Streptococcus pyogenes (Spy) Cas9 has potential as a component of gene therapeutics for incurable diseases. One of its limitations is its large size, which impedes its formulation and delivery in therapeutic applications. Smaller Cas9s are an alternative, but lack robust activity or specificity and frequently recognize longer PAMs. Here, we investigated four uncharacterized, smaller Cas9s and found three employing a “GG” dinucleotide PAM similar to SpyCas9. Protein engineering generated synthetic RNA-guided nucleases (sRGNs) with editing efficiencies and specificities exceeding even SpyCas9 in vitro and in human cell lines on disease-relevant targets. sRGN mRNA lipid nanoparticles displayed manufacturing advantages and high in vivo editing efficiency in the mouse liver. Finally, sRGNs, but not SpyCas9, could be packaged into all-in-one AAV particles with a gRNA and effected robust in vivo editing of non-human primate (NHP) retina photoreceptors. Human gene therapy efforts are expected to benefit from these improved alternatives to existing CRISPR nucleases.
CRISPR systems evolved as a bacterial adaptive immune system in which resistance to phage infection is mediated by a nuclease (e.g., Cas9) that cleaves phage DNA. By exploiting the base-pairing potential of a guide RNA (gRNA), Cas9 targets a corresponding genomic locus for cleavage. A short motif on the targeted DNA, termed the protospacer adjacent motif (PAM), is necessary for Cas9 activity1,2,3,4. CRISPR-Cas9 has been harnessed as a versatile tool for directed genome editing5,6,7 and, with the above constraints, allows the targeting in principle of any given chromosomal region of interest.
Streptococcus pyogenes Cas9 (SpyCas9), the most common enzyme used in genome-editing applications, is a large nuclease of 1368 amino acid residues5. The advantages of SpyCas9 include its short, 5′-NGG-3′ PAM and very high average editing efficiency. Despite concerns about its specificity profile in some applications, the listed features have led SpyCas9 to be explored among the CRISPR nucleases of choice for clinical gene therapy applications8.
Effective delivery of CRISPR-Cas systems to targeted cells and tissues is crucial for successful in vivo genome editing. For this purpose, recombinant adeno-associated virus (rAAV) vectors and lipid-nanoparticles (LNPs) are among the most prevalent and promising technologies9. Because packaging into rAAV vectors is limited to ~5 kb, Cas9 proteins smaller than SpyCas9 are desirable to enable packaging of DNA encoding both Cas9 and sgRNA into one rAAV (“all-in-one-AAV”) particle. This limitation is exacerbated for the larger multidomain-Cas-nuclease-based systems for base editing, prime editing, or CRISPRi/a10,11,12,13,14. Beyond rAAVs, smaller nucleases can also facilitate formulation and mRNA manufacturing for LNPs15. Smaller Cas9 proteins are thus of keen interest in the field.
The best-characterized smaller Cas9 are from Staphylococcus aureus (SauCas9, 1053 amino acid residues)16 and Campylobacter jejuni (CjCas9, 984 amino residues)17. However, both recognize longer PAMs, 5′-NNGRRT-3′ for SauCas9 (R = A or G) and 5′-NNNNRYAC-3′ for CjCas9 (Y = C or T), which reduces the number of uniquely addressable target sites in the genome, in comparison to the NGG SpyCas9 PAM. First reports indicate that SauCas9 specificity is similar to SpyCas918,19.
Protein engineering and directed protein evolution have been successfully applied to improve a wide range of properties of many therapeutic and nontherapeutic proteins, including SpyCas920,21,22,23,24,25,26. Gene family DNA shuffling is a powerful protein optimization approach that leverages sequence diversity from homologous genes by randomly swapping gene fragments or polymorphisms to generate screenable gene-variant libraries20,22,23. This allows a myriad of perturbations of protein structure and function, while simultaneously maintaining a relatively high fraction of functional clones in the libraries20,21,22,23. The compounded effects of the perturbations in each clone can have minor to major effects on the encoded protein’s phenotype. Screening such a library can thus generate improvements involving combinations of a large number of simultaneous mutations, which are poorly accessible by other engineering approaches21,22.
Here, we apply gene family shuffling to four small Cas9 nucleases (~1050 amino acid residues). Our aim was to generate short, but highly active and specific, synthetic RNA-guided nucleases (sRGNs, pronounced “surgeons”) that recognize the favorable “GG” di-nucleotide PAM. Our resulting sRGNs displayed higher specificity and activity than SpyCas9 in human cell lines and robust in vivo editing in mice and nonhuman primates (NHP) when formulated as mRNA into LNPs, as well as when packaged as DNA into a single rAAV vector, thus making them well-suited candidates for gene therapy applications.
Characterization of four related small Cas9 nucleases
We examined four related, previously uncharacterized Cas9s from Staphylococcus hyicus (Shy), Staphylococcus lugdunensis (Slu), Staphylococcus microti (Smi), and Staphylococcus pasteuri (Spa), and found three recognized a favorable “NNGG” PAM (Supplementary Fig. 1). Among these, only SluCas9 displayed prominent genome-editing activity using ribonucleoprotein particles (RNP) directed to the HBB or the VEGFA locus in mammalian cell lines (Fig. 1a). The tracrRNA for all four parents were similar; however, upon assessing each of the four nucleases for activity with the SluCas9 tracrRNA, we observed increased genome editing only for ShyCas9 (Supplementary Fig. 2). The optimal guide length for SluCas9 was 21–23 nucleotides (Fig. 1b), similar to previous reports on SauCas916. Homology mapping to SpyCas9 and SauCas9 yielded predicted protein domains of the nucleases (Fig. 1c), facilitating the generation of nickases and inactive (“dead”) enzymes (Supplementary Fig. 1e).
Protein engineering and characterization of improved nucleases
To improve the editing efficiency and specificity of SluCas9, we applied DNA family shuffling. We fragmented and reassembled the above four “parental” genes at multiple areas of high sequence identity, resulting in two combinatorial sRGN DNA libraries with a diversity of 8 × 103 and 1.3 × 105, respectively (Fig. 2a). To retain favorable 5′-NNGG-3′ PAM recognition, the PAM-interacting domain (PID) in all library variants was initially held constant as the native SluCas9-PID. These libraries were prescreened using a “live/dead” bacterial survival assay, yielding an enriched library of 1824 active nucleases, which were further narrowed to 165 hits with superior cleavage kinetics using a cell-free cleavage assay (Fig. 2b, Supplementary Fig. 3a, b). These resulting 165 hits were subsequently assayed for activity in mammalian cells by BFP gene disruption (Fig. 2c). In line with previous observations25, we found generally weak correlation between the activities of a given engineered variant in the different screening assays (Fig. 2d). We thus selected the two top hits for each assay, respectively designated sRGN1-4, for further engineering (Supplementary Fig. 4a).
