Engineered demeter 5-methylcytosine DNA glyosylase with improved yield, stability and solubility
View Patent ↗Improved active DEMETER polypeptides with internal deletions are provided.
1. An isolated polypeptide consisting of:
a first amino acid sequence, wherein the first amino acid sequence is at least 90% identical to the amino acid sequence of SEQ ID NO: 1,
a second amino acid sequence, wherein the second amino acid sequence is at least 90% identical to the amino acid sequence of SEQ ID NO: 2, and
optionally a linker, wherein the linker consists of 1-300 amino acids,
wherein the first and second amino acid sequences are linked directly or by the linker and wherein the polypeptide excises methylated cytosines in DNA when contacted to DNA comprising methylated cytosines.
2. The polypeptide of claim 1 , wherein the first and second amino acid sequences are linked directly.
3. The polypeptide of claim 1 , wherein the first and second amino acid sequences are linked by the linker.
4. The polypeptide of claim 3 , wherein the linker is heterologous to the first or second amino acid sequence.
5. The polypeptide of claim 3 , wherein the linker consists of 10-300 amino acids of the amino acid sequence of SEQ ID NO: 3.
6. The polypeptide of claim 3 , wherein the linker consists of 20 or fewer amino acids.
7. The polypeptide of claim 3 , wherein the linker consists of the amino acid sequence of SEQ ID NO: 4.
8. The polypeptide of claim 1 , wherein the first amino acid sequence is at least 95% identical to the amino acid sequence of SEQ ID NO: 1.
9. The polypeptide of claim 1 , wherein the second amino acid sequence is at least 95% identical to the amino acid sequence of SEQ ID NO: 2.
10. The polypeptide of claim 1 , wherein the first amino acid sequence consists of the amino acid sequence of SEQ ID NO: 1 and the second amino acid sequence consists of the amino acid sequence of SEQ ID NO: 2.
11. A method of making the polypeptide of claim 1 , the method comprising, culturing an isolated cell under conditions to allow for expression of the polypeptide of claim 1 , wherein the isolated cell comprises an expression cassette, the expression cassette comprising a promoter operably linked to a polynucleotide encoding the polypeptide of claim 1 thereby making the polypeptide of claim 1 .
12. The method of claim 11 , further comprising purifying the polypeptide.
13. The method of claim 11 , wherein the cell is a eukaryotic cell.
14. The method of claim 13 , wherein the cell is a yeast, fungal, mammalian or insect cell.
15. The method of claim 11 , wherein the cell is a prokaryotic cell.