Abstract
Protein-primed DNA replication is a unique mechanism, bioorthogonal to other known DNA replication modes. It relies on specialised single-stranded DNA (ssDNA)-binding proteins (SSBs) to stabilise ssDNA intermediates by unknown mechanisms. Here, we present the structural and biochemical characterisation of P12, an SSB from bacteriophage PRD1. High-resolution cryo-electron microscopy reveals that P12 forms a unique, cooperative filament along ssDNA. Each protomer binds the phosphate backbone of 6 nucleotides in a sequence-independent manner, protecting ssDNA from nuclease degradation. Filament formation is driven by an intrinsically disordered C-terminal tail, facilitating cooperative binding. We identify residues essential for ssDNA interaction and link the ssDNA-binding ability of P12 to toxicity in host cells. Bioinformatic analyses place the P12 fold as a distinct branch within the OB-like fold family. This work offers new insights into protein-primed DNA replication and lays a foundation for biotechnological applications.
| Original language | English |
|---|---|
| Article number | gkaf132 |
| Number of pages | 15 |
| Journal | Nucleic Acids Research |
| Volume | 53 |
| Issue number | 5 |
| Early online date | 7 Mar 2025 |
| DOIs | |
| Publication status | Published - 24 Mar 2025 |
Bibliographical note
© The Author(s) 2025. Published by Oxford University Press on behalf of Nucleic Acids Research.Keywords
- DNA, Single-Stranded/metabolism
- Cryoelectron Microscopy
- Viral Proteins/chemistry
- Protein Binding
- DNA-Binding Proteins/chemistry
- Bacteriophages/genetics
- Models, Molecular
- DNA Replication
- Binding Sites
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