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The ΦPA3 Phage Nucleus is Enclosed by a Self-Assembling, 2D Crystalline Lattice
Open accessPreprint — published as 10.1038/s41467-023-36526-9
Abstract
A growing number of jumbo bacteriophages, with genomes exceeding 200 kb, have been found to establish a Phage Nucleus—a micron-scale, proteinaceous structure encompassing the replicating phage DNA. Bacteriophage and host proteins associated with replication and transcription are concentrated inside the Phage Nucleus while nucleotide synthesis, translation, and numerous other host and exogenous proteins are effectively excluded, including CRISPR-Cas and restriction endonuclease host defense systems. Here, we show that fragments of the Phage Nucleus isolated from ΦPA3 infected Pseudomonas aeruginosa cells form a square lattice and demonstrate that the recombinantly purified primary Phage Nuclear Enclosure (PhuN) protein spontaneously assembles into sheets also constructed from a square lattice which we resolve to 3.8 Å by cryo-EM. Our structure reveals that the flexible termini and large loops mediate adaptable inter-tetramer contacts that drive shell assembly into a C2-symmetric lattice. While the interfaces between subunits are mostly well packed, two of the interfaces are open, forming clear channels that likely have important functional implications for the transport of proteins, mRNA and small molecules.
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
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Metadata
- Authors
- Nieweglowska, E., Brilot, A., Méndez-Moran, M., Baek, M., Li, J., Kokontis, C., Cheng, Y., Baker, D., Bondy-Denomy, J., & Agard, D.
- Affiliations
- University of California, San Francisco (US)
- University of California San Francisco
- University of Washington (US)
- Howard Hughes Medical Institute (US)
- University of California, San Francisco
- Corresponding author
- Agard, David
- ORCID
- Venue
- Nature Communications
- Published
- 2022-04-14
- Volume
- 14
- Issue
- 1
- Pages
- 927-927
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC9938867
- OpenAlex
- W4321328863
- Cited by
- 45
- References
- 1
- Citations by year
- 2026: 9 · 2025: 9 · 2024: 15 · 2023: 8 · 2022: 3
- FWCI
- 6.63
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- Research Square (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Howard Hughes Medical Institute (1S10OD021741, 1S10OD020054, 1S10OD026881)
- U.S. Department of Health and Human Services (R01AI171041, 1S10OD026881, R35GM140847, 1S10OD020054, R01GM127489, R35GM118099)
- W. M. Keck Foundation
- Washington Research Foundation
- Sandler Foundation
- Open Philanthropy Project
- National Institutes of Health (1s10od026881-01, 1s10od021741-01, NIH-R01, 1s10od020054-01)
- University of California, San Francisco (R35GM118099, 1S10OD021741, NIH P41-GM103311, P41-GM103311, 1S10OD026881, R35GM140847, 1S10OD020054, R01-GM129325)
- NIH Office of the Director (1S10OD026881, 1S10OD020054)
- National Institute of General Medical Sciences (R35GM118099, P41GM103311, R01GM127489, R35GM140847, T32GM139786, R01GM129325)
- National Institute of Allergy and Infectious Diseases (T32AI060537, R01AI171041)
- Topics
- Life Sciences › Immunology and Microbiology › Virology › Bacteriophages and microbial interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Keywords
- self-assembly, Pseudomonas aeruginosa, phage DNA replication, CRISPR-Cas, restriction enzymes
- MeSH terms
- Bacteriophages, Viral Proteins, CRISPR-Cas Systems
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