Building de novo cryo-electron microscopy structures collaboratively with citizen scientists

Abstract

With the rapid improvement of cryo-electron microscopy (cryo-EM) resolution, new computational tools are needed to assist and improve upon atomic model building and refinement options. This communication demonstrates that microscopists can now collaborate with the players of the computer game Foldit to generate high-quality de novo structural models. This development could greatly speed the generation of excellent cryo-EM structures when used in addition to current methods.

This Community Page article demonstrates that microscopists can now collaborate with the players of the computer game Foldit to generate thorough high-quality de novo structural models; this development could greatly speed the generation of excellent Cryo-EM structures when used as a complement to current methods.

Main text

Less than a decade ago, before the “resolution revolution,” cryo-electron microscopy (cryo-EM) was indulgently called “blobology” [1–4]. Whereas seminal work of cryo-EM experts resulted in high-resolution 3D maps and atomic models of ordered assemblies such as 2D crystals, helical arrays, and icosahedral viruses [5–11], commonly obtained 3D maps of less regular or asymmetric objects could be interpreted only in terms of global 3D architecture, domain organization, and—at most—secondary structure elements. Atomic model building was the privilege and expertise of crystallographers, requiring careful consideration of structural details such as bond geometry, steric clashes, and hydrogen bonds. Now, however, thanks to spectacular progress in both hardware and software, cryo-EM scientists suddenly face the necessity of building atomic models into near-atomic resolution maps. This unanticipated promotion from “blobologists” to “structure solvers” [12] is not as straightforward as it may seem, because model building and refinement are labor-intensive and require expertise in macromolecular structure. Spurred on by the improved resolution of newly obtained maps, the growing cryo-EM community has generated hundreds of excellent—but also some error-containing and energetically unfavorable—atomic models [1,13,14]. Such errors not only jeopardize the cryo-EM field itself but also misguide downstream research that relies on accurate molecular models, such as mutational analysis and structure-based drug design.

Although rigorous structure and model validation tools tailored for cryo-EM are currently under intense development [14,15], improving the quality of cryo-EM model building remains an important area of research. The recent introduction of computational model-building tools geared toward cryo-EM offer the possibility of automated model building [16–19]. However, building accurate models into near-atomic resolution cryo-EM maps remains a substantial challenge, because atom positions at this resolution are not unambiguous and must be inferred with aid from molecular mechanics models.

Citizen scientists have been able to contribute to challenging problems in fields such as RNA design [20], neuroscience [21], sequence alignment [22], and quantum physics [23]. Thus, one possible model-building option is Foldit (https://fold.it), a citizen science computer game that challenges players to solve complex biochemistry puzzles [24]. Recent improvements to Foldit enable players to build protein structures into crystallographic, high-resolution maps more accurately than expert crystallographers or automated model-building algorithms [25]. Unlike crystallographic maps, which often rely on phase data inferred from model coordinates, cryo-EM maps are more suitable targets for Foldit because averaged EM data are directly interpretable and are independent of the model. Here, we show that crowd-powered model building by Foldit players can indeed substantially help cryo-EM scientists.

To assess the usefulness of Foldit for cryo-EM, the players were provided with cryo-EM densities corresponding to 4 segmented subunits of the antefeeding prophage (AFP, from a soil bacterium Serratia entomophila)—Afp1, Afp5, Afp7, and Afp9 [34]. For ease of comparison, the maps were filtered to 3.2-Å resolution to avoid local quality variation and contain information up to the same resolution of 3.2 Å, which is currently considered fairly high by the cryo-EM community but still arduously low for fully automated model-building algorithms. The players tried to achieve the highest possible Foldit score, which combines the Rosetta force field with map fitting [26,27]. The structures generated by players were compared with those produced by a cryo-EM expert who created models using the manual model-building and real-space refinement software Coot [28], followed by additional real-space refinement in Phenix [29]. Structures generated by the state-of-the-art automated model-building algorithms Rosetta “denovo_density,” Phenix Map-to-Model, ARP/wARP, and Buccaneer [16–19] were included in the comparison. Standard EM validation tools and crystallographic statistics were used to evaluate the 4 approaches.

