Cryo-EM structure of SARS-CoV-2 ORF3a in lipid nanodiscs
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Abstract
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Jun Zhang, Bing Chen
Review 1: "Cryo-EM structure of the SARS-CoV-2 3a ion channel in lipid nanodiscs"
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Jun Zhang, Bing Chen
Review of "Cryo-EM structure of the SARS-CoV-2 3a ion channel in lipid nanodiscs"
Reviewer: Jun Zhang, Bing Chen (Boston Children's Hospital) | 📗📗📗📗◻️
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SciScore for 10.1101/2020.06.17.156554: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Experimental Models: Cell Lines Sentences Resources Cloning and protein expression: The coding sequence for the 3a protein from SARS-Cov-2 was codon optimized for Spodoptera frugiperda (Sf9 cells) and synthesized (IDT, Newark, NJ). Sf9suggested: CLS Cat# 604328/p700_Sf9, RRID:CVCL_0549)Constructs (2 μg) were transfected into HEK293 cells on glass coverslips using Fugene HD (Promega, Madison, WI) per manufacturer’s instructions. HEK293suggested: CLS Cat# 300192/p777_HEK293, RRID:CVCL_0045)Software and Algorithms Sentences Resources To calculate the total number of liposomes, we quantified the total number of liposomes using auto … SciScore for 10.1101/2020.06.17.156554: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Experimental Models: Cell Lines Sentences Resources Cloning and protein expression: The coding sequence for the 3a protein from SARS-Cov-2 was codon optimized for Spodoptera frugiperda (Sf9 cells) and synthesized (IDT, Newark, NJ). Sf9suggested: CLS Cat# 604328/p700_Sf9, RRID:CVCL_0549)Constructs (2 μg) were transfected into HEK293 cells on glass coverslips using Fugene HD (Promega, Madison, WI) per manufacturer’s instructions. HEK293suggested: CLS Cat# 300192/p777_HEK293, RRID:CVCL_0045)Software and Algorithms Sentences Resources To calculate the total number of liposomes, we quantified the total number of liposomes using auto segmentation on MetaXpress 6 from brightfield images. MetaXpresssuggested: (MetaXpress, RRID:SCR_016654)All statistical tests were performed using Prism (GraphPad). Prismsuggested: (PRISM, RRID:SCR_005375)GraphPadsuggested: (GraphPad Prism, RRID:SCR_002798)Cryo-EM data processing: For the apo 3a dimer, motion-correction and dose-weighting were performed on all 6,309 movies using RELION 3.1’s implementation of MotionCor2, and 2x “binned” to 1.137 Å per pixel49–51. RELIONsuggested: (RELION, RRID:SCR_016274)MotionCor2suggested: (MotionCor2, RRID:SCR_016499)A set of 86,479 particles were identified, polished in RELION3.1 and refined in cryoSPARC v2 with subsequent homogeneous and non-uniform refinement54 jobs (maps were low-pass filtered to an initial resolution where TM density was still visible (6-9 Å), and the dynamic mask was tightened with the near (2-5 Å) and far (3-9 Å) parameters), yielding a map with overall resolution of 3.6 Å. cryoSPARCsuggested: (cryoSPARC, RRID:SCR_016501)Molprobity61 was used to evaluate the stereochemistry and geometry of the structure for subsequent rounds of manual adjustment in Coot and refinement in Phenix. Phenixsuggested: (Phenix, RRID:SCR_014224)Cavity measurements were made with HOLE64 implemented in Coot. Cootsuggested: (Coot, RRID:SCR_014222)Figures were prepared using PyMOL, Chimera, ChimeraX66, Fiji, Prism, GNU Image Manipulation Program, and Adobe Photoshop and Illustrator software. PyMOLsuggested: (PyMOL, RRID:SCR_000305)Fijisuggested: (Fiji, RRID:SCR_002285)Image Manipulation Programsuggested: (GNU Image Manipulation Program, RRID:SCR_003182)Adobe Photoshopsuggested: (Adobe Photoshop, RRID:SCR_014199)Illustratorsuggested: (Adobe Illustrator, RRID:SCR_010279)The samples were excited with 488nm argon laser and image analysis was performed using ImageJ. ImageJsuggested: (ImageJ, RRID:SCR_003070)Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
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SciScore for 10.1101/2020.06.17.156554: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Experimental Models: Cell Lines Sentences Resources To test this , we generated an N-terminal deletion construct lacking the first 41 amino acids ( 3aΔN ) and compared its localization to wild-type 3a in HEK cells . HEKsuggested: CLS Cat# 300192/p777_HEK293, CVCL_0045Protein purification For preparation of the 3a dimer and mutant constructs , infected Sf9 cells from 1 L of culture ( 15-20 mL of cell pellet ) were thawed in 100 mL of Lysis Buffer containing 50 mM Tris , 150 mM KCl , 1mM EDTA pH 8 . Sf9suggested: NoneSciScore for 10.1101/2020.06.17.156554: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
NIH rigor criteria are not applicable to paper type.Table 2: Resources