Further improvements in performance were explored by incorporating alternative PIDs. As stated above, we initially replaced PID domains of wild-type ShyCas9 with alternative Slu-PID fragments, resulting in chimeric nucleases that acquired the ability to cleave a 5′-NNGG-3′ PAM-containing target, in contrast to the Shy-native 5′-NNARMM-3′ PAM (Supplementary Fig. 4b). This motivated replacement of respective C-terminal fragments of the selected sRGNs with analogous fragments from either SpaCas9 or SmiCas9, since both also recognize a 5′-NNGG-3′ PAM. While tested SmiCas9 PID fusions were inactive, the SpaCas9 C-terminal fragments resulted in variable activity, depending on the recipient sRGN. All three SpaCas9-PID fragments resulted in active sRGN3 fusions, yielding sRGNs 3.1–3.3, and increased the median BFP-cleavage activity up to 2.8-fold (Fig. 2e). Substituting these PID fragments in the other three top variants yielded no similar benefit (Fig. 2e).
To assess the overall performance with a diverse set of sgRNAs, we then selected sRGN1, sRGN2, sRGN4, and sRGN3.3 for further testing on 11 targets distributed within the BFP locus. BFP protospacers were selected for either “NNGG” PAM for sRGNs and “NGG” PAM for SpyCas9, resulting in target sites shifted by one nucleotide. While plasmid transformation comparisons are suboptimal for detailed quantitative comparisons, sRGN1, 2, and 4 showed significant activity on most targets. Variant sRGN3.3 demonstrated higher cleavage activity in this assay, comparable to the highly active SpyCas9 (Fig. 2f).
SpyCas9 has been characterized to be, for practical purposes, a single-turnover enzyme, while the smaller SauCas9 exhibits multi-turnover activity26. In an in vitro assay with a twofold molar excess of substrate: RNP, sRGN3.1, and its parent, SluCas9, effected near-complete substrate-to-product conversion, indicating multi-turnover capability. For SpyCas9, in contrast, we confirmed single turnover activity (Supplementary Fig. 5a).
With few exceptions, insertion/deletion (indel) pattern analysis of SluCas9, sRGN3.3, and SpyCas9 revealed similarities among these nucleases on the same targets (Supplementary Fig. 5b), supporting previous observations that indel formation pattern is more dependent on target locus than employed nuclease24.
Synthetic RNA-guided nuclease (sRGN) activity and specificity in cell-free and mammalian cell line assays
RNPs are attractive, therapeutically relevant entities for ex vivo cellular genome editing, especially due to their limited duration of activity resulting from the faster cellular turnover of Cas9 proteins vs. rAAV genomic DNA or plasmids. Using RNPs, we determined 22 nt as the optimal guide length for sRGN3.1 (Fig. 3a) and detected approximately two-fold higher potency for sRGN3.1 over SluCas9 at the HBB_R01 target in mammalian cells in gRNA titration experiments (Fig. 3b). Additionally, higher cleavage activity of sRGN3.1 and sRGN3.3 compared to SpyCas9 was observed on the albumin locus in a murine hepatoma cell line (Supplementary Fig. 6). We next assessed editing on a panel of endogenous, superimposed SpyCas9 and sRGN targets (adjacent to 5′-NNGGG-3′ PAMs) on 24 diverse targets in HEK293T cells (Fig. 3c). The average editing efficiency across these targets was 2.3-fold (SluCas9) and 3.1-fold (sRGN3.1) higher than for SpyCas9 (Fig. 3c, right panel). Additionally, we performed a cell-free FP assessment on 48 synthetic target sequences engineered to have between 20 and 80% GC content, and on 48 additional therapeutically relevant human genomic targets. Overall, we found the protein-engineered sRGN3.1 outperformed SpyCas9 on 76 of these 96 targets and outperformed its most active parental nuclease, SluCas9, on 62 of 96 targets (Supplementary Fig. 7a).
Off-target (OT) cleavage is an important parameter in clinical applications. To initially characterize our sRGNs’ propensities for OT cleavage, we analyzed their cleavage behavior in vitro using each possible single-nucleotide gRNA mismatch along the entire HBB_R01 target sequence (Supplementary Fig. 7b). Confirming previous reports27, we observed that SpyCas9 showed low mismatch discrimination (low specificity) outside of its PAM-proximal “seed” region. SluCas9 showed overall specificity similar to SpyCas9 but with a less pronounced seed region and higher specificity in the PAM distal region. sRGN3.1 also lacked a prominent seed region, but instead showed an improved average level of mismatch discrimination across the entire protospacer region in comparison to SpyCas9.
To probe the specificity of sRGN3.1, SluCas9, and SpyCas9 in a human cell line, GUIDE-Seq28 was employed. We selected well-characterized guides targeting the VEGFA_T229 or HBB_R01_T230 locus and dosed RNP activity to achieve similar on-target editing for each nuclease (Supplementary Fig. 7d). As expected, the on-target in each case yielded the highest number of reads. For SpyCas9, we recovered 66 unique off-targets using the VEGFA_T2 guide (of which 50 had been previously reported31) and 82 OTs using the HBB_R01 guide. Consistent with our described cell-free observations, we found greatly reduced OT editing for SluCas9 (30 using VEGFA_T2, 2 for HBB_-R01) and an even greater specificity increase for sRGN3.1 (2 and 1 OTs, respectively). This was even the case in samples for which the extent of on-target editing was greater for sRGN3.1 and SluCas9 than for Spy. Extending the guide length from 20 to 22 nt further reduced the number of OTs from 30 to 15 for SluCas9 on VEGFA_T2, and from 1 to 0 for sRGN3.1 on HBB_R01_T2 (Supplementary Fig. 7d and Fig. 3d). sRGN3.1 thus displayed significantly higher specificity than SpyCas9 in this context.
In vivo genome editing by sRGNs using LNP and AAV
Lipid nanoparticles are a current modality of choice to transiently deliver nucleases for genome editing applications in vivo. We thus evaluated the performance of sRGNs when delivered as mRNA in LNPs. Analyses using UPLC (Supplementary Fig. 8a) and cryoTEM (Supplementary Fig. 8b) showed differences in final lipid composition and improved LNP morphology, which appeared to be payload-dependent and which we hypothesize were due to the smaller sRGN mRNA. Interestingly, the sRGN-LNPs also displayed enhanced functional stability, retaining potency significantly longer than SpyCas9-LNPs. Over 9 days of storage at 2–8 °C, a 3.6-fold drop in editing efficiency was observed with SpyCas9-LNPs, whereas a potency drop of only 1.3-fold was observed with sRGN-LNPs, resulting in an over 3.6-fold superiority in in vivo editing efficiency for the sRGN over SpyCas9 after 9 days of storage (Supplementary Fig. 8c).