Table 1 compares the results of the various methods, using multiple criteria to evaluate both the model fit to the map and physical plausibility. Rosetta, Phenix, and Buccaneer struggled to correctly place certain chains in the appropriate density (Fig 1, S1–S11 Figs). This difficulty likely stems from errors in side-chain assignment, because the map resolution is often too poor for unambiguous side-chain identification, and these approaches fit regions of the map with incorrect sequences (Fig 1). All 4 automated methods had difficulty generating plausible geometry (Table 1, S1 Text). The Foldit structures and those generated by the microscopist produced accurate structures that were geometrically plausible and fit the maps well. Examining the models more closely shows that in most cases, the Foldit players placed slightly greater importance on bond geometry and steric clashes than the microscopist, who sacrificed these aspects for better fitting to the map (Table 1, Fig 1, S1 Text, S1 Table, and S1–S3 Figs). Although close in quality, at this resolution, we suggest it is appropriate to prioritize model geometry over map fit (Fig 1D–1G). Indeed, above 3-Å resolution, outliers are unlikely to be sufficiently supported by experimental data [14].

Table 1. Validation scores for all models.

Protein	Model	CCmask	CCbox	CCpeaks	CCvolume	FSC Average	Molprobity Score	Clash Score	Rama. Favored (%)	Rama. Allowed (%)	Rama. Outliers (%)	CaBLAM Outliers	RMSD B Length (Å)	RSMD Angles (°)
Afp1	Foldit	0.9	0.64	0.67	0.89	0.51	0.5	0	98.64	1.36	0	0.69	0.008	0.684
	Microscopist	0.93	0.68	0.72	0.91	0.53	1.52	3.52	94.52	4.11	1.37	2.78	0.008	0.872
	ARP/wARP	0.92	0.68	0.72	0.90	0.53	1.80	7.66	94.37	4.93	0.70	2.14	0.007	0.955
	Phenix	0.85	0.63	0.67	0.81	0.44	1.83	6.17	91.75	8.25	0	0	0.006	0.754
	Buccaneer	0.90	0.61	0.66	0.87	0.51	1.60	2.73	90.51	9.49	0	5.88	0.006	0.918
	Rosetta	0.79	0.51	0.54	0.77	---	1.47	1.32	87.32	11.27	1.41	7.35	0.007	1.007
Afp5	Foldit	0.86	0.72	0.75	0.83	0.54	1.13	1.25	95.92	4.08	0	0.69	0.007	0.738
	Microscopist	0.9	0.77	0.81	0.87	0.55	1.45	1.67	90.48	9.52	0	4.83	0.008	0.896
	ARP/wARP	0.88	0.75	0.79	0.85	0.55	2.06	8.38	87.91	10.23	1.86	8.53	0.08	1.493
	Phenix	0.83	0.69	0.73	0.78	0.42	1.95	4.14	78.45	21.55	0	6.73	0.008	1.225
	Buccaneer	0.84	0.70	0.74	0.80	0.50	1.72	4.82	92.41	7.59	0	3.05	0.009	1.167
	Rosetta	0.69	0.56	0.58	0.65	---	1.59	1.66	84.14	15.17	0.69	9.22	0.006	1.004
Afp7	Foldit	0.86	0.72	0.75	0.84	0.52	0.84	1.2	98.13	1.87	0	0.47	0.004	0.667
	Microscopist	0.87	0.75	0.79	0.85	0.50	1.83	4.81	88.79	11.21	0	8.02	0.006	1.082
	ARP/wARP	0.88	0.75	0.79	0.85	0.53	2.06	8.38	87.91	10.23	1.86	8.53	0.008	1.493
	Phenix	0.8	0.69	0.72	0.74	0.45	2.05	6.18	81.82	17.05	1.14	0	0.008	1.392
	Buccaneer	0.85	0.73	0.76	0.82	0.50	1.88	5.98	90.00	10.00	0	5.71	0.007	1.083
	Rosetta	0.66	0.44	0.47	0.61	---	1.6	2.1	87.02	12.98	0	6.5	0.005	0.863
Afp9	Foldit	0.85	0.75	0.78	0.83	0.47	1.06	2.75	98.21	1.79	0	1.82	0.009	0.829
	Microscopist	0.87	0.79	0.82	0.85	0.46	1.58	2.76	91.07	7.14	1.79	6.36	0.007	1.082
	ARP/wARP	0.86	0.78	0.81	0.84	0.47	2.19	10.27	86.11	13.89	0	11.32	0.007	0.952
	Phenix	0.83	0.73	0.76	0.8	0.41	1.68	2.78	87.18	12.82	0	5	0.006	1.042
	Buccaneer	0.81	0.69	0.72	0.78	0.41	2.00	5.21	80.85	17.02	2.13	6.67	0.009	1.251
	Rosetta	0.81	0.72	0.74	0.79	---	1.69	3.85	91.07	8.93	0	4.55	0.007	1.476

