was to a HIT protein of unknown function from Clostridium difficile (PDB: 4EGU), with a Z-score of 4.9. The top 47 hits were all HIT proteins with Z-scores ranging from 4.9 to 4.2 (Z-scores >2.0 are considered significant). Secondary structure predictions for the competition were generated using PSIPRED22.

Protein expression and purification

The gene for YPL067C was amplified from yeast strain Y2HGold (Clontech) and cloned into a pET28-sumo plasmid using primer 1 (5′- AAATATGGATCCATGCAACAAGATATCGTCAACGATCACCAG -3′) and primer 2 (5′- AAATATCTCGAGTCAGGCAAGTGGCTCGAAACC -3′). pET28-sumo-ypl067C was transformed into Escherichia coli BL21(DE3) cells.

Cells were grown at 37 °C overnight in 100 ml Luria Broth (containing 100 μg ml−1 kanamycin), and 10 ml was used to inoculate 1 litre Luria Broth (containing 100 μg ml−1 kanamycin). At early log phase, the temperature was reduced to 20 °C and 0.1 mM isopropyl β-D-1-thiogalactopyranoside was added to induce expression overnight. Cells were collected by centrifugation and resuspended in 100 ml lysis buffer (40 mM Tris, 10 mM sodium phosphate, 400 mM NaCl, 10% glycerol, 10 mM imidazole, pH 8.0) enriched with 1 mg ml−1 DNaseI, 1 mM MgCl2 and two tablets of complete EDTA-free protease inhibitor (Roche). Cells were lysed by two French press cycles at 1,300 p.s.i. and centrifuged at 37,000 g for 30 min at 4 °C. The supernatant was run through a Ni-HisTrap 5 ml column (GE Healthcare) pre-equilibrated with lysis buffer at a rate of 1.5 ml min−1. Following binding, the column was washed with 60 ml lysis buffer. The protein was eluted with 20 ml lysis buffer enriched with 500 mM imidazole. To cleave the sumo-His × 6 tag, 10 μl ULP1 protease (from stock of 50 mg ml−1) was added to the eluted solution. A volume of 10 μl β-mercaptoethanol was added and the solution was dialysed overnight in 40 mM Tris, 10 mM sodium phosphate, 400 mM NaCl, 10% glycerol, pH 8.0. To remove the tag, the solution was run through a Ni-HisTrap 5 ml column (GE Healthcare) pre-equilibrated with dialysis buffer at a rate of 1.5 ml min−1, and the flowthrough was saved and diluted in eight volumes of 20 mM Tris, pH 8.0. The protein was then run through a HiTrap Q HP 5 ml column (GE Healthcare), and the flowthrough contained >95% pure YPL067C as measured by SDS–polyacrylamide gel electrophoresis. Before each experiment, YPL067C was exchanged into appropriate buffer. Expression and purification of SeMet YPL067C was performed with the same protocol except a methionine auxotroph variant of E. coli BL21(DE3) and SelenoMethionine Medium Complete (Molecular Dimensions) were used.

α-Synuclein was expressed and purified using the protocol described previously23 with minor modifications. In brief, 1% of the overnight grown culture was transferred in fresh media and induced with 0.8 mM isopropyl β-D-1-thiogalactopyranoside for 4 h after the optical density of the culture reached 0.6. The induced cells were pelleted at 4,000 r.p.m. and resuspended in 25 ml lysis buffer (10 mM Tris, 1 mM EDTA, pH 8). The lysed cells were then boiled at 95 °C for 15–20 min and centrifuged at 11,000 r.p.m. for 20 min. The supernatant was thoroughly mixed with 10% streptomycin sulfate (136 μl ml−1) and glacial acetic acid (228 μl ml−1) then centrifuged at 11,000 r.p.m. for 30 min. To the clear supernatant, an equal volume of saturated ammonium sulfate was added, and the solution was incubated at 4 °C for 1 h with intermittent mixing. The precipitated protein was separated by centrifugation at 11,000 r.p.m. for 30 min. The pellet was dissolved in equal volumes of absolute ethanol (chilled) and 100 mM ammonium acetate. Finally, the pellet was washed (twice; optional) with absolute ethanol, dried at room temperature and resuspended in 10 mM Tris, pH 7.4. The protein solution was filtered through a 50 kDa cutoff column (AMICON, Millipore) followed by ion-exchange chromatography (Q-sepharose) against a NaCl gradient. The fractions of pure protein eluted at 300 mM NaCl were checked on SDS–polyacrylamide gel electrophoresis and the molecular weight was confirmed by mass spectrometry. The pure fractions were pooled and dialysed overnight against buffer (10 mM Tris and 50 mM NaCl, pH 7.4). The concentration of α-synuclein was determined using ɛ280=5,600 M−1 cm−1. The purified α-synuclein was stored at −80 °C at a concentration of 100 μM until use.

