Patent Application
20210363518
This disclosure relates to compositions and methods of modified guide RNAs for CRISPR genome editing.
CRISPR RNA-guided genome engineering has revolutionized research into human genetic disease and many other aspects of biology. Numerous CRISPR-based in vivo or ex vivo genome editing therapies are nearing clinical trials. At the heart of this revolution are the microbial effector proteins found in class II CRISPR-Cas systems such as Cas9 (type II) and Cas12a/Cpf1 (type V) (Jinek et al. Science 337, 816-821 (2012); Gasiunas et al. PNAS 109, E2579-E2586 (2012); Zetsche et al. Cell 163, 759-771 (2015)).
The most widely used genome editing tool is the type II-A Cas9 from Streptococcus pyogenes strain SF370 (SpCas9) (Jinek et al, supra). Cas9 forms a ribonucleoprotein (RNP) complex with a CRISPR RNA (crRNA) and a trans-activating crRNA (tracrRNA) for efficient DNA cleavage both in bacteria and eukaryotes (
For mammalian applications, Cas9 and its guide RNAs can be expressed from DNA (e.g. a viral vector), RNA (e.g. Cas9 mRNA plus guide RNAs in a lipid nanoparticle), or introduced as a ribonucleoprotein (RNP). Viral delivery of Cas9 results in efficient editing, but can be problematic because long-term expression of Cas9 and its guides can result in off-target editing, and viral vectors can elicit strong host immune responses (Mingozzi et al. Blood 122, 23-36 (2013)). RNA and RNP delivery platforms of Cas9 are suitable alternatives to viral vectors for many applications and have recently been shown to be effective genome editing tools in vivo (Yin et al. Nature Biotechnology 35, 1179 (2017); Lee et al. eLife 6, e25312 (2017)). RNP delivery of Cas9 also bypasses the requirement for Cas9 expression, leading to faster editing. Furthermore, Cas9 delivered as mRNA or RNP exists only transiently in cells and therefore exhibits reduced off-target editing. For instance, Cas9 RNPs were successfully used to correct hypertrophic cardiomyopathy (HCM) in human embryos without measurable off-target effects (Ma et al. Nature 548, 413 (2017).
The versatility of Cas9 for genome editing derives from its RNA-guided nature. The crRNA of SpCas9 usually includes a 20 nucleotide guide region followed by a 16 nucleotide repeat region (
The present disclosure provides chemically modified guide RNAs for CRISPR genome editing. In certain embodiments, the guide RNAs of the disclosure are heavily or fully chemically modified. The guide RNA of the disclosure may confer several advantages in vivo or ex vivo, including stability, improved potency, and/or reduced off-target effects. Furthermore, in certain embodiments, the modified RNAs of the disclosure have reduced immunogenicity, e.g., a reduced ability to induce innate immune responses.
In certain aspects, the disclosure provides a chemically modified guide RNA comprising: (a) a crRNA portion comprising (i) a guide sequence capable of hybridizing to a target polynucleotide sequence, and (ii) a repeat sequence; and (b) a tracrRNA portion comprising an anti-repeat nucleotide sequence that is complementary to the repeat sequence, wherein the chemically modified guide RNA comprises at least 80% modified nucleotides.
In an embodiment, the one or more modified nucleotides each independently comprise a modification of a ribose group, a phosphate group, a nucleobase, or a combination thereof.
In an embodiment, each modification of the ribose group is independently selected from the group consisting of 2′-O-methyl, 2′-fluoro, 2′-deoxy, 2′-O-(2-methoxyethyl) (MOE), 2′-NH2, a bicyclic nucleotide, a locked nucleic acid (LNA), a 2′-(S)-constrained ethyl (S-cEt), a constrained MOE, or a 2′-0,4′-C-aminomethylene bridged nucleic acid (2′,4′-BNANN).
In an embodiment, at least 80% of the ribose groups are chemically modified.
In an embodiment, each modification of the phosphate group is independently selected from the group consisting of a phosphorothioate, phosphonoacetate (PACE), thiophosphonoacetate (thioPACE), amide, triazole, phosphonate, or phosphotriester modification.
In an embodiment, each modification of the nucleobase group is independently selected from the group consisting of 2-thiouridine, 4-thiouridine, N6-methyladenosine, pseudouridine, 2,6-diaminopurine, inosine, thymidine, 5-methylcytosine, 5-substituted pyrimidine, isoguanine, isocytosine, or halogenated aromatic groups.
In an embodiment, the guide RNA comprises at least 90% modified nucleotides.
In an embodiment, the guide RNA comprises 100% modified nucleotides.
In an embodiment, a plurality of the nucleotides at positions 1-10, 20-21, and 27-36 from the 5′ end of the crRNA portion each comprise a 2′-O-methyl chemical modification.
In an embodiment, a plurality of the nucleotides at positions 11-14, 17-18, and 25-26 from the 5′ end of the crRNA portion each comprise a 2′-fluoro chemical modification.
In an embodiment, a plurality of the nucleotides at positions 1-11, 14, 16-17, 19-22, 25, 29 and 33-67 from the 5′ end of the tracrRNA portion each comprise a 2′-O-methyl chemical modification.
In an embodiment, a plurality of the nucleotides at positions 18, 23-24, and 27-28 from the 5′ end of the tracrRNA portion each comprise a 2′-fluoro chemical modification.
In an embodiment, a plurality of the nucleotides at positions 11-19 and 22-26 from the 5′ end of the crRNA portion each comprise a 2′-fluoro chemical modification.
In an embodiment, a plurality of the nucleotides at positions 12-13, 15,18, 23-24, 27-28, and 30-32 from the 5′ end of the tracrRNA portion each comprise a 2′-fluoro chemical modification.
In an embodiment, a guide RNA modification pattern is selected from the group consisting of:
mN#mN#mN#mNmNmNmNmNmNmNrNrNrNrNrNmNmNmNrNm NmGrUrUrUmUmAmGmAmGmCmUmAmU#mG#mCmU (crRNA 1);
mN#mN#mN#mNmNmNmNmNmNmNrNrNrNrNrNrNmNmNrNmN mGrUrUrUrUrAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 7);
mN#mN#mN#mNmNmNmNmNmNmNrNrNrNrNrNrNrNrNrNmNm GrUrUrUmUmAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 8);
mN#mN#mN#mNmNmNmNmNmNmNrNrNrNrNrN#rN#rNrNrN#m NmGrU#rU#rU#mUmAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 9);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#mUmAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 10);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#rN#rN#rN#mNmGrU#rU#rU#mUmAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 11);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#mUrA#mGmAmGmCmUmAmU#mG#mC#mU (crRNA 17);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#rU#mAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 18);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#rU#rA#mGmAmGmCmUmAmU#mG#mC#mU (crRNA 19);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#fUfAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 20);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNfNfNfNfNfNmNm GfUfUfUfUfAmGmAmGmCmUmAmU#mG#mC#Mu (crRNA 21);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGfUrU#fUfUfAmGmAmGmCmUmAmU#mG#mC#mU (crRNA 22);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 2);
mA#mG#mC#mAmUmAmGmCmAmAmGrU#rU#mArA#mAmArU#mAmAmGmGrC#rU#mArG#rU#rC#mCrG#rU#rU#mAmUmCmAmAmCmUmUm GmAmAmAmAmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGm C#mU#mU#mU (tracrRNA 3);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmAmAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 4);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmAfUmA mAmGmGfCfUmArGfUfCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 6);
mA#mG#mC#mAmUmAmGmCmAmAmGrUfUmArAmAmAfUmA mAmGmGfCfUmAfGfUfCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 7);
mA#mG#mC#mAmUmAmGmCmAmAmGfUfUmAfAmAmAfUmA mAmGmGfCfUmAfGfUfCmCfGfUfUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 8);
mA#mG#mC#mAmUmAmGmCmAmAmGfUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 9);
mA#mG#mC#mAmUmAmGmCmAmAmGrUfUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 10);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmAfAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 11);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmAfUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 12);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGfCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 13);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCfUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 14);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmAfGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 15);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGfUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 16);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUfCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 17);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCfGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 18);
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGfUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 19); and
mA#mG#mC#mAmUmAmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUfUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (tracrRNA 20), wherein rN=RNA, mN=2′-O-methyl RNA, fN=2′-fluoro RNA, N#N=phosphorothioate linkage, and N=any nucleotide.
