Stapled peptides and method of synthesis
View Patent ↗A method for preparing stapled peptides. The stapled peptides, including helical stapled peptides, are prepared according to a photochemically-based method, a [3+2] cycloaddition reaction. The helical stapled peptides exhibit increased helicity, thermal stability and cell permeability.
1. A method for preparation of a stapled peptide, comprising the steps of:
a) providing a functionalized peptide, wherein the functionalized peptide comprises at least a first functionalized amino acid and a second functionalized amino acid, wherein the first functionalized amino acid comprises an alkene moiety and the second functionalized amino acid comprises a tetrazole moiety, wherein the second functionalized amino acid is the fourth or the seventh successive amino acid from the first functionalized amino acid, wherein the alkene and tetrazole moieties can react to form a pyrazoline moiety and the stapled peptide can exhibit helical secondary structure; and
b) exposing the functionalized peptide to electromagnetic radiation of a wavelength from 300 to 320 nm such that a stapled peptide having a pyrazoline moiety, formed from reaction of the alkene moiety with the tetrazole moiety, and exhibiting helical secondary structure is formed.
2. The method of claim 1 , wherein the functionalized peptide has a structure according to Formula I:
wherein,
R 1 is H or an alkyl group comprising 1 to 6 carbons,
R 2 is a phenyl group, a substituted phenyl group or a heterocyclic group,
R 3 is H or an alkyl group comprising 1 to 6 carbons,
R 4 is H or an alkyl group comprising 1 to 6 carbons,
X is a phenyl group, a substituted phenyl group, a heterocyclic group, or a direct linkage,
m is an integer from 1 to 6,
n is an integer from 1 to 6,
[Xaa] is any natural or synthetic amino acid,
x is an integer from 1 to 10,
y is 3 or 6, and
z is an integer from 1 to 10,
wherein the stapled peptide has a structure according to Formula II:
3. The method of claim 2 , wherein,
R 1 is H or methyl,
R 2 is a phenyl group or a substituted phenyl group selected from the group consisting of 4-methoxyphenyl group and N,N-dimethyl-4-aminophenyl group,
R 3 and R 4 are H,
X is a phenyl group or a direct linkage,
m and n are 3,
x and z are 1, and
y is 3.
4. The method of claim 1 , wherein the functionalized peptide is capable of forming an alpha-helix.
5. The method of claim 1 , wherein the alkene group is a methacrylate group and R 1 is H or a methyl group.