Use of specifically engineered enzymes to enhance the efficacy of prodrugs
View Patent ↗The invention provides methods for enhancing efficiency of prodrugs by specifically engineered enzymes with enhanced activity towards nucleoside analogs used in cancer chemotherapy, and delivering the enzymes to specific target cells in a patient. The invention also provides modified deoxycytidine kinase (dCK) mutants with such enhanced activity. Furthermore, the invention provides antibody-conjugated enzymes that can be specifically delivered to leukemic blast cells in vivo or ex vivo.
1. A modified human deoxycytidine kinase having the amino acid sequence identified by SEQ ID NO: 1, wherein amino acid residue 104 and amino acid residue 133 are substituted, and wherein the modified human deoxycytidine kinase is capable of phosphorylating wild type human deoxycytidine kinase substrates.
2. The modified human deoxycytidine kinase of claim 1 , wherein amino acid residue 104 is substituted with methionine.
3. The modified human deoxycytidine kinase of claim 1 , wherein amino acid residue 133 is substituted with alanine.
4. The modified human deoxycytidine kinase of claim 1 , wherein amino acid residue 104 is substituted with methionine, and amino acid residue 133 is substituted with alanine, and wherein the modified human deoxycytidine kinase has the amino acid sequence as identified by SEQ ID NO: 6.
5. The modified human deoxycytidine kinase of claim 1 wherein said modified human deoxycytidine kinase additionally phosphorylates thymidine or thymidine analogs.
6. A pharmaceutical composition comprising the modified human deoxycytidine kinase of claim 1 and a pharmaceutical acceptable carrier.
7. A pharmaceutical composition comprising the modified human deoxycytidine kinase of claim 2 and a pharmaceutically acceptable carrier.
8. A pharmaceutical composition comprising the modified human deoxycytidine kinase of claim 3 and a pharmaceutically acceptable carrier.
9. A pharmaceutical composition comprising the modified human deoxycytidine kinase of claim 4 and a pharmaceutically acceptable carrier.