In an embodiment, the chemically modified guide RNA further comprises at least one moiety conjugated to the guide RNA.
In an embodiment, the at least one moiety is conjugated to at least one of the 5′ end of the crRNA portion, the 3′ end of the crRNA portion, the 5′ end of the tracrRNA portion, and the 3′ end of the tracrRNA portion.
In an embodiment, the at least one moiety increases cellular uptake of the guide RNA.
In an embodiment, the at least one moiety promotes specific tissue distribution of the guide RNA.
In an embodiment, the at least one moiety is selected from the group consisting of fatty acids, steroids, secosteroids, lipids, gangliosides analogs, nucleoside analogs, endocannabinoids, vitamins, receptor ligands, peptides, aptamers, and alkyl chains.
In an embodiment, the at least one moiety is selected from the group consisting of cholesterol, docosahexaenoic acid (DHA), docosanoic acid (DCA), lithocholic acid (LA), GalNAc, amphiphilic block copolymer (ABC), hydrophilic block copolymer (HBC), poloxamer, Cy5, and Cy3.
In an embodiment, the at least one moiety is conjugated to the guide RNA via a linker.
In an embodiment, the linker is selected from the group consisting of an ethylene glycol chain, an alkyl chain, a polypeptide, a polysaccharide, and a block copolymer.
In an embodiment, the at least one moiety is a modified lipid.
In an embodiment, the modified lipid is a branched lipid. In an embodiment, the modified lipid is a branched lipid of Formula I, Formula I: X-MC(=Y)M-Z-[L-MC(=Y)M-R]n, where X is a moiety that links the lipid to the guide RNA, each Y is independently oxygen or sulfur, each M is independently CH2, NH, 0 or S, Z is a branching group which allows two or three (“n”) chains to be joined to a chemically modified guide RNA, L is an optional linker moiety, and each R is independently a saturated, monounsaturated or polyunsaturated linear or branched moiety from 2 to 30 atoms in length, a sterol, or other hydrophobic group.
In an embodiment, the modified lipid is a headgroup-modified lipid. In an embodiment, the modified lipid is a headgroup-modified lipid of Formula II, Formula II: X-MC(=Y)M-Z-[L-MC(=Y)M-R]n-L-K-J, where X is a moiety that links the lipid to the guide RNA, each Y is independently oxygen or sulfur, each M is independently CH2, NH, N-alkyl, 0 or S, Z is a branching group which allows two or three (“n”) chains to be joined to chemically modified guide RNA, each L is independently an optional linker moiety, and R is a saturated, monounsaturated or polyunsaturated linear or branched moiety from 2 to 30 atoms in length, a sterol, or other hydrophobic group, K is a phosphate, sulfate, or amide and J is an aminoalkane or quaternary aminoalkane group.
In an embodiment, the guide RNA binds to a Cas9 nuclease selected from the group consisting of S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9).
In an embodiment, the Cas9 is a variant Cas9 with altered activity.
In an embodiment, the variant Cas9 is selected from the group consisting of a Cas9 nickase (nCas9), a catalytically dead Cas9 (dCas9), a hyper accurate Cas9 (HypaCas9), a high fidelity Cas9 (Cas9-HF), an enhanced specificity Cas9 (eCas9), and an expanded PAM Cas9 (xCas9).
In an embodiment, the Cas9 off-target activity is reduced relative to an unmodified guide RNA.
In an embodiment, the Cas9 on-target activity is increased relative to an unmodified guide RNA.
In an embodiment, the chemically modified guide RNA further comprises a nucleotide or non-nucleotide loop or linker linking the 3′ end of the crRNA portion to the 5′ end of the tracrRNA portion.
In an embodiment, the non-nucleotide linker comprises an ethylene glycol oligomer linker.
In an embodiment, the nucleotide loop is chemically modified.
In certain aspects, the disclosure provides a modified guide RNA comprising: (a) a crRNA portion comprising (i) a guide sequence capable of hybridizing to a target polynucleotide sequence, and (ii) a repeat sequence; and (b) a tracrRNA portion comprising an anti-repeat nucleotide sequence that is complementary to the repeat sequence, wherein the repeat sequence of the crRNA portion and the anti-repeat sequence on the tracrRNA are modified to increase binding affinity between the repeat sequence and the anti-repeat sequence relative to an unmodified guide RNA.
In an embodiment, the modified guide RNA comprises an increased GC nucleotide content in the repeat and anti-repeat region relative to an unmodified guide RNA.
In an embodiment, the modified guide RNA comprises ribose modifications in the repeat and anti-repeat region.
In an embodiment, the repeat and anti-repeat modifications enhance the stability of pairing between the crRNA portion and the tracrRNA portion.
In an embodiment, the crRNA portion comprises the guide RNA modification pattern of NNNNNNNNNNNNNNNNNNNNGUUUUAGAGCGAGCGC and the tracrRNA portion comprises the guide RNA modification pattern of GCGCUCGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGU GGCACCGAGUCGGUGCUUU, wherein N=any nucleotide.
In an embodiment, the one or more nucleotides are chemically modified.
In an embodiment, each one or more chemically modified nucleotides independently comprise a modification of a ribose group, a modification of a phosphate group, a modification of a nucleobase, or a combination thereof.
In an embodiment, each modification of the ribose group is independently selected from the group consisting of 2′-O-methyl, 2′-fluoro, 2′-deoxy, 2′-O-(2-methoxyethyl) (MOE), 2′-NH2, or a bicyclic nucleotide such as locked nucleic acid (LNA), 2′-(S)-constrained ethyl (S-cEt), constrained MOE, or 2′-0,4′-C-aminomethylene bridged nucleic acid (2′,4′-BNANC).
In an embodiment, each modification of the phosphate group is independently selected from the group consisting of a phosphorothioate, phosphonoacetate (PACE), thiophosphonoacetate (thioPACE), amide, triazole, phosphonate, or phosphotriester modification.
In an embodiment, each modification of the nucleobase group is independently selected from the group consisting of 2-thiouridine, 4-thiouridine, N6-methyladenosine, pseudouridine, 2,6-diaminopurine, inosine, thymidine, 5-methylcytosine, 5-substituted pyrimidine, isoguanine, isocytosine, or halogenated aromatic groups.
In an embodiment, the modified guide RNA comprises a combination of increased GC nucleotide content in the repeat and anti-repeat region relative to an unmodified guide RNA and one or more chemically modified nucleotides.
