Chemically Modified Guide RNAs for CRISPR/CAS-Mediated Gene Correction

Patent metadata

Field	Value
Publication number	US-2024401034-A1
Application number	US-202418408504-A
Country	US
Kind code	A1
Filing date	Jan 9, 2024
Priority date	Apr 6, 2015
Publication date	Dec 5, 2024
Grant date	—

Abstract

Provided herein are methods for inducing CRISPR/Cas-based gene regulation (e.g., genome editing or gene expression) of a target nucleic acid (e.g., target DNA or target RNA) in a cell. The methods include using modified single guide RNAs (sgRNAs) that enhance gene regulation of the target nucleic acid in a primary cell for use in ex vivo therapy or in a cell in a subject for use in in vivo therapy. Additionally, provided herein are methods for preventing or treating a genetic disease in a subject by administering a sufficient amount of a modified sgRNA to correct a mutation in a target gene associated with the genetic disease.

First claim

1 - 50 . (canceled)

51 . A composition comprising:
(a) a primary cell; (b) a modified single guide RNA (sgRNA) comprising a first nucleotide sequence that is complementary to a target nucleic acid within the primary cell and a second nucleotide sequence that interacts with a CRISPR-associated protein (Cas) polypeptide, wherein: (i) about 10% to about 30% of nucleotides in the first nucleotide sequence and/or about 1% to about 10% of nucleotides in the second nucleotide sequence are modified nucleotides; (ii) the modified sgRNA comprises a modified nucleotide within five nucleotides from the 5′ end of the first nucleotide sequence and/or within five nucleotides from the 3′ end of the second nucleotide sequence; and (iii) the modified nucleotides are selected from the group consisting of a 2′-O-methyl 3′-phosphorothioate (MS) nucleotide, a 2′-O-methyl 3′-thioPACE (MSP) nucleotide, and a combination thereof; and (c) a Cas polypeptide, an mRNA encoding the Cas polypeptide, or a recombinant expression vector comprising a nucleotide sequence encoding the Cas polypeptide, wherein the modified sgRNA guides the Cas polypeptide to the target nucleic acid, and wherein the modified sgRNA induces a gene regulation of the target nucleic acid with an enhanced activity relative to a corresponding unmodified sgRNA; and (d) an electroporation agent.

52 . The composition of claim 51 , wherein the enhanced activity comprises increased stability of the modified sgRNA and/or increased specificity of the modified sgRNA for the target nucleic acid.

53 . The composition of claim 51 , wherein the target nucleic acid comprises a target DNA or a target RNA.

54 . The composition of claim 53 , wherein the gene regulation comprises genome editing of the target DNA.

55 . The composition of claim 54 , wherein the genome editing comprises homologous-directed repair (HDR) or nonhomologous end joining (NHEJ) of the target DNA.

56 . The composition of claim 54 , further comprising a recombinant donor repair template.

57 . The composition of claim 56 , wherein the recombinant donor repair template comprises two nucleotide sequences comprising two non-overlapping, homologous portions, wherein one of the two homologous portions is located at the 5′ end and the other homologous portion is located at the 3′ end of the recombinant donor template, wherein each homologous portion is homologous to a corresponding region of the target DNA to undergo genome editing.

58 . The composition of claim 56 , wherein the recombinant donor repair template comprises a synthetic single-stranded oligodeoxynucleotide (ssODN) template comprising a nucleotide sequence encoding a mutation to correct a single nucleotide polymorphism (SNP) and two nucleotide sequences comprising two non-overlapping, homologous portions that are homologous to corresponding regions of the target DNA, wherein one of the two homologous portions is located at the 5′ end and the other homologous portion is located at the 3′ end of the recombinant donor template.

59 . The composition of claim 53 , wherein the Cas polypeptide is endonuclease-deficient.

60 . The composition of claim 51 , wherein the primary cell is isolated from a multicellular organism.

61 . The composition of claim 60 , wherein the multicellular organism is a plant, a multicellular protist, a multicellular fungus, or an animal.

62 . The composition of claim 51 , wherein the primary cell is a stem cell or an immune cell.