For each of the 4 different proteins, any method that outperformed the other 5 for a particular metric is shaded in green, with any method outperformed by the other 5 shaded red. CC_mask, CC_box, CC_peaks, and CC_volume are correlation coefficients calculated between the model and the map. The differences between these correlation coefficients arise from whether the entire map is used (CC_box), only the map around the atomic centers (CC_mask), the molecular envelope defined by the model (CC_volume), or the strongest peaks in the model and map (CC_peaks) [14]. CaBLAM uses the geometry of Cɑ atoms to evaluate low-resolution structures [35]. Clashscore reports on the number and severity of steric clashes in a model, and Molprobity score combines the Clashscore with other geometric factors to provide an overall evaluation of model quality [35].

AFP, antefeeding prophage; FSC, Fourier shell correlation; Rama., Ramachandran; RMSD, root mean square deviation

Fig 1. Comparison of model building for Afp7 in (A) an overall view and (B and C) views to compare side-chain fitting.

The Foldit structure is rendered in green, the microscopist structure in gray, the Phenix model in magenta, and Rosetta model in yellow. Because of the large deviations from the other structures, the Rosetta model is omitted in the zoomed-in views in parts B and C. The electron potential map is contoured at 2 σ. (D, E, and F) Comparison of key geometric and map fit parameters for each of the cases displayed here. (D) Comparison of Ramachandran outlier and allowed backbone conformations. (E) Comparison of Molprobity Clashscore—in both cases, lower is better. (F) Comparison of 3 different map-to-model correlation coefficients, in which higher values are better. More complete statistical analysis can be found in Table 1 and S8 Fig, with the underlying data provided in S1 Data. (G) Map-to-model FSC curves for Microscopist (gray), Foldit (green), Phenix (pink), ARP w/ARP (orange), and Buccaneer (blue) models. CC_mask, CC_box, CC_peaks, and CC_volume are correlation coefficients calculated between the model and the map. The differences between these correlation coefficients arise from whether the entire map is used (CC_box), only the map around the atomic centers (CC_mask), the molecular envelope defined by the model (CC_volume), or the strongest peaks in the model and map (CC_peaks) [14]. Afp7, antefeeding prophage 7; FSC, Fourier shell correlation; RMSD, root mean square deviation.

The Foldit score function appears to correctly reflect model quality. As expected, because of the absence of the phase problem, and unlike previous Foldit collaborations with crystallographic data [25,30], the structures from Foldit players that were the best in each puzzle as determined by Phenix validation [14] were also the best according to the Foldit score function, which is based on the Rosetta score function [31], with terms that model properties such as electrostatics, hydrogen bonds, solvation, and torsion angles, with an additional parameter that accounts for electron potential map fit. This observation suggests that by collaborating with Foldit, only minimal work will be required by microscopists to obtain an accurate, high-quality model.