In an embodiment, the modified guide RNA comprises a modification pattern selected from the group consisting of:
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#fUfAmGmAmGmCmGmAmG#mC#mG#mC (hiGC crRNA 1);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#fUfAmGmAfGfCfGfAfG#fC#mG#mC (hiGC crRNA 2);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NmGrU#rU#rU#fUfAmGmAfGmCfGmAfG#mC#mG#mC (hiGC crRNA 3);
mN#mN#mN#mNmNmNmNmNmNmNfNfNfNfNrN#rN#fNfNrN#m NfGrU#rU#rU#fUfAmGmAfGmCfGmAfG#mC#mG#mC (hiGC crRNA 4);
mG#mC#mG#mCmUmCmGmCmAmAmGrUrUmArAmAmArUmA mAmGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAm AmAmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#m U (hiGC tracrRNA 1);
mG#mC#fG#fCfUfCfGfCmAmAmGrUrUmArAmAmArUmAmAmG mGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAmAmAm GmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#mU (hiGC tracrRNA 2);
mG#mC#fG#mCfUmCfGmCmAmAmGrUrUmArAmAmArUmAmA mGmGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAmAm AmGmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#mU (hiGC tracrRNA 3); and
mG#mC#fG#mCfUmCfGmCmAmAmGrUrUfArAfAfArUmAmAmG mGrCrUmArGrUrCmCrGrUrUmAmUmCmAmAmCmUmUmGmAmAmAmAmAm GmUmGmGmCmAmCmCmGmAmGmUmCmGmGmUmGmC#mU#mU#mU (hiGC tracrRNA 4), wherein rN=RNA, mN=2′-O-methyl RNA, fN=2′-fluoro RNA, N#N=phosphorothioate linkage, and N=any nucleotide.
In certain aspects, the disclosure provides a method of altering expression of a target gene in a cell, comprising administering to said cell a genome editing system comprising: a chemically modified guide RNA comprising: (a) a crRNA portion comprising (i) a guide sequence capable of hybridizing to a target polynucleotide sequence, and (ii) a repeat sequence; and (b) a tracrRNA portion an anti-repeat nucleotide sequence that is complementary to the repeat sequence; and an RNA-guided nuclease or a polynucleotide encoding an RNA-guided nuclease, wherein the chemically modified guide RNA comprises at least 80% modified nucleotides.
In an embodiment, the expression of the target gene is knocked out or knocked down.
In an embodiment, the sequence of the target gene is modified, edited, corrected or enhanced.
In an embodiment, the guide RNA and the RNA-guided nuclease comprise a ribonucleoprotein (RNP) complex.
In an embodiment, the RNA-guided nuclease is selected from the group consisting of S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9).
In an embodiment, the Cas9 is a variant Cas9 with altered activity.
In an embodiment, the variant Cas9 is selected from the group consisting of a Cas9 nickase (nCas9), a catalytically dead Cas9 (dCas9), a hyper accurate Cas9 (HypaCas9), a high fidelity Cas9 (Cas9-HF), an enhanced specificity Cas9 (eCas9), and an expanded PAM Cas9 (xCas9).
In an embodiment, the polynucleotide encoding an RNA-guided nuclease comprises a vector.
In an embodiment, the vector is a viral vector.
In an embodiment, the viral vector is an adeno-associated virus (AAV) vector or a lentivirus (LV) vector.
In an embodiment, the polynucleotide encoding an RNA-guided nuclease comprises a synthetic mRNA.
In certain aspects, the disclosure provides a CRISPR genome editing system comprising, a chemically modified guide RNA comprising: (a) a crRNA portion comprising (i) a guide sequence capable of hybridizing to a target polynucleotide sequence, and (ii) a repeat sequence; and (b) a tracrRNA portion comprising an anti-repeat nucleotide sequence that is complementary to the repeat sequence; and an RNA-guided nuclease or a polynucleotide encoding an RNA-guided nuclease, wherein the chemically modified guide RNA comprises at least 80% modified nucleotides.
In an embodiment, the one or more modified nucleotides comprise a modification in a ribose group, a phosphate group, a nucleobase, or a combination thereof.
In an embodiment, at least 80% of the ribose groups are chemically modified.
In an embodiment, each modification of the ribose group is independently selected from the group consisting of 2′-O-methyl, 2′-fluoro, 2′-deoxy, 2′-O-(2-methoxyethyl) (MOE), 2′-NH2, a bicyclic nucleotide, a locked nucleic acid (LNA), a 2′-(S)-constrained ethyl (S-cEt), a constrained MOE, or a 2′-0,4′-C-aminomethylene bridged nucleic acid (2′,4′-BNANN).
In an embodiment, each modification of the phosphate group is independently selected from the group consisting of a phosphorothioate, phosphonoacetate (PACE), thiophosphonoacetate (thioPACE), amide, triazole, phosphonate, or phosphotriester modification.
In an embodiment, each modification of the nucleobase group is independently selected from the group consisting of 2-thiouridine, 4-thiouridine, N6-methyladenosine, pseudouridine, 2,6-diaminopurine, inosine, thymidine, 5-methylcytosine, 5-substituted pyrimidine, isoguanine, isocytosine, or halogenated aromatic groups.
In an embodiment, the guide RNA comprises at least 90% modified nucleotides.
In an embodiment, the guide RNA comprises 100% modified nucleotides.
In an embodiment, the RNA-guided nuclease is selected from the group consisting of S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9).
In an embodiment, the Cas9 is a variant Cas9 with altered activity.
In an embodiment, the variant Cas9 is selected from the group consisting of a Cas9 nickase (nCas9), a catalytically dead Cas9 (dCas9), a hyper accurate Cas9 (HypaCas9), a high fidelity Cas9 (Cas9-HF), an enhanced specificity Cas9 (eCas9), and an expanded PAM Cas9 (xCas9).
In an embodiment, the Cas9 off-target activity is reduced relative to an unmodified guide RNA.
In an embodiment, the Cas9 on-target activity is increased relative to an unmodified guide RNA.
In certain aspects, the disclosure provides a chemically modified guide RNA comprising: (a) a crRNA portion comprising (i) a guide sequence capable of hybridizing to a target polynucleotide sequence, and (ii) a repeat sequence; and (b) a tracrRNA portion comprising an anti-repeat nucleotide sequence that is complementary to the repeat sequence, wherein the chemically modified guide RNA comprises at least 100% modified nucleotides.
In an embodiment, all ribose groups are chemically modified.
The foregoing and other features and advantages of the present disclosure will be more fully understood from the following detailed description of illustrative embodiments taken in conjunction with the accompanying drawings. The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
DNA cleavage assays were performed using saturating (8 pmols) and sub-saturating (0.8 pmols) amounts of Cas9 RNP complex. The ctrl refers to an unmodified crRNA:tracrRNA pair.
Provided herewith are novel chemically modified crRNAs and tracrRNAs, including heavily or fully chemically modified crRNAs and tracrRNAs. In certain embodiments, crRNAs and tracrRNAs with 5′ and/or 3′ conjugated moieties are provided. In yet other embodiments, crRNAs and tracrRNAs with modifications in the repeat region of the crRNA or the anti-repeat region of the tracrRNA are provided. Methods of using the crRNAs and tracrRNAs of the disclosure for genome editing with a CRISPR nuclease and kits for performing the same are also provided.
