Engineered chimeric pegylated ADI and methods of use
Provided are chimeric arginine deiminases, including pegylated chimeric arginine deiminases, and related compositions and methods of use thereof, including methods of treating cancer.
1. A recombinant chimeric arginine deiminase (ADI) comprising a catalytic domain of an ADI protein derived from a first microorganism and an α-helical domain of an ADI protein derived from a second microorganism, wherein the first microorganism differs from the second microorganism, wherein the recombinant chimeric ADI comprises that amino acid sequence set forth in any one of SEQ ID NOs: 55, 56, 35, 58, 34, or 59 or a variant having at least 98% identity to any one of SEQ ID NOs: 55, 56, 35, 58, 34, or 59, with or without the hexahistidine tag.
2. The recombinant chimeric ADI of claim 1 , wherein the recombinant chimeric ADI comprises the amino acid sequence set forth in any one of SEQ ID NOs: 55, 56, 35, 58, 34, or 59, with or without the hexahistidine tag.
3. The recombinant chimeric ADI of claim 1 , wherein the recombinant chimeric ADI has been modified to remove at least one pegylation site.
4. The recombinant chimeric ADI of claim 1 , wherein at least one lysine residue has been modified by an amino acid substitution.
5. The recombinant chimeric ADI of claim 1 covalently bonded via a biocompatible linker to polyethylene glycol (PEG).
6. The recombinant chimeric ADI of claim 5 , wherein the arginine deiminase is covalently bonded to more than one polyethylene glycol molecule.
7. The recombinant chimeric ADI of claim 5 , wherein the arginine deiminase is covalently bonded to about 1 to about 10 polyethylene glycol molecules.
8. The recombinant chimeric ADI of claim 5 , wherein the arginine deiminase is covalently bonded to 5±3 PEG molecules.
9. The recombinant chimeric ADI of claim 5 , wherein the PEG molecules are straight chain or branch chain PEG molecules.
10. The recombinant chimeric ADI of claim 5 , wherein the polyethylene glycol has a total weight average molecular weight of from about 1,000 to about 40,000.
11. The recombinant chimeric ADI of claim 4 , wherein the polyethylene glycol has a total weight average molecular weight of from about 10,000 to about 30,000.
12. The recombinant chimeric ADI of claim 5 , wherein the biocompatible linker comprises a succinyl group, an amide group, an imide group, a carbamate group, an ester group, an epoxy group, a carboxyl group, a hydroxyl group, a carbohydrate, a tyrosine group, a cysteine group, a histidine group, a methylene group, or a combination thereof.
13. The recombinant chimeric ADI of claim 12 , wherein the source of the succinyl group is succinimidyl succinate.
14. A polynucleotide encoding the recombinant chimeric ADI of claim 1 .
15. A vector comprising the polynucleotide of claim 14 .
16. An isolated host cell comprising the vector of claim 15 .
17. A composition comprising the recombinant chimeric ADI of claim 1 and a physiologically acceptable carrier.
18. The composition of claim 17 , further comprising an autophagy modulator.
19. The composition of claim 18 , wherein the autophagy modulator is selected from the group consisting of chloroquine, 3-methyladenine, hydroxychloroquine, bafilomycin A1, 5-amino-4-imidazole carboxamide riboside (AICAR), okadaic acid, N6-mercaptopurine riboside, vinblastine, wortmannin, rapamycin, everolimus, metformin, perifosine, resveratrol, and tamoxifen.
20. The composition of claim 17 , further comprising a chemotherapeutic agent.
21. The composition of claim 20 wherein the chemotherapeutic agent is selected from the group consisting of docetaxel, carboplatin, cyclophosphamide, gemcitabine, cisplatin, sorafenib, sunitinib and everolimus.
22. A method of treating, ameliorating the symptoms of, or inhibiting the progression of a cancer comprising administering to a patient in need thereof a therapeutically effective amount of the composition of claim 17 , thereby treating, ameliorating the symptoms of, or inhibiting the progression of the cancer.
23. The method of claim 22 wherein the cancer is selected from the group consisting of melanoma, pancreatic cancer, prostate cancer, small cell lung cancer, mesothelioma, lymphocytic leukemia, chronic myelogenous leukemia, lymphoma, hepatoma, sarcoma, leukemia, acute myeloid leukemia, relapsed acute myeloid leukemia, breast cancer, ovarian cancer, colorectal cancer, gastric cancer, glioma, glioblastoma multiforme, non-small cell lung cancer (NSCLC), kidney cancer, bladder cancer, uterine cancer, esophageal cancer, brain cancer, head and neck cancers, cervical cancer, testicular cancer, and stomach cancer.