ARGININE MODIFICATION AND CONJUGATION METHODS
Provided herein are methods for modifying an arginine residue to provide a reactive handle suitable for attaching the arginine residue to a label, linker, or other target molecule. The methods utilize an Arnold Salt to convert the guanidine group of the arginine residue into a formylpyrimidine, and are efficient and very selective. Provided herein are mild reaction conditions for this arginine modification, making it suitable for use with complex biomolecules like proteins. The methods can include one or more additional steps to attach the modified arginine to a linker for further manipulation or for connecting the arginine residue to a target compound. Provided methods are especially useful for covalently linking an arginine-containing peptide to a target molecule such as a polynucleotide.
1 . A method to functionalize a guanidine on the side chain of an amino acid residue, wherein the method comprises contacting the amino acid residue with an Arnold Salt under conditions that result in formation of a formyl-substituted pyrimidine of Formula (I):
wherein:
X represents the remainder of the side chain of the amino acid residue, and
each R is independently selected from methyl, ethyl, and propyl, or two R on the same N can optionally be taken together with the nitrogen to which they are attached to form a 4-6 membered ring.
2 . The method of claim 1 , wherein the amino acid residue is an arginine in a peptide.
3 . The method of claim 1 , wherein the arginine residue is contacted with the Arnold Salt in a medium comprising an aqueous buffer and further comprising an organic cosolvent.
4 . The method of claim 1 , wherein the arginine residue is contacted with the Arnold Salt in a medium at a temperature between 40° C. and 80° C.
5 . The method of claim 4 , wherein the medium has a pH between 8 and 12.
6 . The method of claim 1 , wherein at least 50% of the arginine residue in a sample is modified to form the formyl pyrimidine of Formula (I).
7 . The method of claim 1 , wherein the Arnold Salt is associated with a counterion selected from Br 3 − , ClO 4 − , PF 6 − , and BF 4 − .
8 . The method of claim 2 , wherein the peptide is joined to a solid support.
9 . The method of claim 1 , which further comprises a step of contacting the formyl pyrimidine of Formula (I) with a compound that comprises a target molecule and an aldehyde-reactive reaction handle having an —NH 2 group, to form a conjugate of the formula:
wherein X represents the alkyl portion of the side chain of an arginine residue,
L 1 represents a linker, and
Tm represents the target molecule.
10 . The method of claim 9 , wherein the conjugate is of the formula:
wherein X represents the alkyl portion of the side chain of the arginine residue,
Y is O or NH,
L 2 represents a linker; and
Tm represents the target molecule.
11 . The method of claim 10 , wherein the method further comprises a step of contacting the conjugate with a reducing agent to provide a conjugate of the formula:
wherein X represents the alkyl portion of the side chain of the arginine residue,
Y is O or NH, and
Tm represents the target molecule.
12 . The method of claim 9 , wherein X represents a peptide connected to the remainder of the conjugate through the alkyl portion of the side chain of an arginine residue of the peptide.
13 . The method of claim 12 , wherein Tm represents a polynucleotide.
14 . A modified amino acid residue comprising a substructure of Formula (I):
wherein X represents the side chain portion of the amino acid residue.
15 . The modified arginine residue of claim 14 , wherein the amino acid residue is an arginine in a peptide.
16 . The modified arginine residue of claim 15 , wherein the peptide is joined to a solid support.
17 . A conjugate comprising the structure:
wherein X represents a side chain of an amino acid residue,
L 2 is a linker;
Y is selected from a bond, O and NH; and
Tm′ represents a target molecule.
18 . The conjugate of claim 17 , wherein X represents the side chain of an arginine residue in a peptide.
19 . The conjugate of claim 18 , wherein the peptide is joined to a solid support.
20 . The conjugate of claim 18 , wherein Y is —O— or —NH—.
21 . A method of attaching a peptide comprising at least one arginine residue to a target molecule, the method comprising the steps of:
(a) contacting the at least one arginine residue with an Arnold Salt under conditions that result in formation of a formyl-substituted pyrimidine of Formula (I):
wherein:
X represents the peptide connected through the at least one arginine residue, and each R is independently selected from methyl, ethyl, and propyl, or two R on the same N can optionally be taken together with the nitrogen to which they are attached to form a 4-6 membered ring; and
(b) contacting the formyl pyrimidine of Formula (I) with a compound that comprises the target molecule and an aldehyde-reactive reaction handle having an —NH 2 group, to form a conjugate of the formula:
wherein X represents the peptide connected through the at least one arginine residue, L 1 represents a linker, and Tm represents the target molecule.
22 . The method of claim 21 , wherein the target molecule comprises a polynucleotide.
23 . The method of claim 21 , wherein the conjugate is of the formula:
wherein X represents the alkyl portion of the side chain of the arginine residue,
Y is —O— or —NH—, L 2 represents a linker; and Tm represents the target molecule.