Unless otherwise defined herein, nomenclature used in connection with cell and tissue culture, molecular biology, immunology, microbiology, genetics and protein and nucleic acid chemistry and hybridization described herein are those well-known and commonly used in the art. The methods and techniques provided herein are usually performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification unless otherwise indicated. Enzymatic reactions and purification techniques are performed according to manufacturer's specifications unless otherwise specified, as commonly accomplished in the art or as described herein. The nomenclature used in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art, unless otherwise specified. Standard techniques are used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of patients.
Unless otherwise defined herein, scientific and technical terms used herein have the meanings that are commonly understood by those of ordinary skill in the art. In the event of any latent ambiguity, definitions provided herein take precedent over any dictionary or extrinsic definition. Unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. The use of “or” means “and/or” unless stated otherwise. The use of the term “including,” as well as other forms, such as “includes” and “included,” is not limiting.
So that the disclosure may be more readily understood, certain terms are first defined.
As used herein, the term “guide RNA” or “gRNA” refer to any nucleic acid that promotes the specific association (or “targeting”) of an RNA-guided nuclease such as a Cas9 to a target sequence (e.g., a genomic or episomal sequence) in a cell.
As used herein, a “modular” or “dual RNA” guide comprises more than one, and typically two, separate RNA molecules, such as a CRISPR RNA (crRNA) and a trans-activating crRNA (tracrRNA), which are usually associated with one another, for example by duplexing. gRNAs and their component parts are described throughout the literature (see, e.g., Briner et al. Mol. Cell, 56(2), 333-339 (2014), which is incorporated by reference).
As used herein, a “unimolecular gRNA,” “chimeric gRNA,” or “single guide RNA (sgRNA)” comprises a single RNA molecule. The sgRNA may be a crRNA and tracrRNA linked together. For example, the 3′ end of the crRNA may be linked to the 5′ end of the tracrRNA. A crRNA and a tracrRNA may be joined into a single unimolecular or chimeric gRNA, for example, by means of a four nucleotide (e.g., GAAA) “tetraloop” or “linker” sequence bridging complementary regions of the crRNA (at its 3′ end) and the tracrRNA (at its 5′ end).
As used herein, a “repeat” sequence or region is a nucleotide sequence at or near the 3′ end of the crRNA which is complementary to an anti-repeat sequence of a tracrRNA.
As used herein, an “anti-repeat” sequence or region is a nucleotide sequence at or near the 5′ end of the tracrRNA which is complementary to the repeat sequence of a crRNA.
Additional details regarding guide RNA structure and function, including the gRNA/Cas9 complex for genome editing may be found in, at least, Mali et al. Science, 339(6121), 823-826 (2013); Jiang et al. Nat. Biotechnol. 31(3). 233-239 (2013); and Jinek et al. Science, 337(6096), 816-821 (2012); which are incorporated by reference herein.
As used herein, a “guide sequence” or “targeting sequence” refers to the nucleotide sequence of a gRNA, whether unimolecular or modular, that is fully or partially complementary to a target domain or target polynucleotide within a DNA sequence in the genome of a cell where editing is desired. Guide sequences are typically 10-30 nucleotides in length, preferably 16-24 nucleotides in length (for example, 16, 17, 18, 19, 20, 21, 22, 23 or 24 nucleotides in length), and are at or near the 5′ terminus of a Cas9 gRNA.
As used herein, a “target domain” or target polynucleotide sequence” is the DNA sequence in a genome of a cell that is complementary to the guide sequence of the gRNA.
In addition to the targeting domains, gRNAs typically include a plurality of domains that influence the formation or activity of gRNA/Cas9 complexes. For example, as mentioned above, the duplexed structure formed by first and secondary complementarity domains of a gRNA (also referred to as a repeat: anti-repeat duplex) interacts with the recognition (REC) lobe of Cas9 and may mediate the formation of Cas9/gRNA complexes (Nishimasu et al. Cell 156: 935-949 (2014); Nishimasu et al. Cell 162(2), 1113-1126 (2015), both incorporated by reference herein). It should be noted that the first and/or second complementarity domains can contain one or more poly-A tracts, which can be recognized by RNA polymerases as a termination signal. The sequence of the first and second complementarity domains are, therefore, optionally modified to eliminate these tracts and promote the complete in vitro transcription of gRNAs, for example through the use of A-G swaps as described in Briner 2014, or A-U swaps. These and other similar modifications to the first and second complementarity domains are within the scope of the present disclosure.
Along with the first and second complementarity domains, Cas9 gRNAs typically include two or more additional duplexed regions that are necessary for nuclease activity in vivo but not necessarily in vitro (Nishimasu 2015, supra). A first stem-loop near the 3′ portion of the second complementarity domain is referred to variously as the “proximal domain,” “stem loop 1” (Nishimasu 2014, supra; Nishimasu 2015, supra) and the “nexus” (Briner 2014, supra). One or more additional stem loop structures are generally present near the 3′ end of the gRNA, with the number varying by species: S. pyogenes gRNAs typically include two 3′ stem loops (for a total of four stem loop structures including the repeat: anti-repeat duplex), while s. aureus and other species have only one (for a total of three). A description of conserved stem loop structures (and gRNA structures more generally) organized by species is provided in Briner 2014, which is incorporated herein by reference. Additional details regarding guide RNAs generally may be found in WO2018026976A1, which is incorporated herein by reference.
A representative guide RNA is shown in
Chemically Modified Guide RNA
The chemically modified guide RNAs of the disclosure possess improved in vivo stability, improved genome editing efficacy, and/or reduced immunotoxicity relative to unmodified or minimally modified guide RNAs.
Chemically modified guide RNAs of the disclosure contain one or more modified nucleotides comprising a modification in a ribose group, a phosphate group, a nucleobase, or a combination thereof.
Chemical modifications to the ribose group may include, but are not limited to, 2′-O-methyl, 2′-fluoro, 2′-deoxy, 2′-O-(2-methoxyethyl) (MOE), 2′-NH2, 2′-O-Allyl, 2′-O-Ethylamine, 2′-O-Cyanoethyl, 2′-O-Acetalester, or a bicyclic nucleotide such as locked nucleic acid (LNA), 2′-(S)-constrained ethyl (S-cEt), constrained MOE, or 2′-0,4′-C-aminomethylene bridged nucleic acid (2′,4′-BNANC).
Chemical modifications to the phosphate group may include, but are not limited to, a phosphorothioate, phosphonoacetate (PACE), thiophosphonoacetate (thioPACE), amide, triazole, phosphonate, or phosphotriester modification.
Chemical modifications to the nucleobase may include, but are not limited to, 2-thiouridine, 4-thiouridine, N6-methyladenosine, pseudouridine, 2,6-diaminopurine, inosine, thymidine, 5-methylcytosine, 5-substituted pyrimidine, isoguanine, isocytosine, or halogenated aromatic groups.
The chemically modified guide RNAs may have one or more chemical modifications in the crRNA portion and/or the tracrRNA portion for a modular or dual RNA guide. The chemically modified guide RNAs may also have one or more chemical modifications in the single guide RNA for the unimolecular guide RNA.
The chemically modified guide RNAs may comprise at least about 50% to at least about 100% chemically modified nucleotides, at least about 60% to at least about 100% chemically modified nucleotides, at least about 70% to at least about 100% chemically modified nucleotides, at least about 80% to at least about 100% chemically modified nucleotides, at least about 90% to at least about 100% chemically modified nucleotides, and at least about 95% to at least about 100% chemically modified nucleotides.
