Genome editing enhancement
This invention pertains to single-stranded carrier nucleic acids and their methods of use for enhancing genome editing ribonucleoprotein complex transfection into cells and the resulting enhancement of CRISPR editing on the target DNA within those cells, as well as introduction of chemical modifications which reduce the integration of the single-stranded carrier nucleic acids at double-stranded breaks.
1. A carrier oligonucleotide to improve transfection of ribonucleoprotein (RNP) into a cell in a sample, wherein the carrier oligonucleotide is selected from SEQ ID Nos.: 4, 9, and 25.
2. The carrier oligonucleotide of claim 1 , wherein the carrier oligonucleotide is SEQ ID NO.: 4.
3. The carrier oligonucleotide of claim 1 , wherein the carrier oligonucleotide is SEQ ID NO.: 9.
4. The carrier oligonucleotide of claim 1 , wherein the carrier oligonucleotide is SEQ ID NO.: 25.
5. A method of improving transfection of a ribonucleoprotein into a cell of a sample, comprising:
contacting the cell of the sample with composition having a carrier oligonucleotide,
wherein the carrier oligonucleotide is selected from SEQ ID Nos.: 4, 9, and 25.
6. The method of claim 5 , wherein the concentration of the carrier oligonucleotide in the composition is at least 1 μM.
7. The method of claim 5 , wherein the carrier oligonucleotide is SEQ ID NO.: 4.
8. The method of claim 5 , wherein the carrier oligonucleotide is SEQ ID NO.: 9.
9. The method of claim 5 , wherein the carrier oligonucleotide is SEQ ID NO.: 25.
10. The method of claim 5 , wherein the ribonucleoprotein comprises a Cpf1 ribonucleoprotein.
11. The method of claim 10 , wherein the carrier oligonucleotide comprises SEQ ID No.: 4.
12. The method of claim 10 , wherein the carrier oligonucleotide comprises SEQ ID NO.: 9.
13. The method of claim 10 , wherein the carrier oligonucleotide comprises SEQ ID NO.: 25.