Peptides and methods for the detection of lyme disease antibodies
The invention provides compositions (e.g., peptide compositions) useful for the detection of antibodies that bind to Borrelia antigens. The peptide compositions comprise polypeptide sequences comprising variants in the IR6 domain of the Borrelia VlsE protein. The invention also provides devices, methods, and kits comprising such peptide compositions and useful for the detection of antibodies that bind to Borrelia antigens and the diagnosis of Lyme disease.
1. A mixture of isolated peptides comprising three or more different isolated peptides, wherein at least one of said isolated peptides comprises the sequence of SEQ ID NO: 24, SEQ ID NO: 51, SEQ ID NO: 66, SEQ ID NO: 74, SEQ ID NO: 83, SEQ ID NO: 98, SEQ ID NO: 114, SEQ ID NO: 115, SEQ ID NO: 125, or SEQ ID NO: 144.
2. The mixture of claim 1 , wherein each isolated peptide is conjugated to a ligand.
3. The mixture of claim 1 , wherein one or more of the isolated peptides is biotinylated.
4. The mixture of claim 1 , wherein one or more of the isolated peptides is conjugated to streptavidin or bovine serum albumin optionally via an additional terminal amino acid linking residue.
5. The mixture of claim 4 , wherein the terminal amino acid linking residue is cysteine or lysine.
6. The mixture of claim 1 , wherein each isolated peptide is immobilized to a solid support.
7. The mixture of claim 1 , wherein each isolated peptide is attached to or immobilized on a bead, a flow path in a lateral flow immunoassay device, a well in a microtiter plate, or a flow path in a rotor.
8. The mixture of claim 1 , wherein one or more of the isolated peptides is conjugated to a colloidal nanoparticle.
9. The mixture of claim 8 , wherein the colloidal nanoparticle is a colloidal gold nanoparticle.
10. The mixture of claim 1 , wherein each isolated peptide comprises an additional N-terminal peptide sequence that is a native V1sE sequence or non-V1sE Borrelia antigen.
11. The mixture of claim 10 , wherein the additional N-terminal peptide sequence is a sequence of n 1 -n 2 -S-P-n 5 -n 6 -P (SEQ ID NO: 149) or a fragment thereof, wherein n 1 is an amino acid selected from the group consisting of A and V, n 2 is an amino acid selected from the group consisting of E and D, n 5 is an amino acid selected from the group consisting of K and R, and n 6 is an amino acid selected from the group consisting of K and R.
12. The mixture of claim 1 , wherein each isolated peptide comprises an additional C-terminal peptide sequence that is a native V1sE sequence or non-V1sE Borrelia antigen.
13. The mixture of claim 12 , wherein the additional C-terminal peptide sequence is a sequence of V-c 2 -E-G-c 5 -Q-Q-E-G-A-Q-Q-P-S-C(SEQ ID NO: 150) or a fragment thereof, wherein c 2 is an amino acid selected from the group consisting of Q and R, and c 5 is an amino acid selected from the group consisting of V and A.
14. The mixture of claim 12 , wherein the additional C-terminal peptide sequence is a sequence of A-V-c 3 -E-G-c 6 -Q-Q-E-G-A-Q-Q-P-S(SEQ ID NO: 151) or a fragment thereof, wherein c 3 is an amino acid selected from the group consisting of Q and R, and c 6 is an amino acid selected from the group consisting of V and A.
15. A kit comprising the mixture of isolated peptides of claim 1 and a labeling reagent capable of binding to an antibody that recognizes an epitope of at least one of the isolated peptides in the mixture.
16. The kit of claim 15 , wherein each isolated peptide in the mixture is attached to a solid support.
17. The kit of claim 15 , wherein each isolated peptide in the mixture is attached to a bead, a tube, a well, a lateral flow assay device, or an analytical rotor.
18. The kit of claim 15 , wherein the labeling reagent is
(i) an anti-human or anti-canine IgG antibody conjugated to a detectable label or
(ii) protein A and/or protein G conjugated to a detectable label.
19. The kit of claim 18 , wherein the detectable label is colloidal gold nanoparticles.