The chemically modified guide RNAs may comprise at least about 50% chemically modified nucleotides, at least about 60% chemically modified nucleotides, at least about 70% chemically modified nucleotides, at least about 80% chemically modified nucleotides, at least about 90% chemically modified nucleotides, at least about 95% chemically modified nucleotides, at least about 99% chemically modified, or 100% (fully) chemically modified nucleotides.
The chemically modified guide RNAs may comprise at least about 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% chemically modified nucleotides.
Guide RNAs that comprise at least about 80% chemically modified nucleotides to at least about 99% chemically modified nucleotides are considered “heavily” modified, as used herein.
Guide RNAs that comprise 100% chemically modified nucleotides are considered “fully” modified, as used herein.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified ribose group at about 50% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, and at about 95% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified ribose group at about 50% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides, at about 95% of the guide RNA nucleotides, at about 99% of the guide RNA nucleotides, or at 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified ribose group at about 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% of the guide RNA nucleotides.
Guide RNAs that have at least about 80% of the ribose groups chemically modified to at least about 99% of the ribose groups chemically modified are considered “heavily” modified, as used herein.
Guide RNAs that have 100% of the ribose groups chemically modified are considered “fully” modified, as used herein.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified phosphate group at about 50% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, and at about 95% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified phosphate group at about 50% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides, at about 95% of the guide RNA nucleotides, at about 99% of the guide RNA nucleotides, or at 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified phosphate group at about 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% of the guide RNA nucleotides.
Guide RNAs that have at least about 80% of the phosphate groups chemically modified to at least about 99% of the phosphate groups chemically modified are considered “heavily” modified, as used herein.
Guide RNAs that have 100% of the phosphate groups chemically modified are considered “fully” modified, as used herein.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified nucleobase at about 50% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, and at about 95% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified nucleobase at about 50% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides, at about 95% of the guide RNA nucleotides, at about 99% of the guide RNA nucleotides, or at 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise a chemically modified nucleobase at about 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% of the guide RNA nucleotides.
Guide RNAs that have at least about 80% of the nucleobases chemically modified to at least about 99% of the nucleobases chemically modified are considered “heavily” modified, as used herein.
Guide RNAs that have 100% of the nucleobases chemically modified are considered “fully” modified, as used herein.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise any combination of chemically modified ribose groups, chemically modified phosphate groups, and chemically modified nucleobases at about 50% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides, and at about 95% of the guide RNA nucleotides to about 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise any combination of chemically modified ribose groups, chemically modified phosphate groups, and chemically modified nucleobases at about 50% of the guide RNA nucleotides, at about 60% of the guide RNA nucleotides, at about 70% of the guide RNA nucleotides, at about 80% of the guide RNA nucleotides, at about 90% of the guide RNA nucleotides, at about 95% of the guide RNA nucleotides, at about 99% of the guide RNA nucleotides, or at 100% of the guide RNA nucleotides.
In certain exemplary embodiments, the chemically modified guide RNAs may comprise any combination of chemically modified ribose groups, chemically modified phosphate groups, and chemically modified nucleobases at about 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% of the guide RNA nucleotides.
Guide RNAs that have at least about 80% of any combination of the ribose groups, the phosphate groups, and the nucleobases chemically modified to at least about 99% of the nucleobases chemically modified are considered “heavily” modified, as used herein.
Guide RNAs that have 100% of any combination of the ribose groups, the phosphate groups, and the nucleobases chemically modified are considered “fully” modified, as used herein.
The heavily and fully chemically modified guide RNAs of the disclosure possess several advantages over the minimally modified guide RNAs in the art. Heavily and fully chemically modified guide RNAs are expected to ease chemical synthesis, further enhance in vivo stability, and provide a scaffold for terminally appended chemical functionalities that facilitate delivery and efficacy during clinical applications to genome editing.
The chemical modification pattern used in the guide RNA is preferably such that activity of the guide RNA is maintained when paired with an RNA-guided DNA endonuclease, e.g., Cas9. Exemplary chemical modification patterns are described in Table 1 below.
It will be understood to those of skill in the art that the base sequence of the first 20 nucleotides of the exemplary crRNAs recited in Table 1 above are directed to a specific target. This 20 nucleotide base sequence may be changed based on the target nucleic acid, however the chemical modifications remain the same.
It will be further understood to those of skill in the art that the guide sequence may be 10-30 nucleotides in length, preferably 16-24 nucleotides in length (for example, 16, 17, 18, 19, 20, 21, 22, 23 or 24 nucleotides in length), and is at or near the 5′ terminus of a Cas9 gRNA.
High-Affinity Repeat/Anti-Repeat Guide RNA Modifications
A crRNA and a tracrRNA hybridize together by forming a duplex between the repeat region of the crRNA and the anti-repeat region of the tracrRNA (see
The high-affinity interaction may be enhanced by increasing the GC nucleotide content in the duplex formed by the repeat regions and the anti-repeat region. Nucleotide modifications, such as 2′-Fluoro and 2′-O-Methyl modifications, may also be introduced, which increase the melting temperature (Tm) of the duplex. Further modifications include the use of orthogonal and non-naturally occurring nucleotides. The various repeat region/anti-repeat region modifications described herein enhance the stability of the duplex, helping to prevent the crRNA and tracrRNA from folding into sub-optimal structures and therefore promoting higher genome editing efficacy.
The use of a modular, or dual RNA, guide RNA approach over a single guide RNA (sgRNA) approach has several advantages, including the ease of making the shorter crRNA and tracrRNA relative to a longer sgRNA, and the reduced cost of manufacturing the dual RNAs relative to the sgRNA. Exemplary crRNAs and tracrRNAs with modifications in the repeat and anti-repeat region, including a high GC content and 2′-Fluoro modifications, are shown in Table 2 and Table 3 below, and at
Guide RNA Conjugates
The chemically modified guide RNAs of the disclosure may be modified with terminally conjugated moieties. As used herein, a “terminally conjugated moiety” or “moiety” refers to a compound which may be linked or attached to the 5′ and/or 3′ end of the crRNA and/or tracrRNA of a guide RNA. Terminally conjugated moieties can provide increased stability, increased ability to penetrate cell membranes, increase cellular uptake, increase circulation time in vivo, act as a cell-specific directing reagent, and/or provide a means to monitor cellular or tissue-specific uptake.
Terminally conjugated moieties may be conjugated on the 5′ end and/or the 3′ end of a crRNA and/or a tracrRNA, as, for example, in
In certain exemplary embodiments, a terminally conjugated moiety includes, but is not limited to, fatty acid, steroid, secosteroid, lipid, ganglioside analog, nucleoside analogs, endocannabinoid, vitamin, receptor ligand, peptide, aptamer, alkyl chain, fluorophore, antibody, nuclear localization signal, and the like.
In certain exemplary embodiments, a terminally conjugated moiety includes, but is not limited to, cholesterol, cholesterol-triethylene glycol (TEGChol), docosahexaenoic acid (DHA), docosanoic acid (DCA), lithocholic acid (LA), GalNAc, amphiphilic block copolymer (ABC), hydrophilic block copolymer (HBC), poloxamer, Cy5, Cy3, and the like.
In certain exemplary embodiments, the at least one terminally conjugated moiety is a modified lipid, including a branched lipid (such as the structure shown in Formula I) or a headgroup-modified lipid (such as the structure shown in Formula II).
