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dc.contributor.authorGoulet, Adeline
dc.contributor.authorCAMBILLAU, Christian
dc.date.accessioned2024-02-22T16:44:48Z
dc.date.available2024-02-22T16:44:48Z
dc.date.issued2022-05-09
dc.identifier.issn2296-889X
dc.identifier.pmid35615740
dc.identifier.doi10.3389/fmolb.2022.907452
dc.identifier.urihttp://hdl.handle.net/10147/640897
dc.descriptionIn 2021, the release of AlphaFold2 - the DeepMind's machine-learning protein structure prediction program - revolutionized structural biology. Results of the CASP14 contest were an immense surprise as AlphaFold2 successfully predicted 3D structures of nearly all submitted protein sequences. The AlphaFold2 craze has rapidly spread the life science community since structural biologists as well as untrained biologists have now the possibility to obtain high-confidence protein structures. This revolution is opening new avenues to address challenging biological questions. Moreover, AlphaFold2 is imposing itself as an essential step of any structural biology project, and requires us to revisit our structural biology workflows. On one hand, AlphaFold2 synergizes with experimental methods including X-ray crystallography and cryo-electron microscopy. On the other hand, it is, to date, the only method enabling structural analyses of large and flexible assemblies resistant to experimental approaches. We illustrate this valuable application of AlphaFold2 with the structure prediction of the whole host adhesion device from the Lactobacillus casei bacteriophage J-1. With the ongoing improvement of AlphaFold2 algorithms and notebooks, there is no doubt that AlphaFold2-driven biological stories will increasingly be reported, which questions the future directions of experimental structural biology.en_US
dc.description.abstractIn 2021, the release of AlphaFold2 - the DeepMind's machine-learning protein structure prediction program - revolutionized structural biology. Results of the CASP14 contest were an immense surprise as AlphaFold2 successfully predicted 3D structures of nearly all submitted protein sequences. The AlphaFold2 craze has rapidly spread the life science community since structural biologists as well as untrained biologists have now the possibility to obtain high-confidence protein structures. This revolution is opening new avenues to address challenging biological questions. Moreover, AlphaFold2 is imposing itself as an essential step of any structural biology project, and requires us to revisit our structural biology workflows. On one hand, AlphaFold2 synergizes with experimental methods including X-ray crystallography and cryo-electron microscopy. On the other hand, it is, to date, the only method enabling structural analyses of large and flexible assemblies resistant to experimental approaches. We illustrate this valuable application of AlphaFold2 with the structure prediction of the whole host adhesion device from the Lactobacillus casei bacteriophage J-1. With the ongoing improvement of AlphaFold2 algorithms and notebooks, there is no doubt that AlphaFold2-driven biological stories will increasingly be reported, which questions the future directions of experimental structural biology.
dc.language.isoenen_US
dc.rightsCopyright © 2022 Goulet and Cambillau.
dc.subjectAlphaFold2en_US
dc.subjectLactobacillus casei bacteriophage J-1en_US
dc.subjectbacteriophageen_US
dc.subjectbacteriophage-host interactionsen_US
dc.subjecthost adhesion deviceen_US
dc.subjectstructural biologyen_US
dc.titlePresent Impact of AlphaFold2 Revolution on Structural Biology, and an Illustration With the Structure Prediction of the Bacteriophage J-1 Host Adhesion Device.en_US
dc.typeArticleen_US
dc.identifier.journalFrontiers in molecular biosciencesen_US
dc.identifier.pmcidPMC9124777
dc.source.journaltitleFrontiers in molecular biosciences
dc.source.volume9
dc.source.beginpage907452
dc.source.endpage
refterms.dateFOA2024-02-22T16:44:49Z
dc.source.countrySwitzerland


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