We next compared LNP-mediated editing of the albumin locus by sRGNs and SpyCas9 in cells, as well as in the liver of C57BL/6 mice (Fig. 4a). Similar to the performance in cells (Supplementary Fig. 6), LNPs harboring sRGN3.1 mRNA displayed editing comparable to SpyCas9 in vivo, while sRGN3.3 was less efficient in this experiment. In addition, we tested the in vivo effects of mRNA sequence and chemistry modifications, including uridine depletion32 and base substitution of uridine. Modification with (N1)-methylpseudouridine (m1Ψ) or with pseudouridine (Ψ) had only modest influence on in vivo editing outcome (Supplementary Fig. 8d). Alternative modifications of the sgRNAs enhanced in vivo performance, with the utilization of a 23-mer protospacer showing the largest effect on gene editing efficiency (Supplementary Fig. 8e).
In addition to LNP delivery, we evaluated AAV-based delivery, since the smaller size of sRGNs provides a packaging advantage over the larger SpyCas9. Usher syndrome type II (USH2) is an autosomal recessive disorder leading to hearing loss and retinitis pigmentosa33. This is caused by mutations in the USH2A gene, which is expressed in cochlear hair and retinal photoreceptor cells. One commonly found mutation in USH2 patients (termed IVS40) results in the insertion of an additional exon in USH2A mRNA, leading to premature truncation of the gene product33. We used sRGN3.1 and SpyCas9 to address the IVS40-specific mutation in an IVS40 homozygous cell line (referred to as 293FT-IVS40, also see Methods section). On-target editing in the 293FT-IVS40 line was higher for sRGN3.1 than for SpyCas9 (Supplementary Fig. 9b). Upon examining specificity by GUIDE-Seq and targeted amplicon sequencing of OT sites with up to seven nucleotide substitutions from the on-target site, we identified no OT editing above background for either SpyCas9 or sRGN3.1 (see amplicon sequencing data in the source data file, tab Supplementary Fig. 9a).
Toward clinical applications in humans, we tested the editing efficiency of rAAV-delivered sRGN3.1 in nonhuman primate (NHP) photoreceptors (PR) in vivo. As our NHP model possessed only the WT-USH2A allele, we pursued a surrogate strategy, assessing sRGN3.1 activity using a WT-specific USH2A guide (Supplementary Fig. 9b).
Of note, the larger size of SpyCas9 precludes an all-in-one approach. Comparison with SpyCas9 would require generation and co-injection of two rAAV5-genomes, one encoding the SpyCas9 nuclease and the second encoding the guide RNA expression components. Ethical considerations of a poorly comparable control in the NHP model thus led us to exclude SpyCas9 from this experiment.
The smaller size of sRGN3.1 allowed its packaging together with sgRNA into single AAV5 particles. We injected these particles into the NHP subretinal space and quantified indels in PRs. Six and twelve weeks after injection, we counted robust sRGN3.1-mediated in vivo editing in NHP-PRs (Fig. 4b). In summary, this result establishes successful AAV delivery of the compact sRGN3.1 gene, which was co-packaged with its sgRNA in single AAV vector particles, and allows for substantial genome editing in NHP photoreceptor cells.
Here we report the generation and characterization of programmable small RNA-guided nucleases, which are smaller than SpyCas9, but with hgiher activity and specificity. Mouse studies with LNPs and AAV-mediated gene therapy in NHP show the potential of these additions to the CRISPR toolbox.
The packaging size limitation of AAV vectors and potential benefits from formulating smaller mRNA payloads into LNPs has generated considerable interest in genome-editing nucleases smaller than the widely used SpyCas934,35. However, these smaller alternatives to SpyCas9 typically show lower editing efficiencies on average across diverse targets in human cells and/or possess more complex PAM sequences, which further limit their utility18,36,37. SauCas9 is similar in size to the presently described sRGNs, but has a less advantageous PAM, and engineered forms of SauCas9 struggle with lower activity on certain targets38. Of note, Kleinstiver et al. observed an average editing of 24.7% across 55 targets sites, while sRGN3.1 presented here shows an average editing of 41% across the 24 tested target sites. CjeCas9, although 74 amino acids smaller17, has not reached widespread use, potentially due to its long and degenerate PAM, which reduces the number of genomic sites targetable. Additionally, a recent paper in Science Advances39 raised important concerns about the enzyme, as it was shown to exhibit guide-independent, nonspecific host-cell DNA damage. In contrast, Nme2Cas9 is a small “CC” PAM nuclease. Importantly, unlike the sRGNs described in this work, the authors of the Nme2 paper find Nme2 inferior to SpyCas9 on 24 out of 28 sites tested40. Other recently published hypercompact enzymes such as Cas14 and CasPhi41,42 are of interest in the field, even if no genome-editing activity on native (i.e., endogenous) genes in mammalian cells has yet been reported and no head-to-head comparison with SpyCas9 has been conducted. In addition, time fluorescence disruption activity assays like the ones reported here suggest they may be inferior to SpyCas9. Furthermore, we are not aware of reports outlining the specificity of CasPhi in a mammalian setting. Finally, the presence of a single nuclease domain in this protein makes it unlikely that it can be modified for the strand-specific nickase activity required for base editing or prime editing applications. By contrast, sRGN3.1, the product of this work, constitutes a chimeric dual-nuclease domain enzyme that recognizes a short 5′-NNGG-3′ PAM, and which outperformed SpyCas9 regarding activity and specificity on the majority of tested targets.
We are aware of no reports to date of an alternative Cas9 nuclease with on-target editing efficiency comparable to SpyCas9 across a range of genomic targets. sRGN3.1 was determined to have a median activity 17% higher than SpyCas9 on 24 targets selected for analysis only by virtue of an associated NGGG motif. Using LNPs delivered i.v. to the mouse liver, we demonstrated that the in vivo albumin-locus target activity of sRGNs was comparable to SpyCas9. However, this comparison employed a 20 nt guide for both nucleases, rather than the optimal guide length for sRGN3.1. In separate experiments (Fig. 1b and Supplementary Fig. 8e) median sRGN activity in vivo was boosted significantly with 23 nt guides. In addition, RNA base modifications were also shown to boost sRGN activity in vivo. Together, these results indicate sRGNs are an attractive payload that can be effectively delivered by LNPs for robust in vivo gene editing.