X-MC(=Y)M-Z-[L-MC(=Y)M-R]n Formula I:
where X is a moiety that links the lipid to the guide RNA, each Y is independently oxygen or sulfur, each M is independently CH2, NH, O or S, Z is a branching group which allows two or three (“n”) chains to be joined to the rest of the structure, L is an optional linker moiety, and each R is independently a saturated, monounsaturated or polyunsaturated linear or branched moiety from 2 to 30 atoms in length, a sterol, or other hydrophobic group.
X-MC(=Y)M-Z-[L-MC(=Y)M-R]n-L-K-J Formula II:
where X is a moiety that links the lipid to the guide RNA, each Y is independently oxygen or sulfur, each M is independently CH2, NH, N-alkyl, O or S, Z is a branching group which allows two or three (“n”) chains to be joined to the rest of the structure, each L is independently an optional linker moiety, and R is a saturated, monounsaturated or polyunsaturated linear or branched moiety from 2 to 30 atoms in length, a sterol, or other hydrophobic group, K is a phosphate, sulfate, or amide and J is an aminoalkane or quaternary aminoalkane group.
The moieties may be attached to the terminal nucleotides of the guide RNA via a linker. Exemplary linkers include, but are not limited to, an ethylene glycol chain, an alkyl chain, a polypeptide, a polysaccharide, a block copolymer, and the like.
Exemplary crRNAs and tracrRNAs with conjugated moieties may be found in Table 4 below.
Where: Chol—cholesterol; GalNAc—(N-Acetylgalactosamine) 3-40 moieties; DHA Docosahexaenoic Acid; DCA—Docosanoic Acid; LA—lithocholic Acid; ABC—Amphiphilic block copolymer (PK modifier); HBC—Hydrophilic block copolymer (PK modifier); and Pol—poloxamers (PK modifier).
Chemically Modified Single Guide RNA
As described herein, the chemically modified guide RNAs of the disclosure may be constructed as single guide RNAs (sgRNAs) by linking the 3′ end of a crRNA to the 5′ end of a tracrRNA. The linker may be an oligonucleotide loop, including a chemically modified oligonucleotide loop. The linker may be a non-nucleotide chemical linker, including, but not limited to, ethylene glycol oligomers (see, e.g., Pils et al. Nucleic Acids Res. 28(9): 1859-1863 (2000)).
RNA-Guided Nucleases
RNA-guided nucleases according to the present disclosure include, without limitation, naturally-occurring Type II CRISPR nucleases such as Cas9, as well as other nucleases derived or obtained therefrom. Exemplary Cas9 nucleases that may be used in the present disclosure include, but are not limited to, S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9). In functional terms, RNA-guided nucleases are defined as those nucleases that: (a) interact with (e.g., complex with) a gRNA; and (b) together with the gRNA, associate with, and optionally cleave or modify, a target region of a DNA that includes (i) a sequence complementary to the targeting domain of the gRNA and, optionally, (ii) an additional sequence referred to as a “protospacer adjacent motif;” or “PAM,” which is described in greater detail below. As the following examples will illustrate, RNA-guided nucleases can be defined, in broad terms, by their PAM specificity and cleavage activity, even though variations may exist between individual RNA-guided nucleases that share the same PAM specificity or cleavage activity. Skilled artisans will appreciate that some aspects of the present disclosure relate to systems, methods and compositions that can be implemented using any suitable RNA-guided nuclease having a certain PAM specificity and/or cleavage activity. For this reason, unless otherwise specified, the term RNA-guided nuclease should be understood as a generic term, and not limited to any particular type (e.g., Cas9 vs. Cpfl), species (e.g., S. pyogenes vs. S. aureus) or variation (e.g., full-length vs. truncated or split; naturally-occurring PAM specificity vs. engineered PAM specificity).
Various RNA-guided nucleases may require different sequential relationships between PAMs and protospacers. In general, Cas9s recognize PAM sequences that are 5′ of the protospacer as visualized relative to the top or complementary strand.
In addition to recognizing specific sequential orientations of PAMs and protospacers, RNA-guided nucleases generally recognize specific PAM sequences. S. aureus Cas9, for example, recognizes a PAM sequence of NNGRRT, wherein the N sequences are immediately 3′ of the region recognized by the gRNA targeting domain. S. pyogenes Cas9 recognizes NGG PAM sequences. It should also be noted that engineered RNA-guided nucleases can have PAM specificities that differ from the PAM specificities of similar nucleases (such as the naturally occurring variant from which an RNA-guided nuclease is derived, or the naturally occurring variant having the greatest amino acid sequence homology to an engineered RNA-guided nuclease). Modified Cas9s that recognize alternate PAM sequences are described below.
RNA-guided nucleases are also characterized by their DNA cleavage activity: naturally-occurring RNA-guided nucleases typically form DSBs in target nucleic acids, but engineered variants have been produced that generate only SSBs (discussed above; see also Ran 2013, incorporated by reference herein), or that do not cut at all.
The RNA-guided nuclease Cas9 may be a variant of Cas9 with altered activity. Exemplary variant Cas9 nucleases include, but are not limited to, a Cas9 nickase (nCas9), a catalytically dead Cas9 (dCas9), a hyper accurate Cas9 (HypaCas9) (Chen et al. Nature, 550(7676), 407-410 (2017)), a high fidelity Cas9 (Cas9-HF) (Kleinstiver et al. Nature 529(7587), 490-495 (2016)), an enhanced specificity Cas9 (eCas9) (Slaymaker et al. Science 351(6268), 84-88 (2016)), and an expanded PAM Cas9 (xCas9) (Hu et al. Nature doi: 10.1038/nature26155 (2018)).
The RNA-guided nucleases may be combined with the chemically modified guide RNAs of the present disclosure to form a genome-editing system. The RNA-guided nucleases may be combined with the chemically modified guide RNAs to form an RNP complex that may be delivered to a cell where genome-editing is desired. The RNA-guided nucleases may be expressed in a cell where genome-editing is desired with the chemically modified guide RNAs delivered separately. For example, the RNA-guided nucleases may be expressed from a polynucleotide such as a vector or a synthetic mRNA. The vector may be a viral vector, including, be not limited to, an adeno-associated virus (AAV) vector or a lentivirus (LV) vector.
It will be readily apparent to those skilled in the art that other suitable modifications and adaptations of the methods described herein may be made using suitable equivalents without departing from the scope of the embodiments disclosed herein. Having now described certain embodiments in detail, the same will be more clearly understood by reference to the following examples, which are included for purposes of illustration only and are not intended to be limiting.
crRNAs and tracrRNAs were synthesized at 1 μmole scale on an Applied Biosystems 394 DNA synthesizer. BTT (0.25 M in acetonitrile, ChemGenes) was used as activator. 0.05 M iodine in pyridine:water (9:1) (TEDIA) was used as oxidizer. DDTT (0.1 M, ChemGenes) was used as sulfurizing agent. 3% TCA in DCM (TEDIA) was used as deblock solution. RNAs were grown on 1000 Å CPG functionalized with Unylinker (˜42 μmol/g). RNA and 2′-OMe phosphoramidites (ChemGenes) were dissolved in acetonitrile to 0.15 M; the coupling time was 10 min for each base. The nucleobases were deprotected with a 3:1 NH4OH:EtOH solution for 48 hours at room temperature. Deprotection of the TBDMS group was achieved with DMSO:NEt3.3HF (4:1) solution (500 μL) at 65° C. for 3 hours. RNA oligonucleotides were then recovered by precipitation in 3M NaOAc (25 μL) and n-BuOH (1 mL), and the pellet was washed with cold 70% EtOH and resuspended in 1 mL RNase-free water.
