8QWD
Apo ReChb
Summary for 8QWD
| Entry DOI | 10.2210/pdb8qwd/pdb |
| EMDB information | 18691 18692 18693 18694 |
| Descriptor | ReChb, MAGNESIUM ION (3 entities in total) |
| Functional Keywords | cas, biosynthetic protein, cryo-em, ancestral sequence reconstruction, biotechnology |
| Biological source | synthetic construct |
| Total number of polymer chains | 1 |
| Total formula weight | 149002.72 |
| Authors | Lopez-Alonso, J.P.,Ubarretxena-Belandia, I.,Tascon, I. (deposition date: 2023-10-19, release date: 2024-10-02, Last modification date: 2024-11-13) |
| Primary citation | Jabalera, Y.,Tascon, I.,Samperio, S.,Lopez-Alonso, J.P.,Gonzalez-Lopez, M.,Aransay, A.M.,Abascal-Palacios, G.,Beisel, C.L.,Ubarretxena-Belandia, I.,Perez-Jimenez, R. A resurrected ancestor of Cas12a expands target access and substrate recognition for nucleic acid editing and detection. Nat.Biotechnol., 2024 Cited by PubMed Abstract: The properties of Cas12a nucleases constrict the range of accessible targets and their applications. In this study, we applied ancestral sequence reconstruction (ASR) to a set of Cas12a orthologs from hydrobacteria to reconstruct a common ancestor, ReChb, characterized by near-PAMless targeting and the recognition of diverse nucleic acid activators and collateral substrates. ReChb shares 53% sequence identity with the closest Cas12a ortholog but no longer requires a T-rich PAM and can achieve genome editing in human cells at sites inaccessible to the natural FnCas12a or the engineered and PAM-flexible enAsCas12a. Furthermore, ReChb can be triggered not only by double-stranded DNA but also by single-stranded RNA and DNA targets, leading to non-specific collateral cleavage of all three nucleic acid substrates with similar efficiencies. Finally, tertiary and quaternary structures of ReChb obtained by cryogenic electron microscopy reveal the molecular details underlying its expanded biophysical activities. Overall, ReChb expands the application space of Cas12a nucleases and underscores the potential of ASR for enhancing CRISPR technologies. PubMed: 39482449DOI: 10.1038/s41587-024-02461-3 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.33 Å) |
Structure validation
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