High specificity is of critical importance in gene therapy applications. The undesirable properties of off-target (OT) activity43,44 and the resulting undesired mutations and/or chromosome rearrangements45 have been attributed to the high activity of SpyCas9. Nevertheless, data on the small SauCas9 are suggestive that this lower-activity nuclease has similar specificity to SpyCas916. Our GUIDE-Seq experiments revealed specificity for sRGN3.1 that was markedly higher than for SpyCas9, despite both being titrated to similar on-target editing efficiency. Indeed, these observations were made in immortalized cell line backgrounds that have been shown to more sensitively reveal genomic OT propensities of editing nucleases than primary human cells46,47,48. Interestingly, it appears that in engineering higher activity into sRGN3.1, we relaxed stringency at certain PAM-proximal positions in comparison to SluCas9, the highest activity WT nuclease in our parental set, while simultaneously increasing PAM-distal specificity, at least for the target investigated in depth (Supplementary Fig. 7b). While sRGNs and SpyCas9 both performed well in discriminating the few genomic off-targets possessing one or two mismatches to the on-target gRNA (Supplementary Fig. 7b), there will typically be exponentially more genomic off-targets with three or four mismatches than with one or two. Despite the very high-specificity seed region of SpyCas9, the dispersed base-pairing requirement across the sRGN3.1 gRNA appeared to better serve it in discriminating off-targets with multiple mismatches (Fig. 7b, d). Although higher overall specificity was observed for sRGN3.1 in vitro, an additional hypothesis for its much higher specificity in mammalian cells may paradoxically include the engineered sRGN’s higher activity: the requirement for fewer nuclease molecules per cell may contribute to the more rapid elimination of the nuclease and thus less opportunity for off-target effects.
Effective in vivo delivery of genome editing agents remains challenging for some applications, despite recent commercial successes34,49,50. We thus investigated LNP and rAAV in vivo delivery approaches for sRGN3.1. sRGN LNPs had comparable or improved analytical and stability profiles to SpyCas9-LNPs. Further investigation is required to understand if the improved properties observed can be attributed solely to the packaging advantages of smaller RNA payloads. The toxicity of LNP formulations has been shown highly dependent on administered lipid quantities51, which also may be improved with equal editing activity in smaller RNA payloads (higher RNA stoichiometry per unit LNP mass). In addition, RNA quality in such formulations is also key and mRNA cost and product quality are typically improved with shorter constructs52. The smaller sRGNs are thus also more attractive than SpyCas9 from a biopharmaceutical manufacturing and quality perspective.
AAVs present another clear case for the size-based advantages of sRGN payloads. The large size of SpyCas9 requires the packaging of Cas9 and its sgRNA into two separate AAV vectors, increasing manufacturing complexity and potentially decreasing therapeutic efficacy in some use cases53. We demonstrated that subretinal injection of sRGN3.1 as an all-in-one rAAV5 affected robust editing in NHP photoreceptors in vivo.
In summary, we engineered potent, small, genome-editing nucleases that recognize a favorable PAM. We demonstrated targeted genome cleavage efficiency equal or superior to the “activity gold-standard” SpyCas9, across a broad selection of targets in human cell lines. In addition, sRGNs showed markedly higher specificity in GUIDE-Seq experiments in human cell lines. Robust in vivo editing efficiency was observed for LNP delivery in mice and AAV5 delivery in NHP. For a given therapeutically relevant genomic locus, our data indicate that sRGN3.1 has a higher probability of being more active and more specific, while offering the delivery advantages of a smaller nuclease. We thus expect that these synthetic RNA-guided nucleases will be valuable additions to the current repertoire of CRISPR gene therapy nucleases, and look forward to the implementation of these enzymes in a range of applications.
Identification of Cas9 sequences
Four uncharacterized, putative Cas9 nucleases with ~80% amino acid similarity and ~65% amino acid identity from shotgun sequencing data in Uniprot for four Staphylococcus species were identified: S. hyicus (Shy) GB: CP008747.1, Uniprot: A0A418JLD8, S. lugdunensis (Slu) NCBI reference sequence: NZ_GL622352.1, Uniprot: A0A133QCR3, S. microti (Smi) GB: JXWY01000132.1, Uniprot: A0A0D6XNZ8, and S. pasteuri (Spa) GB: CP004014.1 (see also Supplementary Table 2). Direct repeat and tracr sequences were identified by inspection. We exploited GAAA tetraloop fusion of crRNA and tracrRNA, as previously reported5,16, to form single-guide RNAs (sgRNAs). DNA sequences for sgRNAs and nucleases were codon optimized and ordered at GeneArt and Twist Biosciences.
Screening of libraries
In an initial “live/dead” (L/D) cell survival selection in E. coli54, we depleted nonfunctional or low-activity variants (Supplementary Fig. 3b and 3c). E.coli BW25141(λDE3) cells harboring a plasmid-based arabinose-inducible ccdB reporter gene were co-transformed with an expression plasmid for sgRNA (targeting VEGFA-T2 within the ccdB reporter) and an IPTG-inducible nuclease expression plasmid. Cells were recovered for 60 min in SOB media and subsequently plated on LB selection plates (chloramphenicol and 10 mM arabinose). Functional Cas9 variants cleaved the toxic ccdB reporter gene and led to cell survival under selection conditions. In all, 1824 functional clones from the L/D selection were expressed in E. coli and lysates were individually tested for activity in a biochemical oligodeoxynucleotide (ODN) cleavage assay (Supplementary Fig. 3d).
E. coli-based negative selection assay for identification of Cas9 PAM specificities
The negative selection for identification of PAM specificities of generated Cas9s was done as previously described54. Briefly, competent E. coli BL21Star(λDE3) containing an IPTG inducible Cas9 (AmpR) and a sgRNA (KanR) expression plasmid were electroporated with a library of plasmids (CmR) harboring a VEGFA_T2 target sequence with 3′ adjacent N7 PAM sequences. Plasmids containing functional PAMs are depleted when Cas9 is induced, whereas plasmids harboring nonfunctional PAMs remain uncleaved. Following a 60 min recovery in SOB media, transformations were plated on LB plates in two sets: one induced (ampicillin, kanamycin, chloramphenicol, and 0.2 mM IPTG) and one not induced (ampicillin, kanamycin, chloramphenicol) set. In order to exceed the complexity (16,384) of the N7 library, approximately 100,000 CFUs were plated, and plasmids were isolated using Plasmid DNA Midiprep Kit (Qiagen). From the resulting plasmid libraries, a 271 bp fragment covering the VEGFA_T2 target and N7 PAM was amplified by PCR using KOD Hot Start DNA Polymerase (Merck Millipore) with primers fw: 5′-CTCAGAAGTGAAACGCCGTAGCG-3′ and rev: 5′-CTTTTGAGTGAGCTGACACCGCTC-3′ followed by a PCR-product purification step with QIAquick PCR Purification Kit (Qiagen). Single-indexed libraries were prepared using the TruSeq DNA PCR-Free High Throughput Library Prep Kit (Illumina). Next-generation sequencing (NGS) was performed using a MiSeq reagent kit v3 with 600 bp paired-end sequencing on an Illumina MiSeq Sequencer. The resulting raw FASTQ files from the MiSeq runs were analyzed with a python script to determine relative PAM depletion. Shortly, this involves scripts to (1) process crude NGS Data for VEGFA_T2 target sequence [Each FASTQ entry is scanned for 12 constant nucleotides on the library amplicon on both strands. If the constant region is found, then the seven variable nucleotides flanking the protospacer region are captured and multiples are counted.]; (2) calculate depletion values by comparing PAM sequence motifs of depleted samples to undepleted controls and; (3) rank sequences according to frequency.
