Methods for generating analogs of coenzyme A
View Patent ↗Methods to generate analogs of coenzyme A in vitro and in vivo are disclosed. The methods comprise reacting pantetheine or a derivative thereof with a reporter to form labeled pantetheine or a derivative thereof, phosphorylating the labeled pantetheine or derivative thereof to form phosphopantetheine or a derivative thereof, adenylating the labeled phosphopantetheine or derivative thereof to form a labeled dephosphoCoenzyme A or derivative thereof, and phosphorylating the 3′-hydrozyl of the labeled dephosphoCoenzume A or derivative thereof to form a labeled coenzyme A analog or derivative thereof.
1. A method to generate analogs of coenzyme A, comprising:
phosphorylating a pantetheine analog or a derivative thereof to form a phosphopantetheine analog or a derivative thereof, the pantetheine analog or derivative thereof comprising a reporter or a bioorthogonal tag having reactivity with a reporter,
adenylating the phosphopantetheine analog or a derivative thereof to form a dephosphocoenzyme A analog or a derivative thereof, and,
phosphorylating the 3′-hydroxyl of the dephosphocoenzyme A analog or a derivative thereof to form a coenzyme A analog or a derivative thereof, wherein the phosphorylating of the pantetheine analog or a derivative thereof, the adenylating, or the phosphorylating the 3′-hydroxyl of the dephosphocoenzyme A analog or a derivative thereof is catalyzed by one or more native enzymes.
2. The method of claim 1 , wherein the pantetheine analog or derivative thereof comprises three modules.
3. The method of claim 2 , wherein the three modules are selected from a ω-functionalized amine, a sidechain, an α-amino acid, a β-amino acid, a linker, and a modulator.
4. The method of claim 3 , wherein the ω-functionalized amine, the sidechain, the α-amino acid, the β-amino acid, the linker, or the modulator comprises the reporter or the bioorthogonal tag.
5. The method of claim 3 , wherein the modulator is a dihydroxy acid, an aminohydroxy acid, a pantoic acid, or a homolog or derivative of pantoic acid.
6. The method of claim 1 , wherein the phosphorylation of the pantetheine analog or derivative thereof is catalyzed by a native enzyme.
7. The method of claim 6 , wherein the native enzyme is a kinase.
8. The method of claim 7 , wherein the kinase is a pantothenate kinase.
9. The method of claim 1 , wherein adenylating the phosphopantetheine analog or derivative thereof is catalyzed by a native enzyme.
10. The method of claim 9 , wherein the native enzyme is an adenylyltransferase.
11. The method of claim 10 , wherein the adenylyltransferase is phosphopantetheine adenylyltransferase.
12. The method of claim 1 , wherein phosphorylating the 3′-hydroxyl of the dephosphocoenzyme A analog or derivative thereof is catalyzed by a native enzyme.
13. The method of claim 12 , wherein the native enzyme is a kinase.
14. The method of claim 13 , wherein the kinase is a dephospho-CoA kinase.
15. The method of claim 1 , further comprising contacting the coenzyme A analog or derivative thereof with a carrier protein domain to form a reporter labeled protein.
16. The method of claim 15 , wherein the carrier protein domain comprises a fusion construct between a peptide or carrier protein domain and a protein of interest.
17. The method of claim 15 , wherein formation of the reporter labeled protein is catalyzed by a phosphotransferase.
18. The method of claim 17 , wherein the phosphotransferase is 4′-phosphopantetheinyltransferase.
19. The method of claim 1 , wherein the phosphopantetheine analog or derivative thereof can be used to detect proteins, identify proteins, characterize proteins, inhibit proteins, activate proteins, or examine the structure of proteins.
20. The method of claim 1 , wherein the dephosphocoenzyme A analog or derivative thereof can be used to detect proteins, identify proteins, characterize proteins, inhibit proteins, activate proteins, or examine the structure of proteins.
21. The method of claim 1 , wherein the coenzyme A analog or derivative thereof can be used to detect proteins, identify proteins, characterize proteins, inhibit proteins, activate proteins, or examine the structure of proteins.
22. The method of claim 1 , further comprising contacting the bioorthogonal tag with a reporter, the reporter and the bioorthogonal tag forming a covalent attachment.
23. The method of claim 22 , wherein the reporter is attached to the bioorthogonal tag by an azide-alkyne cycloaddition reaction.
24. The method of claim 22 , wherein the reporter is attached to the bioorthogonal tag by a ketone-hydroxylamine reaction.
25. The method of claim 22 , wherein the reporter is an affinity reporter, a colored reporter, a fluorescent reporter, a magnetic reporter, a radioisotopic reporter, a peptide reporter, a metal reporter, a nucleic acid reporter, a lipid reporter, a glycosylation reporter, a reactive reporter, an enzyme inhibitor, or a biomolecular substrate.
26. The method of claim 1 , wherein the reporter is a fluorescent reporter.
27. The method of claim 1 , wherein the reporter is a precursor to a fluorescent reporter.