Purification of the crRNAs and tracrRNAs were carried out by high performance liquid chromatography using a 1260 infinity system with an Agilent PL-SAX 1000 Å column (150×7.5 mm, 8 μm). Buffer A: 30% acetonitrile in water; Buffer B: 30% acetonitrile in 1M NaClO4 (aq). Excess salt was removed with a Sephadex Nap-10 column.
crRNAs and tracrRNAs were analyzed on an Agilent 6530 Q-TOF LC/MS system with electrospray ionization and time of flight ion separation in negative ionization mode. The data were analyzed using Agilent Mass Hunter software. Buffer A: 100 mM hexafluoroisopropanol with 9 mM triethylamine in water; Buffer B: 100 mM hexafluoroisopropanol with 9 mM trimethylamine in methanol.
crRNA and tracrRNA were extensively modified while retaining the efficacy of SpyCas9-based genome editing in cultured human cells. Structure-guided and systematic approaches were used to introduce 2′-OMe-RNA, 2′-F-RNA and PS modifications throughout guide RNAs (Table 5 and Table 6). The strategy described herein yielded active RNP complexes with both extensively and fully modified versions of crRNAs and tracrRNAs.
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Crystal structures of SpyCas9 have been solved as the RNP alone or bound to one or both strands of target DNA (Nishimasu et al. Cell 156: 935-949 (2014); Anders al. Nature 513: 569 (2014); Jiang et al. Science 351: 867-871 (2016); Jiang et al, Science 348: 1477-1481 (2015)). These structures provide detailed information regarding the interactions between the Cas9 protein and the crRNA:tracrRNA complex. These structures were used to identify sites where Cas9 protein makes no contacts with the crRNA or tracrRNA.
Chemically Modified crRNA and tracrRNA Screening Methods
Cell Culture
Screening was performed in a HEK293T stable cell line expressing the traffic light reporter (TLR) system. The HEK293T cells were cultured in Dulbecco-modified Eagle's Minimum Essential Medium (DMEM; Life Technologies). DMEM was also supplemented with 10% Fetal Bovine Serum (FBS; Sigma). Cells were grown in a humidified 37° C., 5% CO2 incubator.
Expression and Purification of Spy-Cas9
The pMCSG7 vector expressing the Cas9 from Streptococcus pyogenes was used. In this construct, the Cas9 also contains three nuclear localization signals (NLSs). Rosetta DE3 strain of Escherichia coli was transformed with the 3×NLS-SpyCas9 construct. For expression and purification of 3×NLS-SpyCas9, a previously described protocol was used (Jinek et al. Science, 337: 816 (2012)). The bacterial culture was grown at 37° C. until an OD600 of 0.6 was reached. Then, the bacterial culture was cooled to 18° C., and 1 mM Isopropyl 13-D-1-thiogalactopyranoside (IPTG; Sigma) was added to induce protein expression. Cells were grown overnight for 16-20 hours.
The bacterial cells were harvested and resuspended in Lysis Buffer [50 mM Tris-HCl (pH 8.0), 5 mM imidazole]. 10 μg/mL of Lysozyme (Sigma) was then added to the mixture and incubated for 30 minutes at 4° C. This was followed by the addition of 1×HALT Protease Inhibitor Cocktail (ThermoFisher). The bacterial cells were then sonicated and centrifuged for 30 minutes at 18,000 rpm. The supernatant was then subjected to Nickel affinity chromatography. The elution fractions containing the SpyCas9 were then further purified using cation exchange chromatography using a 5 mL HiTrap S HP column (GE). This was followed by a final round of purification by size-exclusion chromatography using a Superdex-200 column (GE). The purified protein was concentrated and flash frozen for subsequent use.
Transfection of HEK293T Cells
The HEK293T cells were nucleofected using the Neon transfection system (ThermoFisher) according to the manufacturer's protocol. Briefly, 20 picomoles of 3×NLS-SpyCas9 was mixed with 25 picomoles of crRNA:tracrRNA in buffer R (ThermoFisher) and incubated at room temperature for 20-30 minutes. This Cas9 RNP complex was then mixed with approximately 100,000 cells which were already resuspended in buffer R. This mixture was nucleofected with a 10 μL Neon tip and then plated in 24-well plates containing 500 μL of DMEM and 10% FBS. The cells were stored in a humidified 37° C. and 5% CO2 incubator for 2-3 days.
Flow Cytometry Analysis
The nucleofected HEK293T cells were analyzed on MACSQuant® VYB from Miltenyi Biotec. For mCherry detection, the yellow laser (561 nm) was used for excitation and 615/20 nm filter used to detect emission. At least 20,000 events were recorded and the subsequent analysis was performed using FlowJo® v10.4.1. Cells were first sorted based on forward and side scattering (FSC-A vs SSC-A) to eliminate debris. Cells were then gated using FSC-A and FSC-H to select single cells. Finally, mCherry signal was used to select for mCherry-expressing cells. The percent of cells expressing mCherry was calculated and reported in this application as a measure of Cas9-based genome editing.
Indel Analysis by TIDE
The genomic DNA from HEK293T cells was harvested using DNeasy Blood and Tissue kit (Qiagen) as recommended by the manufacturer. Approximately 50 ng of genomic DNA was used to PCR-amplify a ˜700 base pair fragment that was subsequently purified using a QIAquick PCR Purification kit (Qiagen). The PCR fragment was then sequenced by Sanger sequencing and the trace files were subjected to indel analysis using the TIDE web tool (Brinkman et al. Nucleic Acids Research, 42: e168 (2014)). Results are reported as % Indel rate.
In Vitro DNA Cleavage Assays
The traffic light reporter plasmid (Addgene: 31482) was linearized with restriction enzyme EcoRI (N.E.B.) for 1 hour, 37° C. in NEB buffer 3, followed by heat inactivation for 20 minutes at 65° C. For the Cas9 digest, 200 ng of linearized plasmid DNA was added to pre-formed RNP complexes (8 pmol or 0.8 pmol) and incubated for 1 hour at 37° C. in 25 μl NEB buffer 3. Cut DNA was purified using Zymo DNA purification columns and separated on a 1% agarose gel run at 100 V. Relative intensities of full length and Cas9-cut DNA fragments were determined using Image J software.
Serum Stability Assays
A 10 μM Cas9 RNP complex was first assembled in cleavage buffer [20 mM HEPES (pH 7.5), 250 mM KCl and 10 mM MgCl2]. Then 2 μM Cas9 RNP was incubated with 8% FBS in a 50 μL reaction at 37° C. Then at time points of 0 hours, 1 hour and 20 hours, 10 μLs of the reaction mixture was treated with Proteinase K and then 10 μL of quench buffer (90% formamide and 25 mM EDTA) was added to the solution. The reaction mixture was resolved on a 10% denaturing polyacrylamide gel containing 6 M Urea. The gel was stained with SYBR Safe and visualized on Typhoon FLA imager.