Experimental Models: Cell Lines Sentences Resources To test this , we generated an N-terminal deletion construct lacking the first 41 amino acids ( 3aΔN ) and compared its localization to wild-type 3a in HEK cells . HEKsuggested: CLS Cat# 300192/p777_HEK293, CVCL_0045Protein purification For preparation of the 3a dimer and mutant constructs , infected Sf9 cells from 1 L of culture ( 15-20 mL of cell pellet ) were thawed in 100 mL of Lysis Buffer containing 50 mM Tris , 150 mM KCl , 1mM EDTA pH 8 . Sf9suggested: NoneConstructs (2 µg) were transfected into HEK293 cells on glass coverslips using Fugene HD (Promega, Madison, WI) per manufacturer’s instructions. HEK293suggested: CLS Cat# 300192/p777_HEK293, CVCL_0045Software and Algorithms Sentences Resources Cryo-EM data processing For the apo 3a dimer , motion-correction and dose-weighting were performed on all 6,309 movies using RELION 3.1’s implementation of MotionCor2 , and 2x “binned” to 1.137 Å per pixel30-32 . RELIONsuggested: (RELION, SCR_016274)<div style="margin-bottom:8px"> <div><b>MotionCor2</b></div> <div>suggested: (MotionCor2, <a href="https://scicrunch.org/resources/Any/search?q=SCR_016499">SCR_016499</a>)</div> </div> </td></tr><tr><td style="min-width:100px;vertical-align:top;border-bottom:1px solid lightgray">For the tetramer, the highest resolution reconstruction came from cryoSPARC v2 non-uniform refinement with a tightened mask, which was subsequently used for dimer-docking and figure preparation.</td><td style="min-width:100px;border-bottom:1px solid lightgray"> <div style="margin-bottom:8px"> <div><b>cryoSPARC</b></div> <div>suggested: (cryoSPARC, <a href="https://scicrunch.org/resources/Any/search?q=SCR_016501">SCR_016501</a>)</div> </div> </td></tr><tr><td style="min-width:100px;vertical-align:top;border-bottom:1px solid lightgray">Molprobity39 was used to evaluate the stereochemistry and geometry of the structure for subsequent rounds of manual adjustment in Coot and refinement in Phenix.</td><td style="min-width:100px;border-bottom:1px solid lightgray"> <div style="margin-bottom:8px"> <div><b>Phenix</b></div> <div>suggested: (Phenix, <a href="https://scicrunch.org/resources/Any/search?q=SCR_014224">SCR_014224</a>)</div> </div> </td></tr><tr><td style="min-width:100px;vertical-align:top;border-bottom:1px solid lightgray">Cavity measurements were made with HOLE41 implemented in Coot.</td><td style="min-width:100px;border-bottom:1px solid lightgray"> <div style="margin-bottom:8px"> <div><b>Coot</b></div> <div>suggested: (Coot, <a href="https://scicrunch.org/resources/Any/search?q=SCR_014222">SCR_014222</a>)</div> </div> </td></tr><tr><td style="min-width:100px;vertical-align:top;border-bottom:1px solid lightgray">Figures were prepared using PyMOL, Chimera, ChimeraX43 , Fiji, Prism, GNU Image Manipulation Program, and Adobe Photoshop and Illustrator software.</td><td style="min-width:100px;border-bottom:1px solid lightgray"> <div style="margin-bottom:8px"> <div><b>PyMOL</b></div> <div>suggested: (PyMOL, <a href="https://scicrunch.org/resources/Any/search?q=SCR_000305">SCR_000305</a>)</div> </div> <div style="margin-bottom:8px"> <div><b>Fiji</b></div> <div>suggested: (Fiji, <a href="https://scicrunch.org/resources/Any/search?q=SCR_002285">SCR_002285</a>)</div> </div> <div style="margin-bottom:8px"> <div><b>Image Manipulation Program</b></div> <div>suggested: (GNU Image Manipulation Program, <a href="https://scicrunch.org/resources/Any/search?q=SCR_003182">SCR_003182</a>)</div> </div> <div style="margin-bottom:8px"> <div><b>Adobe Photoshop</b></div> <div>suggested: (Adobe Photoshop, <a href="https://scicrunch.org/resources/Any/search?q=SCR_014199">SCR_014199</a>)</div> </div> <div style="margin-bottom:8px"> <div><b>Illustrator</b></div> <div>suggested: (Adobe Illustrator, <a href="https://scicrunch.org/resources/Any/search?q=SCR_010279">SCR_010279</a>)</div> </div> </td></tr><tr><td style="min-width:100px;vertical-align:top;border-bottom:1px solid lightgray">The samples were excited with 488nm argon laser and image analysis was performed using ImageJ.</td><td style="min-width:100px;border-bottom:1px solid lightgray"> <div style="margin-bottom:8px"> <div><b>ImageJ</b></div> <div>suggested: (ImageJ, <a href="https://scicrunch.org/resources/Any/search?q=SCR_003070">SCR_003070</a>)</div> </div> </td></tr></table>
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.
Results from OddPub: We did not find a statement about open data. We also did not find a statement about open code. Researchers are encouraged to share open data when possible (see Nature blog).
About SciScore
SciScore is an automated tool that is designed to assist expert reviewers by finding and presenting formulaic information scattered throughout a paper in a standard, easy to digest format. SciScore is not a substitute for expert review. SciScore checks for the presence and correctness of RRIDs (research resource identifiers) in the manuscript, and detects sentences that appear to be missing RRIDs. SciScore also checks to make sure that rigor criteria are addressed by authors. It does this by detecting sentences that discuss criteria such as blinding or power analysis. SciScore does not guarantee that the rigor criteria that it detects are appropriate for the particular study. Instead it assists authors, editors, and reviewers by drawing attention to sections of the manuscript that contain or should contain various rigor criteria and key resources. For details on the results shown here, including references cited, please follow this link.
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