Building models of large molecules into low-resolution data can be a time-consuming process for microscopists building structures by hand. However, in the 4 datasets presented here, Foldit players had arrived at finished structures in less than 48 hours (S16 Fig). Examining the workflow of Foldit players revealed that different players used distinct strategies in their model building. In the case of Afp9, the winning players chose to prioritize map fitting first and waited until the end to optimize the geometry of the structure (S1 Movie). Alternatively, in the case of Afp5, the winning players instead performed geometry optimization intermittently over the course of map fitting (S2 Movie). The general consensus—among the winning players who generated these 4 Foldit solutions—was to fold the protein “by hand” in the early stages of the puzzle and then run “recipes” (in-game algorithms written by the players) toward the end of the puzzle. Detailed accounts from all of the Foldit players who produced these 4 models are described in the “Foldit Player Testimonials” section in S2 Text.

These results indicate that there are multiple routes toward cryo-EM model building and that Foldit players could greatly speed the arduous model-building process for many cryo-EM projects. Although collaborating with Foldit players currently requires contacting the Foldit developers, future developments will include the ability for cryo-EM researchers the ability to communicate with Foldit players easily.

The strategy described here takes advantage of the collective ability of nonprofessional citizen scientists; however, the Foldit modeling tools are also available for individuals. Foldit Standalone runs offline on a single workstation and can be used by researchers to build and refine their structures with the Foldit scoring function [32]. Alternatively, Foldit Custom Contests can now be administered by researchers to allow online, collaborative model building and refinement among a research group or department or even a class of students [33]. Although we anticipate that for best results, researchers should draw on the collective expertise of the Foldit players, these other options may be attractive in the very competitive cryo-EM field.

To conclude, with the rapid improvement of cryo-EM map quality, it is now paramount for our building and refinement skills and tools to improve commensurably. Enlisting the help of citizen scientists, such as Foldit players, is one option to do so.

Materials and methods

To generate puzzles for Foldit players, the cryo-EM map (EMD-4782) sharpened with an overall b-factor of 105 Ų [34] was segmented around each fitted monomer of Afp1, Afp5, Afp7, and Afp9 (PDB 6rao, [34]), with a radius of 3 Šaround fitted atoms. For a detailed description of the Foldit puzzle setup and order, please see S1 Text. To calculate the FSC between models and map, a single version of an unfiltered, unsharpened segmented map was generated for each target by keeping a zone enclosing all fitted models (Microscopist, Rosetta, Phenix, Foldit) with a radius of 3 Šaround fitted atoms. The FSC was then calculated between the segmented map and a simulated map (up to Nyquist resolution with same pixel spacing) from each fitted model.

Ethics statement

Foldit has received IRB approval, and Foldit players provided informed consent to participate in research (University of Washington IRB STUDY00001238, titled: "Scientific Discovery Games").

Supporting information

S1 Data. Underlying key geometric and map fit parameters for data for Afp7.

(XLSX)

S2 Data. Underlying key geometric and map fit parameters for data for Afp1.

(XLSX)

S3 Data. Underlying key geometric and map fit parameters for data for Afp5.

(XLSX)

S4 Data. Underlying key geometric and map fit parameters for data for Afp9.

(XLSX)

S1 Table. Cα RMSDs between different models (in Å).

Rosetta and Buccaneer models not shown, as they were incomplete.

(DOCX)

S1 Fig

Comparison of model building for Afp1 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, the microscopist structure in gray, the Phenix model in magenta, and Rosetta model in yellow. Because of the large deviations from the other structures, the Rosetta model is omitted in the zoomed-in views in parts B and C. Electron potential map is contoured at 2 σ. Afp1, antefeeding prophage 1.

(PNG)

S2 Fig

Comparison of model building for Afp5 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, the microscopist structure in gray, the Phenix model in magenta, and Rosetta model in yellow. Because of the large deviations from the other structures, the Rosetta model is omitted in the zoomed-in views in parts B and C. Electron potential map is contoured at 2 σ. Afp5, antefeeding prophage 5.

