Compositions and methods for modification of biomolecules
The present invention provides modified cycloalkyne compounds; and method of use of such compounds in modifying biomolecules. The present invention features a cycloaddition reaction that can be carried out under physiological conditions. In general, the invention involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide 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:
wherein Y is H; a moiety that comprises a reactive group that facilitates covalent attachment of a molecule of interest; or a molecule of interest;
wherein R 1 is selected from 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, and a nitro,
wherein R 1 can be at any position on the cyclooctyne group other than at the two carbons linked by the triple bond, and other than the fluoride-substituted carbon.
2. The compound of claim 1 , wherein Y is a reactive group that facilitates covalent attachment of a molecule.
3. The compound of claim 2 , wherein the reactive group is selected from a carboxyl, an amine, an ester, a thioester, a sulfonyl halide, an alcohol, a thiol, a succinimidyl ester, an isothiocyanate, an iodoacetamide, a maleimide, and a hydrazine.
4. The compound of claim 1 , wherein Y is a molecule of interest selected from a detectable label, a toxin, a linker, a peptide, a drug, a member of a specific binding pair, and an epitope tag.
5. The compound of claim 1 , wherein the compound is of the structure:
6. A compound of the structure:
wherein R 8 is selected from H; a halogen atom; an aliphatic group, a substituted or unsubstituted alkyl group; an alkenyl group; an alkynyl group; a carboxylic acid, an alkyl ester; an aryl ester; a substituted aryl ester; an aldehyde; an amine; a thiol; 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; and a nitro.
7. A compound of the structure of one of Formulas XI-XVI:
wherein R, R 1 , R 2 , and R 3 are each independently H; a carboxylic acid; a methoxy; an alkyl ester; an aryl ester; a substituted aryl ester; an aldehyde; an amine; a thiol; 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; —W—(CH 2 ) n —Z (wherein n is an integer from 1-4, wherein W, if present, is O, N, or S; and Z is nitro, cyano, sulfonic acid, or a halogen); —(CH 2 ) n —W—(CH 2 ) m —Z (wherein n and m are each independently 1 or 2; W is O, N, S, or sulfonyl, wherein if W is O, N, or S, then Z is nitro, cyano, or halogen, and wherein and if W is sulfonyl, then Z is H); or —(CH 2 ) n —Z (wherein n is an integer from 1-4, and wherein Z is nitro, cyano, sulfonic acid, or a halogen); and;
wherein each R, R 1 , R 2 , and R 3 is optionally independently linked to a moiety that comprises a reactive group that facilitates covalent attachment of a molecule of interest; or a molecule of interest.
8. The compound of claim 7 , wherein:
R and R 2 are independently selected from —COCH 2 CH 2 CO 2 H and —CO-phenyl-CO 2 H.
9. The compound of claim 7 , wherein the compound is of one of the following structures: