Chemoselective ligation
View Patent ↗The present invention features a chemoselective ligation reaction that can be carried out under physiological conditions. In general, the invention involves condensation of a specifically engineered phosphine, which can provide for formation of an amide bond between the two reactive partners resulting in a final product comprising a phosphine moiety, or which can be engineered to comprise a cleavable linker so that a substituent of the phosphine is transferred to the azide, releasing an oxidized phosphine byproduct and producing a native amide bond in the final product. The selectivity of the reaction and its compatibility with aqueous environments provides for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).
1. A compound of the formula:
where
R 1 is an alkyl ester, an aryl ester, a substituted aryl ester, an aldehyde, an amide, an aryl amide, an alkyl halide, a thioester, a sulfonyl ester, an alkyl ketone, an aryl ketone, a substituted aryl ketone, a halosulfonyl, a nitrile, or a nitro;
R 2 and R 3 are independently aryl groups, substituted aryl groups, or cycloalkyl groups; and
Y is selected from a dye, a drug, a cytotoxic molecule, a ligand for a receptor, a ligand-binding moiety, a receptor, and biotin.
2. The compound of claim 1 , wherein R 1 is a lower alkyl ester.
3. The compound of claim 2 , wherein the lower alkyl ester is a methyl ester.
4. The compound of claim 1 , wherein Y is a dye.
5. The compound of claim 1 , wherein Y is a drug.
6. The compound of claim 1 , wherein Y is a cytotoxic molecule.
7. The compound of claim 1 , wherein Y is a ligand for a receptor.
8. The compound of claim 1 , wherein Y is a ligand binding moiety.
9. The compound of claim 1 , wherein Y is a receptor.
10. The compound of claim 4 , wherein the dye is substantially undetectable until reaction of the compound with an azide.
11. The compound of claim 1 , wherein R 1 is a methyl ester, and wherein Y is biotin.
12. A compound of the formula:
where
R 1 is a carboxylic acid, an alkyl ester, an aryl ester, a substituted aryl ester, an aldehyde, an amide, an aryl amide, an alkyl halide, a thioester, a sulfonyl ester, an alkyl ketone, an aryl ketone, a substituted aryl ketone, a halosulfonyl, a nitrile, or a nitro;
R 2 and R 3 are independently aryl groups, substituted aryl groups, or cycloalkyl groups; and
Y is fluorescein, modified fluorescein, or an imaging agent.
13. The compound of claim 12 , wherein R 1 is a lower alkyl ester.
14. The compound of claim 12 , wherein the lower alkyl ester is a methyl ester.
15. The compound of claim 12 , wherein Y is fluorescein or modified fluorescein.
16. The compound of claim 12 , wherein Y is an imaging agent.
17. A compound of the formula:
where
R 1 is an alkyl ester, an aryl ester, a substituted aryl ester, an aldehyde,
an amide, an aryl amide, an alkyl halide, a thioester, a sulfonyl ester, an alkyl ketone, an aryl ketone, a substituted aryl ketone, a halosulfonyl, a nitrile, or a nitro;
R 2 and R 3 are independently aryl groups, substituted aryl groups, or cycloalkyl groups; and
Y is a carboxyl, an amine, an ester, a thioester, a sulfonyl halide, an alcohol, a thiol, a succinimidyl ester, isothiocyanate, iodoacetamide, maleimide, or hydrazine.
18. The compound of claim 17 , wherein R 1 is a lower alkyl ester.
19. The compound of claim 17 , wherein the lower alkyl ester is a methyl ester.