(PNG)

S3 Fig

Comparison of model building for Afp9 in (A) an overall view, and (B and C) views to compare side- chain fitting. The Foldit structure is rendered in green, the microscopist structure in gray, the Phenix model in magenta, and Rosetta model in yellow. Because of the large deviations from the other structures, the Rosetta model is omitted in the zoomed-in views in parts B and C. Electron potential map is contoured at 2 σ. Afp9, antefeeding prophage 9.

(PNG)

S4 Fig

Comparison of model building for Afp1 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, ARP/wARP in orange, and Buccaneer in blue. Electron potential map is contoured at 2 σ. Afp1, antefeeding prophage 1.

(PNG)

S5 Fig

Comparison of model building for Afp5 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, ARP/wARP in orange, and Buccaneer in blue. Electron potential map is contoured at 2 σ. Afp5, antefeeding prophage 5.

(PNG)

S6 Fig

Comparison of model building for Afp7 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, ARP/wARP in orange, and Buccaneer in blue. Electron potential map is contoured at 2 σ. Afp7, antefeeding prophage 7.

(PNG)

S7 Fig

Comparison of model building for Afp9 in (A) an overall view, and (B and C) views to compare side-chain fitting. The Foldit structure is rendered in green, ARP/wARP in orange, and Buccaneer in blue. Electron potential map is contoured at 2 σ. Afp9, antefeeding prophage 9.

(PNG)

S8 Fig. Comparison of key geometric and map fit parameters for each of the tested cases for Afp7.

(A) Comparison of Ramachandran outlier and allowed backbone conformations. (B) Comparison of Molprobity Clashscore. (C) Comparison of 3 different map-to-model correlation coefficients. Underlying data for these graphs are provided in S1 Data. Afp7, antefeeding prophage 7.

(PNG)

S9 Fig. Comparison of key geometric and map fit parameters for each of the tested cases for Afp1.

(A) Comparison of Ramachandran outlier and allowed backbone conformations. (B) Comparison of Molprobity Clashscore. (C) Comparison of 3 different map-to-model correlation coefficients. Underlying data for these graphs are provided in S2 Data. Afp1, antefeeding prophage 1.

(PNG)

S10 Fig. Comparison of key geometric and map fit parameters for each of the tested cases for Afp5.

(A) Comparison of Ramachandran outlier and allowed backbone conformations. (B) Comparison of Molprobity Clashscore. (C) Comparison of 3 different map-to-model correlation coefficients. Underlying data for these graphs are provided in S3 Data. Afp5, antefeeding prophage 5.

(PNG)

S11 Fig. Comparison of key geometric and map fit parameters for each of the tested cases for Afp9.

(A) Comparison of Ramachandran outlier and allowed backbone conformations. (B) Comparison of Molprobity Clashscore. (C) Comparison of 3 different map-to-model correlation coefficients. Underlying data for these graphs are provided in S4 Data. Afp9, antefeeding prophage 9.

(PNG)

S12 Fig

Map versus model FSC curves for (A) Afp1, (B) Afp5, and (C) Afp9, comparing the Microscopist (gray), Foldit (green), and Phenix (purple) models. In each case, the hand-built models outperformed the Phenix and Buccaneer models, with the microscopist, ARP w/ARP, and Foldit models displaying similar fit. Afp, antefeeding prophage; FSC, Fourier shell correlation.

(PNG)

S13 Fig. Rosetta Energy versus GDT_TS plots for Foldit Puzzles 1554 and 1572: CASP13 target T1021s1 (the closer a model is to 1, on the right, the closer it matches the native fold).

(A) In Foldit puzzle 1554, players were unable to get close to the native state when only starting from server models without any experimental data. Each green point represents a Foldit player prediction. (B) In Foldit puzzle 1572, however, players were able to reach the native state when provided with a cryo-EM density map. cryo-EM, cryo-electron microscopy; GDT_TS, global distance test.

