Polypeptide compositions formed using a coiled-coil template and methods of use
View Patent ↗The invention relates to the use of constrained coiled-coil polypeptides to mimic α-helical structural elements of native proteins. These constrained peptidyl mimetics are used to generate and/or identify ligands which selectively bind the α-helical segment contained in the native protein.
1. A method for stabilizing and displaying an epitope in a synthetic polypeptide comprising the formula (ab i c i de i f i g i ) n , where i=1,2, . . . , n, wherein n represents the number of heptad units, and n is at least three, said method comprising:
(a) selecting a solvent-accessible region of the epitope, wherein said region is not in a coiled-coil conformation in its native state, and inserting the amino acids from said region into the b i , c i , e i , f i and g i positions; and
(b) independently inserting an amino acid selected from the group consisting of leucine, isoleucine, valine, phenylalanine, methionine, tyrosine, and derivatives thereof, into each of the a and d positions such that the amino acids from the epitope in the b i , c i , e i , f i and g i positions are interrupted by the amino acids in the a and d positions, wherein (ab i c i de i f i g i ) n ,forms a coiled-coil.
2. The method of claim 1 wherein the amino acid at the a position is isoleucine, and the amino acid at the d position is leucine.
3. The method of claim 1 , wherein the polypeptide is comprised of two polypeptide chains arranged in a parallel configuration.
4. The method of claim 1 , wherein n is between about 3 and about 20.
5. The method of claim 1 , wherein the epitope is selected from I-helical surface regions of a cellular prion protein.
6. The method of claim 1 , wherein the epitope is selected from exposed surface regions of an infectious prion protein.
7. The method of claim 5 , wherein the sequence formed by the positions (b i c i e i f i g i ) n corresponds to the solvent-accessible residues of an epitope having a sequence selected from the group consisting of SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 7.
8. The method of claim 5 wherein the cellular prion protein is selected from the group consisting of mouse, hamster, bovine, ovine and human cellular prion proteins.