Fluorescence polarization assay
Oligonucleotide duplexes (oligo sequences are listed in Supplementary Table 3) were prepared in 1× PBS + 5 mM MgCl2 as 10 µM solutions (from 100 µM stocks) by melting at 95 °C for 5 min and then slowlycooling to room temperature (RT). The stocks were subsequently diluted in 1× PBS + 5 mM MgCl2 + 0.05% pluronic F68 (Sigma Aldrich) to 20 nM working solutions. Twenty microlitres (20 nM) of dsDNA was immobilized on a streptavidin-coated plate (Greiner, 384-well) and incubated for 10 min at RT. The plate was washed twice with 1X PBS and was subsequently incubated with 20 µL of a diluted lysate supplemented with 60 nM sgRNA targeting the VEGFA_T2 target sequence. Cas9 variants were expressed in 800 µL TB (Terrific Broth)-medium, as described in the protein expression and purification section, at the 96-well expression scale. Cells were harvested and lysed in 120 µL lysis buffer (1× PBS + 0.5 × BugBuster® + 5 mM MgCl2) and incubated for 10 min at RT under shaking conditions. The lysate was cleared by centrifugation: 3166 × g, 10 min at 4 °C. Cleared lysate was diluted 1:3.5 (v/v) in 1× PBS + 5 mM MgCl2 and mixed with 60 nM sgRNA, prior to a 5 min incubation at 37 °C. Cleavage was monitored by following both decreasing anisotropy and increasing fluorescence intensity for 60 min (excitation wavelength: 635 nm; emission wavelength: 670 nm) at 37 °C in a plate reader (Tecan Infinite M1000 pro). For activity specificity assessment of purified protein, prior to the kinetic measurement, RNPs were formed in 1× PBS + 5 mM MgCl2, with a two-fold excess of sgRNA at 37 °C for 5 min with adjusted protein levels for the same activity. To obtain an overall specificity value, the cleavage kinetics were analyzed by calculating the initial slope of the reaction. The slopes were calculated for each of the 61 substrates (including the un-modified sequence and all single-nucleotide exchanges along the VEGFA_T2 target sequence) and normalized to the value of the on-target substrate. For position-specific nucleotide tolerance profiles, the cleavage kinetics were analyzed by calculating the initial slope of the oligonucleotide cleavage reaction. The slopes were calculated for each of the 61 substrates and normalized to the value of the on-target substrate (defined as 1). The normalized cleavage values for all 60 off-target substrates were grouped according to their position. For each of the 20 nucleotide positions in the target sequence, the normalized cleavage value of the three single nucleotide mismatches was plotted to illustrate the position-specific nucleotide tolerance of the Cas9 protein.
Expression and purification of Cas9 proteins
Cas9 proteins were expressed from a plasmid harboring a TRC-promoter expression cassette, encoding an N-terminal 6xHis-MBP-TEV fusion followed by a nucleoplasmin NLS and a C-terminal SV40 NLS. E. coli BL21 (DE2) star was transformed with the expression construct and a single colony was grown overnight at 37 °C in ZY-medium (including 21.5 ml of 52 × 5052 solution (0.5% glycerol, 0.05% glucose, and 0.2% α-lactose), 52.5 ml of 20xNPS, and 2 mM MgSO4) supplemented with 100 µg/mL ampicillin. One liter of supplemented ZY-medium was inoculated 1:100 (v/v) with the overnight culture and shaken at 37 °C for 3 h. After 3 h, the culture was cooled to 18 °C and incubated overnight. IPTG in a final concentration of 1 mM was added, and the culture was incubated for two additional days. The cells were harvested by centrifugation (4376 × g, 20 min, 4 °C), the cell pellet was resuspended in 22 mL wash buffer (50 mM Na2HPO4 300 mM NaCl, 10 mM imidazole, pH 8.0) and lysed under sonification 10 min on ice (amplitude 30). The lysate was cleared by centrifugation (194300 × g, 30 min, 4 °C) and applied to His-Trap HP columns (GE healthcare) using the ÄKTA pure system (GE healthcare) to perform an immobilized metal affinity chromatography (IMAC) step. After two washing steps, first with wash buffer including 0.1% triton, then with wash buffer only, the protein was eluted with a linear gradient of 10–500 mM imidazole. Pooled protein fractions were subsequently treated with TEV at 4 °C for 2 days to cleave off the His-MBP tag. After 48 h, the protein solution was buffer exchanged into equilibration buffer (20 mM HEPES, 100 mM KCl, pH 7.0) using PD-10 columns (GE healthcare) and a cation exchange chromatography was performed by using HiTrap SP HP columns (GE healthcare) with a linear gradient of 100–1000 mM KCl (20 mM HEPES, 1000 mM KCl, pH 7.0). Before protein fractions were pooled, quality and purity were checked via SDS-PAGE, and a biochemical cleavage assay was conducted to exclude fractions with inactive nuclease contaminations. Nuclease activity used in downstream assays was standardized by sgRNA titrations. Briefly, starting from an excess of sgRNA, the amount of sgRNA was reduced, until a decrease in activity was observed. Fractions were pooled, concentrated, and stored in storage buffer (20 mM HEPES, 200 mM KCl, 1 mM DTT, 40% glycerol pH 7.0) at –20 °C.
RNP formation was performed with 20 µL of gRNA (800 nM stock) in 20 µL of 1x NEB buffer and heated to 90 °C for 3 min and cooled to 25 °C at 1 C/s. RNP was formed by combining 20 µL of this gRNA with 20 µL of Cas9 in 1x NEB buffer at a stock concentration of 200 nM the final concentration was 100 nM Cas and 200 nM gRNA. The concentration of active Cas9 was determined55 before kinetic analysis for enzymes that were obtained commercially or synthesized in house. This solution was incubated at 25 °C in a thermal cycler for 30 min prior to use. On-target reactions: 8 µL of off-target plasmid (250 nM stock) was combined with 10 µL of 10x NEB buffer and 72 µL of RNase-free water. This solution was placed on a heat block at 37 °C and the reaction was initiated by adding 10 µL of the RNP stock. Quenching and analysis: At various time points, 5 µL of the reaction was removed and quenched with 2 µL of a 500 mM EDTA solution. Once all samples were collected, RNP was removed by adding 1 µL of proteinase K to each reaction. Samples were analyzed on an Agilent 2100 Bioanalyzer using a DNA 7500 kit.