Initial Screening
2′-OMe modifications were introduced at guide positions 7-10 and 20 (C2,
Chemically modified crRNAs C2 and C3 retain complete activity relative to the unmodified crRNA C0, suggesting that the modifications introduced in crRNAs C2 and C3 are well tolerated by Cas9 (
Screening of Further Optimized crRNAs
2′-OMe modifications were introduced into the first 6 nucleotides of C3 to yield C4 (
C4-C7 retain almost the same efficacy as C0, but C8 activity was strongly reduced. These results indicated that nucleotides at positions 1-6 and 17-18 tolerate 2′-OH substitutions. 2′-OMe modifications at positions 25 and 26 were tolerated in C6 but not in C8. A version of C8 that contained PS linkages at several unprotected positions including 15-16, 19 and 21-23 (C9) was also synthesized. This design also exhibited reduced editing efficiency by Cas9 (
2′-F-RNAs were also incorporated in this round of optimization since they can increase thermal and nuclease stability of RNA:RNA or RNA:DNA duplexes, and they also interfere minimally with C3′-endo sugar puckering (Patra et al. Angewandte Chemie International Edition 51: 11863-11866 (2012); Manoharan et al. Angewandte Chemie International Edition 50: 2284-2288 (2011)). 2′-F may be better tolerated than 2′-OMe at positions where the 2′-OH is important for RNA:DNA duplex stability. For these reasons, two crRNAs were synthesized based on C9 but with 2′-F modifications at positions 11-14 and/or 17-18 (C10-C11). These modifications rescued some of C9's diminished activity. In fact, C10 (which contained 2′-F substitutions at positions 11-14 and 17-18) performed better than C11, in which positions 17-18 were unmodified. The results suggest that 2′-F substitutions can compensate for lost efficacy resulting from high 2′-OMe content. It is especially noteworthy that C10 retains the same activity as the unmodified C0 but contains at least one backbone modification at every single phosphodiester linkage. This represents a significant breakthrough for Cas9-based therapeutics because C10 has great potential to provide increased stability, and therefore more efficient editing, in vivo.
Screening of Further Optimized tracrRNAs
T1 was further modified by introducing 2′-OMe substitutions at most positions where the 2′—OH groups do not make crystal contacts with the protein. In addition, some nucleotides that interact with Cas9 were also modified, given that the crRNA tolerated substitutions at many such positions. This approach produced tracrRNAs T2-T5, which contain modifications in at least 55 out of 67 nucleotides. The nucleotide at position 15 (A15) is the only position that differs between T2 and T4 whereas T3 contains additional stabilizing PS linkages at unprotected positions relative to T2. These tracrRNAs were tested in HEK293T-TLR cells, and the majority of 2′-OMe chemical modifications were tolerated by the tracrRNA except at position A15 (
The mCherry signal only results from indels producing a +1 frameshift, and therefore underestimates true editing efficiencies. To ensure that crRNA:tracrRNA combinations do not yield false negatives by favoring TLR indels that are out of the mCherry reading frame, Tracking of Indels by Decomposition (TIDE) analysis was also performed to analyze overall editing efficiencies. As shown in
Screening of Further Optimized crRNA:tracrRNA Pairs
Chemically modified C10 and T2 were further modified to attempt to define combined crRNA:tracrRNA modification patterns that are compatible with SpyCas9 RNP function. Because crRNA 2′-F substitutions were largely tolerated (
When C17-C22 were used with either T2 or the T0 control (20 pmol RNP), all showed comparable efficacy as the C0 and C10 crRNAs (
Among T6-T8, the best-performing tracrRNA was T6, especially with modified crRNAs including C20. The fully-modified tracrRNA (T8) compromised the potency of all crRNAs tested, but retains some function (˜5% editing with 20 pmol RNP) with C19 and C20 (
To verify that the crRNA designs of the disclosure are compatible with different guide sequences, including those targeting endogenous human genes, the C10 design was tested by targeting exon 50 of the huntingtin (HTT) gene (
Additional endogenous targets with several different modification patterns were test. Specifically, the genes HBB, HTT, and VEGFA were targeted with the C20 and C21 modification pattern, paired with the T2 and T8 modified tracrRNA (
These results demonstrate that the modified crRNA and tracrRNA designs are also applicable to endogenous target sites.
It has previously been shown that crRNA and tracrRNA can be fused with a GAAA tetraloop to yield a single guide RNA (sgRNA) with enhanced efficacy. Given the possibility that repeat:anti-repeat interactions could affect efficacy, the pairing between the repeat and anti-repeat of crRNA and tracrRNA was explored. Modifications were made to the repeat and anti-repeat regions, including increasing the GC nucleotide content and using 2′-Fluoro modifications. Repeat/Anti-Repeat modified crRNAs (hiGC C1-C4) and tracrRNAs (hiGC T1-T4) were designed to improve pairing between crRNA and tracrRNA (Table 5). All of the modified RNAs outperformed in vitro-transcribed sgRNA as well as synthetic, unmodified dual RNAs (
Terminally (5′ or 3′ end) conjugated moieties such as fluorophores, N-Acetylgalactosamine (GalNAc), or Cholesterol-Triethylene glycol (TEGChol) were added to the crRNAs and the tracrRNAs to determine if the terminally conjugated moieties could be tolerated. Such modifications can be useful for microscopy, and for monitoring cellular or tissue-specific RNA uptake. 5′-Cy3 modifications were introduced on crRNAs C10 and C11 to yield C12 and C13, respectively (Table 5). TegChol or GalNAc was also covalently attached to the 3′ end of C12 or C13 to obtain C14 and C15, respectively. Most crRNA conjugated moieties were tolerated on both ends, though some loss of function was observed with C13, C14 and C16 (
Terminally conjugated moieties may be placed on the 5′ end, the 3′ end, or both ends of a crRNA or tracrRNA as depicted in
The terminally conjugated moieties may be used to increase cellular uptake of the RNAs. The conjugates may also be used to promote specific tissue distribution of the RNAs.
The terminally conjugated moieties may be selected from fatty acids, steroids, secosteroids, lipids, gangliosides and nucleoside analogs, endocannabinoids, vitamins, receptor ligands, peptides, aptamers, alkyl chains, fluorophores, antibodies, and nuclear localization signals.
The terminally conjugated moieties may be selected from cholesterol, docosahexaenoic acid (DHA), docosanoic acid (DCA), lithocholic acid (LA), GalNAc, amphiphilic block copolymer (ABC), hydrophilic block copolymer (HBC), poloxamer, Cy5, and Cy3.
The tracrRNA T2 described above is heavily modified but still contains 12 unmodified (ribose) residues. The tracrRNA T8 described above replaces those 12 unmodified residues with 2′-Fluoro modifications to create a fully modified tracrRNA. Although both T2 and T8 are functional, T2 possess higher activity, indicating that one or more of the 12 2′-Fluoro modifications in T8, relative to T2, is causing the reduced activity in T8. In an effort to determine the one or more sites at which the 2′-Fluoro modification is deleterious, individual ribose residues from T2 where changed to 2′-Fluoro, one at a time. These 12 tracrRNAs (T9-T20) are shown in Table 1 above. T9-T20 were used with crRNAs C0, C20, C21 described above. The same HEK293T traffic light reporter (TLR) system was used as described above. As demonstrated in
This application claims priority to U.S. Provisional Patent Application No. 62/644,944, which was filed Mar. 19, 2018, the contents of which is incorporated herein in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2019/022818 | 3/18/2019 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62644944 | Mar 2018 | US |
