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Improving SARS-CoV-2 structures: Peer review by early coordinate release.
Croll, Tristan I; Williams, Christopher J; Chen, Vincent B; Richardson, David C; Richardson, Jane S.
  • Croll TI; CIMR, University of Cambridge, Cambridge, United Kingdom.
  • Williams CJ; Department of Biochemistry, Duke University, Durham, North Carolina.
  • Chen VB; Department of Biochemistry, Duke University, Durham, North Carolina.
  • Richardson DC; Department of Biochemistry, Duke University, Durham, North Carolina.
  • Richardson JS; Department of Biochemistry, Duke University, Durham, North Carolina. Electronic address: jane.richardson@duke.edu.
Biophys J ; 120(6): 1085-1096, 2021 03 16.
Article in English | MEDLINE | ID: covidwho-1033766
ABSTRACT
This work builds upon the record-breaking speed and generous immediate release of new experimental three-dimensional structures of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) proteins and complexes, which are crucial to downstream vaccine and drug development. We have surveyed those structures to catch the occasional errors that could be significant for those important uses and for which we were able to provide demonstrably higher-accuracy corrections. This process relied on new validation and correction methods such as CaBLAM and ISOLDE, which are not yet in routine use. We found such important and correctable problems in seven early SARS-CoV-2 structures. Two of the structures were soon superseded by new higher-resolution data, confirming our proposed changes. For the other five, we emailed the depositors a documented and illustrated report and encouraged them to make the model corrections themselves and use the new option at the worldwide Protein Data Bank for depositors to re-version their coordinates without changing the Protein Data Bank code. This quickly and easily makes the better-accuracy coordinates available to anyone who examines or downloads their structure, even before formal publication. The changes have involved sequence misalignments, incorrect RNA conformations near a bound inhibitor, incorrect metal ligands, and cis-trans or peptide flips that prevent good contact at interaction sites. These improvements have propagated into nearly all related structures done afterward. This process constitutes a new form of highly rigorous peer review, which is actually faster and more strict than standard publication review because it has access to coordinates and maps; journal peer review would also be strengthened by such access.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peer Review / SARS-CoV-2 Type of study: Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biophys J Year: 2021 Document Type: Article Affiliation country: J.bpj.2020.12.029

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peer Review / SARS-CoV-2 Type of study: Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Biophys J Year: 2021 Document Type: Article Affiliation country: J.bpj.2020.12.029