1–40 peptide was purchased from AlexoTech AB (Umeå, Sweden) and prepared as previously described24. Aβ1–40 peptide was dissolved in 10 mM NaOH to a peptide concentration of 1 mg ml−1 and then sonicated for 1 min in an ice bath before dilution in the assay buffer. The preparations were kept on ice. α-Lactalbumin (aLA) from bovine milk (cat: L6010) and porcine citrate synthase (cat: C3260-5KU) were purchased from Sigma Inc. RCMaLA was prepared as previously described25. aLA (500 μM; freshly prepared in water) was incubated with 1 mM dithiothreitol in 0.5 M Tris and 1 mM EDTA, pH 7.0, for 10 min, then 3 mM iodoacetic acid (out of 1 M stock solution in water) was added and the solution incubated for another 30 min. aLA was then dialysed into 50 mM phosphate buffer, pH 7.0, 100 mM KCl, 10 mM MgCl2.

Protein crystallization

Native and SeMet YPL067C crystals were grown at 20 °C by vapour diffusion using both sitting (1 μl drops) and hanging drop methods (2 μl drops). Drops were prepared by mixing a 1:1 solution of YPL067C (25 mg ml−1) and reservoir solution (5.6–8.1% glycerol, 1.6–2.1 M ammonium sulfate and 0.1–0.2 M Tris). Crystals were cryoprotected by gradually supplementing the drop with glycerol up to 25% and were flash-frozen in liquid nitrogen.

X-ray crystallography

Data were collected at the Life Sciences Collaborative Access Team (LS-CAT) beamlines at the Argonne National Laboratory’s Advanced Photon Source at 100 K. The data were integrated and scaled using HKL2000. Phases and initial model building of the SeMet derivative were obtained using Phenix AutoSolve7,8. Native YPL067C was solved by molecular replacement with the initial SeMet structure. Iterative refinement and model building were performed using Phenix Refine12 and Coot11. Channel size was analysed using the 3V server26. Data collection and modelling statistics are shown in Table 1, and a section of the structure in its 2mFo-DFc map shown in Supplementary Fig. 10.

Fibrillar aggregation assays

Fibrillar aggregation was monitored by a thioflavine T (ThT) fluorescence assay. ThT is a benzothiazole dye that exhibits enhanced fluorescence specifically on binding to amyloid fibrils. For RCMaLA aggregation experiments, solutions containing 100 μM RCMaLA, YPL067C in varying concentrations and 20 μM ThT were prepared in 50 mM potassium phosphate buffer, pH 7.0, 100 mM KCl and 10 mM MgCl2 (ref. 25). The ThT fluorescence assays with Aβ1–40 peptide were performed with 2.5 μM Aβ1–40 peptide, YPL067C in varying concentrations and 20 μM ThT in PBS, pH 7.4, 1% dimethylsulphoxide. The fibrillar aggregation of α-synuclein was tested in a solution of 70 μM α-synuclein, YPL067C in desired concentrations and 20 μM ThT in PBS, pH 7.4. For α-syuclein assays, four glass beads were added in each well to induce aggregation.

ThT fluorescence assays were performed with a final volume of 100 μl of the prepared solution in black 96-microwell plates (costar, UV Plate, 96 well) that were sealed to prevent evaporation. ThT fluorescence was measured in a Synergy HT Multi-Mode Microplate Reader (Biotek) at 37 °C, with constant medium shaking. Excitation and emission wavelengths were 440 and 490 nm, respectively. All samples were assayed in triplicate and the assay was repeated twice. Incubation of YPL067C with ThT alone produced no fluorescence increase.

Docking of α-synuclein and HTC1

HTC1 was docked against a 200-member NMR ensemble of α-synuclein27 using ZDOCK 3.0.2 (ref. 28). The top five scoring poses of HTC1 bound to each member of the ensemble were used to generate a contact frequency map of the HTC1:α-synuclein interaction. To determine the contact map, an interaction was assigned to a given residue pair if their Cα–Cα distance was less than or equal to , where λ=1.2 and are taken from the mean Cα–Cα distance for residue pairs that form intermolecular contacts in the PDB29. For each intermolecular residue pair, we reported the contact probability averaged over the extracted binding poses. To project the contact maps onto the structures of α-synuclein and HTC1 on the same scale, the contact frequency for each residue pair was averaged over all residues.

Analytical ultracentrifugation

Sedimentation velocity experiments of HTC1 (Supplementary Fig. 9) were performed using a Beckman ProteomeLab XL-I analytical ultracentrifuge (Beckman Coulter). YPL067C was first dialysed against 20 mM HEPES, pH 7.5, then diluted to a concentration of 20 or 200 μM using the dialysis buffer. Samples were loaded into cells containing standard sector shaped two-channel Epon-centerpieces with 1.2 cm path length (Beckman Coulter) and equilibrated to 22 °C in the centrifuge for at least 1 h before sedimentation. All samples were spun at 48,000 r.p.m. in a Beckman AN-50 Ti rotor (167431.7 g at the centre of the cell), and the sedimentation of the protein was monitored continuously using the interference optics. Data analysis was conducted with SEDFIT (version 14.1)30, using the continuous c(s) distribution model. The confidence level for the ME (maximum entropy) regularization was set to 0.7. Buffer density and viscosity were calculated using SEDNTERP (http://sednterp.unh.edu/).

Data availability

The final model of HTC1 is deposited in the PDB under the code 5KCI. Other models and raw data are available on request.

Additional information

How to cite this article: Horowitz, S. et al. Determining crystal structures through crowdsourcing and coursework. Nat. Commun. 7:12549 doi: 10.1038/ncomms12549 (2016).