HEK293T cells (ref. CRL-3216) and murine Hepa 1–6 cells (ref. CRL-1830) were purchased from ATCC and 293FT cells were purchased from Thermo Fisher Scientific (ref. R70007).
HEK293T, 293FT, and homozygous 293FT-IVS40 cell lines were cultured in DMEM-GlutaMAX (Gibco) supplemented with 10% FBS (Gibco), and 1% sodium pyruvate (Gibco) and were cultured at 37 °C in 5% CO2. Hepa 1–6 cells were cultured in DMEM (Gibco) supplemented with 10% FBS (Gibco) and 1% penicillin-streptomycin (Gibco) at 37 °C with 5% CO2.
293FT-IVS40 cell lines were constructed as follows: to introduce the single nucleotide substitution corresponding to IVS40, TrueCut Cas9 Protein v2 complexed with TrueGuide synthetic sgRNA (Thermo Fisher Scientific) and 200-nucleotide ssODN (5′-TCAGCCAGAGCAGGAAGCTAATAAAATGTATGCTGGCTTTTAAGGGGGAAACAAATCATGAAATTGAAATTGAACACCTCTCCTTTCCCAAGGTAAGAGATCATCTTTAAGAAAAGGCTGTGTATTGTGGGGGTTTGAAGTGCAAGTTCATCTCATTATCATGGATGTTTCACCCATAATACTATCATCATATGCAGGAG -3′) were used for stable transfections. Transfected cells were cultured as serial dilutions and screened by Sanger sequencing to isolate homozygous clones.
Plasmid, mRNA, and RNP transfection, harvesting, and lysis
For BFP disruption assay and indel pattern analysis, 15,000 HEK 293T cells/well were seeded the day before transfection in poly-d-lysine-coated 96-well plates (Biocoat Poly-d-Lysine, Fisher Scientific). On the next day, a medium change was performed, which was followed by the transfection of 140 ng Cas9- or sRGN-expression plasmid plus 60 ng gRNA-expression plasmid using LipoD293 (SignaGen) as a transfection reagent according to the manufacturer’s instructions. The medium was changed 24 h later. Seventy-two hours post transfection medium was removed, and cells were trypsinized in 25 µL TrypLE (Gibco) for 15 min at 37 °C and diluted with 100 µL PBS. Ten microliters of the sample was lysed by adding 0.5 µl DNA Release additive (B93, Thermo Fisher Scientific) and 20 µL Dilution buffer (F1325ML, Thermo Fisher Scientific) and incubated for 5 min at room temperature followed by 98 °C for 2 min. For mRNA transfection, murine Hepa 1–6 cells were plated in 24-well plates at a density of 50,000 cells per well. After incubation for 2 hr, cells were transfected with 0.25 µg of nuclease mRNA and 0.25 µg of sgRNA per well using Lipofectamine MessengerMAX (Thermo Fisher Scientific) by following the manufacture′r’s instructions. Cells were collected 3 days after transfection and genomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen) following the manufacturer’s instructions. Parental 293FT and the homozygous IVS40 293FT cell line (2 × 105 cells) were transfected with 2 µg of a sRGN3.1 expression plasmid and with either T428 sgRNA or T428 surrogate sgRNA by using Lipofectamine 3000 (Thermo Fisher Scientific Scientific). Genomic DNA was extracted 7 days after transfection with DNeasy Blood & Tissue Kit (Qiagen). A fragment containing the editing region was amplified using PCR with the appropriate primers (Supplementary Table 3) and used for TIDE analysis.
For Ribonucleoprotein (RNP) complex formation, crRNA and tracrRNA (IDT, phosphorothioate bonds, and 2'-O-methyl groups at the last two nucleotides, see Supplementary Table 1 for sequences) were dissolved in IDTE buffer at 200 µM and mixed at equimolar ratios to obtain 100 µM working solution. The crRNA:tracrRNA duplex was incubated at 95 °C for 5 min and gradually cooled to 4 °C. To prepare Cas9/sRGN-RNP complexes, Cas9/sRGN protein was incubated with crRNA:tracrRNA duplex at a 1:2 molar ratio. Cas9/sRGN and RNA complex was incubated in 10 mM TRIS at RT for 15 min to form RNP complexes. 2 × 105 cells were washed with 1X PBS (Gibco), detached with Accutase (Sigma), spun down by centrifugation at 300xg for 5 min, washed again with 1X PBS and nucleofected with precomplexed RNPs using the 4D nucleofector with the SF cell line kit and program CA-137 (Lonza), according to the manufacturer’s protocol. Cells were seeded on poly-d-lysine-coated 24-well plates (Biocoat Poly-d-Lysine, Corning) and harvested 2–3 days after nucleofection by 15 min TrypLE (Gibco) incubation at 37 °C. Genomic DNA from RNP-treated cells was extracted with QIAamp DNeasy Blood & Tissue Kit (Qiagen) according to the manufacturer’s instructions.
BFP disruption assay
This assay was adapted based on the previously described traffic light assay56. Briefly, HEK293T cells harboring a gene encoding BFP in the AAVS1 locus were transfected with plasmid expressing Cas9 and a sgRNA targeting the reverse strand of BFP genomic sequence (guide_5 for initial screens). Transfection of plasmids was performed using Lipofectamine 3000 (Thermo Fisher Scientific, Cat no. L3000015) as described by the supplier. Flow cytometric analyzes of BFP signal disruption was carried out 7 days posttransfection as follows. Cells were prepared by washing with 1X PBS, trypsinization, and resuspension in 200 µL FACS buffer (1X PBS supplemented with 2% FCS). BFP signal from minimum of 10,000 cells was assayed using the V450 filter set in the BD FACS Canto II (see Supplementary Fig. 1 for gating strategy). For BFP landscaping analysis sRGNs guide_5-17 and Spy guide_19-31 were used. We switched from the initial T7 promoter spacer (5′-TATA-3′) to the more canonical U6 spacer (5′-AAACACC-3′) for these experiments. Gating strategy is presented in Supplementary Fig. 10.
