Improving the DNA specificity and applicability of base editing through protein engineering and protein delivery

• Published in: Nature communications Vol. 8; no. 1; p. 15790
• Main Authors: Rees, Holly A., Komor, Alexis C., Yeh, Wei-Hsi, Caetano-Lopes, Joana, Warman, Matthew, Edge, Albert S. B., Liu, David R.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 06.06.2017; Nature Publishing Group; Nature Portfolio
• Subjects: 13; 42/41; 631/1647/1511; 631/337/4041/3196; 631/61/2297; 82; Animals; Cell Line; Chromatography; CRISPR-Cas Systems; DNA - genetics; DNA - metabolism; Editors; Gene Editing; Gene loci; Genomes; Humanities and Social Sciences; Laboratories; Mice; multidisciplinary; Mutation; Otology; Plasmids; Protein Engineering; Proteins; Ribonucleoproteins - genetics; Ribonucleoproteins - metabolism; Science; Science (multidisciplinary); Zebrafish; United States > US; Massachusetts
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms15790

We recently developed base editing, a genome-editing approach that enables the programmable conversion of one base pair into another without double-stranded DNA cleavage, excess stochastic insertions and deletions, or dependence on homology-directed repair. The application of base editing is limited by off-target activity and reliance on intracellular DNA delivery. Here we describe two advances that address these limitations. First, we greatly reduce off-target base editing by installing mutations into our third-generation base editor (BE3) to generate a high-fidelity base editor (HF-BE3). Next, we purify and deliver BE3 and HF-BE3 as ribonucleoprotein (RNP) complexes into mammalian cells, establishing DNA-free base editing. RNP delivery of BE3 confers higher specificity even than plasmid transfection of HF-BE3, while maintaining comparable on-target editing levels. Finally, we apply these advances to deliver BE3 RNPs into both zebrafish embryos and the inner ear of live mice to achieve specific, DNA-free base editing in vivo . Third-generation base editors consist of a catalytically disabled Cas9 fused to a cytidine deaminase and a base excision repair inhibitor, enabling efficient, precise editing of individual base pairs in DNA. Here the authors describe engineering and protein delivery of base editors to improve their DNA specificity and enable specific base editing in live animals.