(PNG)

S14 Fig. Rosetta Energy versus GDT_TS plots for Foldit Puzzles 1579 and 1588: CASP13 target T1022s1 (the closer a model is to 1, on the right, the closer it matches the native fold).

(A) In Foldit puzzle 1579, players were unable to get close to the native state when only starting from server models without any experimental data. (B) In Foldit puzzle 1588, however, players were able to reach the native state when provided with a cryo-EM density map. cryo-EM, cryo-electron microscopy; GDT_TS, global distance test.

(PNG)

S15 Fig. Screenshot of starting state for Foldit Puzzle 1598.

Players were only given an extended chain along with the cryo-EM density map. cryo-EM, cryo-electron microscopy.

(PNG)

S16 Fig. Rosetta Energy versus GDT_TS plot of Foldit Puzzle 1598 (the closer a model is to 1, on the right, the closer it matches the native fold).

Starting from an extended chain, showing the progression of play over the first 2 days of the puzzle. Although no one was able to reach the native state in the first 24 hours (A), the native topology was found by the second day (B). GDT_TS, global distance test.

(PNG)

S17 Fig. Rosetta Energy versus GDT_TS plot of Foldit Puzzle 1598 after the puzzle ended (the closer a model is to 1, on the right, the closer it matches the native fold).

Final plot, after the puzzle closed, of the GDT_TS score versus the Rosetta Energy. GDT_TS, global distance test.

(PNG)

S18 Fig

Tracking Foldit player actions during Puzzle 1588: (A) Comments on shared player solutions. (B) Recipe additions to Notes for various segments.

(PNG)

S19 Fig. Poor player results from the first round (Puzzle 1579) without density as a guide.

Source: Foldit blog 10/16/18 https://fold.it/portal/node/2006086). A value of 1 represents a perfect match with the native.

(PNG)

S20 Fig. Starting by matching a tryptophan (“8” shape, top left) and related helix, and a phenylalanine (“9” shape, center) and related sheet.

The rest of the protein is cut out for visibility (bottom right).

(PNG)

S21 Fig. Hand-folding 1 hour and refining with recipes 24 hours almost every day.

(PNG)

S22 Fig. Two extra winning solutions shared to the group after the deadline by jeff101.

(A) The latest “B2p8” solution. (B) Latest “Batz” solution shared by player jeff101.

(PNG)

S1 Text. Supplemental Results.

(DOCX)

S2 Text. Foldit Player Testimonials from all 6 players who contributed to the 4 Foldit models.

(DOCX)

S1 Authors. Membership list of the Foldit Players consortium.

(DOCX)

S1 Movie. Winning players for Afp9 prioritized map fitting first over geometry optimization.

(MP4)

S2 Movie. Winning players for Afp5 performed geometry optimization intermittently during the puzzle.

(MOV)

Abbreviations

AFP

antefeeding prophage

cryo-EM

cryo-electron microscopy

FSC

Fourier shell correlation

RMSD

root mean square deviation

Rama

Ramachandran

Data Availability

All data and final models from this work can be found in Nat Microbiol. 2019 Aug 5. doi: 10.1038/s41564-019-0530-6 and related PDB entries. Intermediate structures are available by request. All underlying data for AFP7, presented in the bar graphs of Fig 1 and S8 Fig, can be found in the file S1 Data. All underlying data for AFP1, presented in the bar graphs of S9 Fig, can be found in the file S2 Data. All underlying data for AFP5, presented in the bar graphs of S10 Fig, can be found in the file S3 Data. All underlying data for AFP9, presented in the bar graphs of S11 Fig, can be found in the file S4 Data.

Funding Statement

This work was supported by the following 2 National Institutes of Health grants: R00 GM120388 (http://grantome.com/grant/NIH/R00-GM120388-03, SH) and 1UH2CA203780 (http://grantome.com/grant/NIH/UH2-CA203780-02, SC and FK). This material is based upon work supported by the National Science Foundation under grant no. 1629879 (https://www.nsf.gov/awardsearch/showAward?AWD_ID=1629879, SC). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.