Amplicon sequencing (AmpSeq) for on- and off-target analysis and NGS analysis
To assess the editing efficiency or to evaluate predicted off-targets, a ~200–240 bp fragment flanking the genomic target site was amplified by PCR using Q5 High-Fidelity polymerase (2XMM Master Mix (NEB), 1 µL crude cell lysate or 50 ng purified genomic DNA, and barcoded primers (see Supplementary Table 3 for locus-specific primers). The cycling program was performed according to the manufacturer’s instructions with an annealing temperature of 66 °C and an extension time of 15 s. All PCR reactions were pooled into a library and purified with magnetic beads (AMPure XP beads, Beckman Coulter). Bead purification was performed by applying the following reaction steps. Two micrograms of the pooled amplicons were end-repaired and dA-tailed (NEBNext Ultra II End Repair/dA-tailing Module, NEB) and used for ligation of Illumina indices (Blunt/TA Ligase master Mix, NEB). The concentration was measured using the dsDNA HS Kit (Thermo Fisher Scientific) on a Qubit spectrophotometer and diluted to 4 nM. The library was denatured with 0.2 M NaOH for 5 min at RT and diluted to 10 pM using the buffer provided in the MiSeq 300PE v2 Kit. The sample was sequenced with 12.5 pmol PhiX on a MiSeq Instrument (Illumina). For de-multiplexing an in-house python script was used and individual samples were analyzed using CRISPResso V1.0.1357 to extract % NHEJ. A threshold of >20,000 reads was chosen.
Evaluation of off-target sites at the USH2A locus
Forty-nine sites containing up to five nucleotide substitutions from the T428 target sites were selected for analysis. The homozygous IVS40 293FT cell line (2 × 105 cells) was transfected with 2 µg of a plasmid carrying sRGN3.1 and T428 sgRNA in Lonza SF buffer by nucleofection under Program CM-130, and genomic DNA was extracted 7 days after nucleofection. All the selected sites except one on-target site were successfully PCR-amplified, and indels were analyzed by NGS as described in the section Amplicon sequencing (AmpSeq) and NGS analysis.
Digital droplet PCR
In order to determine editing rates, ddPCR (Bio-Rad) was performed with 50 ng genomic DNA by using ddPCR supermix for probes (no dUTP, Biorad). Droplet formation was accomplished by (Biorad) QX200 Droplet Generator Amplification was done by using the following primers, probes, and annealing temperatures in a 40 cycle program with an additional extension step of 72 °C (HBB_R01: amplification primer fw 5′-catggtgcatctgactcctg-3′, rev 5′-ggtagaccaccagcagccta-3′, NHEJ-sensitive-probe 5′-TGAAGTTGGTGGTGAGGCCCT-3′, reference probe 5′-AGGAGAAGTCTGCCGTTACTGCCCT-3′, annealing temperature 58.5 °C). Analysis was performed on the QX200 ddPCR Reader (Biorad).
GUIDE-seq experiments were performed as previously described28. For off-target analyses on the USH2A (IVS40) locus, the homozygous IVS40 293FT cell line (2 × 105 cells) was nucleofected with 5 pmol of dsODN and 2 µg of a plasmid carrying sRGN3.1 and T428 sgRNA in Lonza SF buffer by nucleofection under Program CM-130. Genomic DNA was extracted 3 days after nucleofection using the PureLink Genomic DNA Mini Kit (Thermo Fisher Scientific Scientific), and processed for sequencing as previously described28.
Briefly, HEK293T cells were transfected with nuclease and sgRNA as RNPs as described above with addition of 5 pmol phosphorothioate (PS) end-protected double-stranded oligonucleotide (dsODN). For VEGFA_T2 and HBB_R01 off-target analysis we observed higher activities of SluCas9 and sRGN3.1 compared to SpyCas9 on these targets. Therefore, we used 60 pmol SpyCas9 and 30 pmol each of SluCas9 and sRGN3.1 for targeting HBB_R01, except for sRGN3.1 with 22 nt guide, 8 pmol were used. For targeting VEGFA_T2, 60 pmol SpyCas9, 8, and 18 pmol sRGN3.1 (for 20 nt and 22 nt guide, respectively) and 6 and 10 pmol SluCas9 (for 20 nt and 22 nt guide, respectively) were used to obtain a similar extent of on-target editing for each nuclease (Supplementary Fig. 7c). Genomic DNA was extracted 48 h upon nucleofection with DNeasy Blood & Tissue Kit (Qiagen) and on-target activity of nucleases was evaluated via amplicon sequencing as described above. Genomic DNA was quantified by Qubit dsDNA BR assay (Invitrogen) and 400 ng sample was sheared with NEBNext UltraII FS enzyme mix (NEBNext UltraII FS DNA Library Prep Kit, NEB) for 10 min at 37 °C, followed by 30 min inactivation at 65 °C. Sample libraries were constructed with NEBNext Ultra II DNA Library Prep Kit (NEB) with adapters and primers previously described28. Sample libraries were sequenced with Illumina MiSeq. Similar read-depth samples were analyzed with the open-source software package guideseq28 (https://github.com/aryeelab/guideseq commit version c608522), using human genome assembly GRC37/hg19 as reference.
Evaluation of editing efficiencies on the USH2A and Alb locus was done via TIDE (Tracking of indels by decomposition)58 analysis. Targeted-specific amplicon products were generated with 50–100 ng template DNA and primers spanning the target site (listed in Supplementary Table 3). Indels were identified via decomposition of quantitative trace data with the TIDE software (https://tide.nki.nl), using default parameters.
LNP formulation and characterization
The LNPs used in this study comprised a lipid mixture consisting of C12-200 (amino lipid, Axolabs), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), DMPE-mPEG2000 (PEG-lipid), and cholesterol at a 52.2:15.6:8.7:23.6 mass ratio, respectively (DOPE, PEG-lipid, and cholesterol from Avanti Polar Lipids). LNPs were prepared by rapid microfluidic mixing (Precision NanoSystems) of mRNA and sgRNA in acetate buffer at pH 4.0 with the lipid mixture suspended in ethanol (3:1 aqueous to organic volume ratio). After mixing, LNPs were diluted and dialyzed into PBS, concentrated as needed using 100k MWCO spin cartridges (Amicon), and 0.2 µm sterile filtered. mRNA production and sequence optimization was performed as previously described32,59. gRNA was procured from Synthego (sRGN Alb-T1), Avecia (SpyCas9 Alb-T1), and Agilent (modified sRGN Alb-T1 constructs). LNPs were characterized by dynamic light scattering (DLS) using a Wyatt Nanostar, Ribogreen (Thermo Fisher Scientific), for endotoxin (Endosafe, Charles River), by UPLC (Thermo Fisher Scientific), and cryoTEM (MIT) assays.
This study complied with all applicable sections of the Final Rules of the Animal Welfare Act regulations (Code of Federal Regulations, Title 9), the Public Health Service Policy on Humane Care and Use of Laboratory Animals from the Office of Laboratory Animal Welfare, and the Guide for the Care and Use of Laboratory Animals from the National Research Council. The protocol and any amendments or procedures involving the care or use of animals in this study was reviewed and approved by the Testing Facility Institutional Animal Care and Use Committee before the initiation of such procedures. Testing Facility Institutional Animal Care and Use Committee: Charles River Laboratories, Mattawan, Michigan 49071 (Macaca fascicularis) and Mispro Biotech Services, Inc. (C57BL/6j). C57BL/6j mice, age: 6 to 8 weeks old, sex: male, source: bred in captivity at Jackson Laboratories, Bar Harbor, Maine, Origin: Jackson Laboratories, Bar Harbor, Maine. Macaca fascicularis, age: 2–4 years old, weight: 2.5–5.0 kg, sex: male, source: bred in captivity at World Wide Primates, Inc., Origin: Mainland Asia.