63 . The composition of claim 62 , wherein the stem cell is a hematopoietic stem cell, a hematopoietic progenitor cell, a mesenchymal stem cell, a neural stem cell, or an organ stem cell.

64 . The composition of claim 62 , wherein the immune cell is a T cell, a natural killer cell, a monocyte, a peripheral blood mononuclear cell (PBMC), or a peripheral blood lymphocyte (PBL).

65 . The composition of claim 51 comprising a population of primary cells.

66 . The composition of claim 65 , wherein the modified sgRNA induces the gene regulation of the target nucleic acid in at least about 30% of the population of primary cells.

67 . The composition of claim 51 , wherein the first nucleotide sequence is about 20 nucleotides in length.

68 . The composition of claim 51 , wherein at least two nucleotides in the first nucleotide sequence are modified nucleotides.

69 . The composition of claim 51 , wherein one or more modified nucleotides are located within five nucleotides from the 5′-end of the first nucleotide sequence.

70 . The composition of claim 51 , wherein from about 10% to about 30% of the nucleotides in the first nucleotide sequence are modified nucleotides.

71 . The composition of claim 51 , wherein the second nucleotide sequence is about 80 nucleotides in length.

72 . The composition of claim 51 , wherein at least two nucleotides in the second nucleotide sequence are modified nucleotides.

73 . The composition of claim 51 , wherein one or more modified nucleotides are located within five nucleotides from the 3′-end of the second nucleotide sequence.

74 . The composition of claim 51 , wherein from about 1% to about 10% of the nucleotides in the second nucleotide sequence are modified nucleotides.

75 . The composition of claim 51 , wherein the modified sgRNA comprises one, two, or three consecutive or non-consecutive modified nucleotides at or near the 5′-end of the first nucleotide sequence and one, two, or three consecutive or non-consecutive modified nucleotides at or near the 3′-end of the second nucleotide sequence.

76 . The composition of claim 75 , wherein the modified sgRNA comprises three consecutive modified nucleotides at the 5′-end of the first nucleotide sequence and three consecutive modified nucleotides at the 3′-end of the second nucleotide sequence.

77 . The composition of claim 51 , wherein the primary cell comprises mRNA encoding the Cas polypeptide.

78 . The composition of claim 51 , wherein the Cas polypeptide is a Cas9 polypeptide, a variant thereof, or a fragment thereof.

79 . The composition of claim 51 , wherein the Cas polypeptide is a nickase.

80 . The composition of claim 51 , wherein the modified sgRNA and the Cas polypeptide are formed in a ribonucleoprotein (RNP) complex,
wherein the modified sgRNA guides the Cas polypeptide to the target nucleic acid, and wherein the modified sgRNA induces a gene regulation of the target nucleic acid with an enhanced activity relative to a corresponding unmodified sgRNA.

81 . The composition of claim 51 , wherein the primary cell is a primary CD34 + hematopoietic stem or progenitor cell.

82 . The composition of claim 81 , wherein the primary CD34 + hematopoietic stem or progenitor cell comprises a mutation in the HBB gene responsible for sickle cell anemia.

83 . The composition of claim 81 , wherein the primary CD34 + hematopoietic stem or progenitor cell comprises a mutation in the HBB gene responsible for thalassemia.

84 . The composition of claim 81 , further comprising a recombinant donor repair template.

85 . The composition of claim 84 , wherein the recombinant donor repair template comprises two nucleotide sequences comprising two non-overlapping, homologous portions, wherein

Assignees

• Univ Leland Stanford Junior
• Agilent Technologies Inc

Inventors

• Porteus Matthew H
• Hendel Ayal
• Clark Joe
• Bak Rasmus O
• Ryan Daniel E
• Dellinger Douglas J
• Kaiser Robert
• Myerson Joel

Classifications

• C12N15/907

  in mammalian cells · CPC title

• C12N9/96

  Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates · CPC title

• C12N2310/10

  Type of nucleic acid · CPC title

• C12N2310/531

  Stem-loop; Hairpin · CPC title

• C12N15/111

  General methods applicable to biologically active non-coding nucleic acids · CPC title