Mouse studies to assess liver editing by LNPs
Animals were housed on a 12:12 h light/dark cycle at an ambient mean temperature of 23 °C and humidity at 50%. Experimental procedures were approved by the Institutional Animal Care and Use Committee (IACUC) review board. C57BL/6 animals (6–8 week-old male mice) were obtained from Jackson Laboratories (Bar Harbor, ME). For all mouse studies, animals were injected with a single intravenous dose of LNP-formulated mRNA and sgRNA through the tail vein, and after 96 h ± 5% mice were euthanized for genome-editing analysis. Whole liver was flash-frozen in liquid nitrogen, homogenized and genomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen) according to the manufacturer’s instructions. A fragment containing the editing region was amplified using PCR and used for TIDE analysis.
Subretinal injection of AAV5 vectors and analysis of genome editing in photoreceptors of nonhuman primates
The Photoreceptor-specific GRK1 promoter was chosen to limit Cas9 expression to photoreceptors60,61. A U6 promoter-driven T428 surrogate sgRNA, and the sRGN3.1 gene under GRK1 promoter were inserted between AAV2 ITRs and packaged in AAV5 capsids. The AAV5 vector was diluted to 1 × 1012 or 2 × 1012 vg/mL with phosphate-buffered saline containing 0.001% F68. The animals were anesthetized, and the eyes prepared for insertion of two 25-gauge scleral ports 3 mm posterior to the limbus. An endoilluminator probe was inserted in one port and a subretinal injection cannula was inserted through the second port. The subretinal injection cannula was advanced to mid-vitreous and the small diameter injection cannula was advanced until it contacted the retinal surface. AAV5 vector solution of volume 0.1 mL was slowly delivered to induce a subretinal bleb. Once the dose was delivered, the injection cannula and endoilluminator were removed, the scleral ports were removed, and the sclerotomies were sealed using electrocautery.
Retinal punch biopsy
Following enucleation, the anterior chamber, lens, and vitreous humor from each eye were removed. Four radial cuts were made in the eyecup to flatten the globe. The subretinal bleb and a portion of the neurosensory retina distal to the bleb were collected with a 6–8 mm biopsy punch. The samples were snap-frozen on dry ice. Frozen retinal samples were pulverized using a Geno/Grinder 2010 (SPEX SamplePrep, LLC) at 1500 revolutions per minute for 2 min. The homogenized tissue was suspended in phosphate-buffered saline (PBS) and split into three tubes. Genomic DNA was extracted from approximately one-third of the retinal samples using QIAamp DNA Mini Kit (Qiagen), and indels were quantified by NGS as described above.
Statistical analysis and curve-plotting were conducted using GraphPad Prism 8. Where applicable, normal distribution was determined before suitable downstream statistical analysis using D’Agostino & Pearson test. Unless stated otherwise, *p < 0.05, **p < 0.01, ***p < 0.001.
WO2019183150 covers sRGN3.1, SpaCas9, ShyCas9, and SmiCas9 sequences. Status: pending. Applicant: CRISPR Therapeutics AG, Bayer Healthcare LLC. Inventors: COHNEN, André, SCHMIDT, Moritz J., COCO, Wayne M., GAMALINDA, Michael B., GUPTA, Ashish, PITZLER, Christian, RICHTER, Florian, TEBBE, Jan, CHENG, Christopher J., TAKEUCHI, Ryo, REISS, Caroline W.
WO2019118935 covers SluCas9. Status: pending. Applicant: CRISPR Therapeutics AG, Bayer Healthcare LLC. Inventors: COHNEN, André, SCHMIDT, Moritz J., COCO, Wayne M., GUPTA, Ashish, TEBBE, Jan, SCHULENBURG, Cindy, PITZLER, Christian, GAMALINDA, Michael B. JACH, Sabine, RICHTER, Florian, ARUMUGHAN, Anup, SAALWÄCHTER, Corinna.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
All data generated or analyzed during this study are included in this published article and its supplementary information files and are available from the corresponding author upon reasonable request. Parental Staphylococcus can be accessed on Uniprot. S. hyicus (Shy) GB: CP008747.1, Uniprot: A0A418JLD8, S. lugdunensis (Slu) NCBI reference sequence: NZ_GL622352.1, Uniprot: A0A133QCR3, S. microti (Smi) GB: JXWY01000132.1, Uniprot: A0A0D6XNZ8 and S. pasteuri (Spa) GB: CP004014.1. Sequences of engineered proteins used herein are available in Supplementary Table 2. NGS data of this study have been deposited in the Sequence Read Archive (SRA) at NCBI with the project number PRJNA731307. Source data are provided with this paper.
All published algorithms used in this study are referenced in the Methods section. Custom-made algorithms are available from the corresponding author upon request. Supplementary Software is available with this manuscript.
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The authors thank the following: Sabine Jach, Astrid Meyer, Helen Dietmar, Corinna Saalwächter, Katharina Schäfer, Viktoria Bazilyanska, Danuta Cichon and Anjanette Pickbrenner for molecular biology and assay support. Rike Wallbrecher for support with BFP disruption assays. Randi Mackler and Dominik Ziehe for protein purification and the execution and implementation of cell free assays. Keith Abe, Valerie Guerrero, Cornell Mallari, Luis Gamboa, and TeQuana Bayless for support with mouse experiments. Philipp Knyphausen, Andreas Neerincx, Gregory J. Cost, Alan Brooks, Karen Vo, Chad Cowan, Thomas J. Cradick, Tony Ho, John Kulman for thoughtful scientific discussions and suggestions. Hemangi Chaudhari, Soeren Turan, Eric G. Anderson and Brian Fochtman for critically reading the manuscript. Barbara Wan and Lisa Geller for alliance management and project support.
A.C., M.J.S., W.M.C., M.G., A.G., C.P., F.R., J.T., C.J.C., R.T., C.W.R., K.W., K.K., A.K., A.S., A.N., S.S. have filed patent applications through Bayer AG, Casebia LLC, and CRISPR Therapeutics on the results described herein. A.C., W.M.C., M.G., K.K., A.G., M.L., S.J.S., C.P., M.S., J.T. hold stock or shares in the affiliated companies.
Peer review information Nature Communications thanks the anonymous reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Schmidt, M.J., Gupta, A., Bednarski, C. et al. Improved CRISPR genome editing using small highly active and specific engineered RNA-guided nucleases. Nat Commun 12, 4219 (2021). https://doi.org/10.1038/s41467-021-24454-5
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