Mycobacteria tuberculosis chaperonin 60.1 peptides and uses thereof
The present invention relates to novel peptides derivable from the polypeptide chaperonin 60.1 and to their use in medicine, such as for the prevention and/or treatment of inflammatory conditions.
1. An isolated or recombinant peptide molecule consisting of an amino acid sequence selected from one of the group (i) to (viii):
(i)
(SEQ ID NO: 2)
XHGLNVNTLSYGD
wherein X is absent or is selected from the group consisting of a beta alanine residue, 9-amino-3,6-dioxaoctanoic acid, and an acetyl group; or variants thereof comprising one or more of i(i) to i(iii);
i(i) one or more amino acid residues are in the D conformation,
i(ii) GLNVNTLSYGD (SEQ ID NO: 26) is inverted, or
i(iii) the carboxyl terminal amino acid residue is converted to a primary carboxamide group
(ii)
(SEQ ID NO: 3)
DGSVVVNKVSEL-NH2;
(iii)
(SEQ ID NO: 4)
SELPAGHGLNVNTLSYGDLAAD;
(iv)
(SEQ ID NO: 5)
SELPAGHGLNVNTLS;
(v)
(SEQ ID NO: 6)
PAGHGLNVNTLS-NH2;
(vi)
(SEQ ID NO: 7)
VVVNKVSELPAGHGLNVNTLSYGDLAAD;
(vii)
(SEQ ID NO: 8)
NKVSELPAGHGLNVNTLSYGDLAAD;
(viii)
(SEQ ID NO: 9)
PAGHGLNVNTLSYGDLAAD;
and
(ix)
(SEQ ID NO: 10)
HGLNVNTLSYGDLAAD.
2. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence selected from one of the group (a) to (m):
(a)
(SEQ ID NO: 11)
XHGLNVNTLSYGD-NH2
(b)
(SEQ ID NO: 12)
XdGysltnvnlGh-NH2;
(c)
(SEQ ID NO: 13)
XhGlnvntlsyGd-NH2;
(d)
(SEQ ID NO: 14)
hGLNVNTLSYGd-NH2;
(e)
(SEQ ID NO: 15)
HGLNVNTLSYGd-NH2;
(f)
(SEQ ID NO: 16)
hGLNVNTLSYGD-NH2;
(g)
(SEQ ID NO: 3)
DGSVVVNKVSEL-NH2;
(h)
(SEQ ID NO: 4)
SELPAGHGLNVNTLSYGDLAAD;
(i)
(SEQ ID NO: 5)
SELPAGHGLNVNTLS;
(j)
(SEQ ID NO: 6)
PAGHGLNVNTLS-NH2;
(k)
(SEQ ID NO: 7)
VVVNKVSELPAGHGLNVNTLSYGDLAAD;
(l)
(SEQ ID NO: 8)
NKVSELPAGHGLNVNTLSYGDLAAD;
(m)
(SEQ ID NO: 9)
PAGHGLNVNTLSYGDLAAD;
and
(n)
(SEQ ID NO: 10)
HGLNVNTLSYGDLAAD;
wherein upper case denotes an L-amino acid residue, lower case denotes a D-amino acid residue, X is absent or is selected from the group consisting of a beta alanine residue, 9-amino-3,6-dioxaoctanoic acid, and an acetyl group.
3. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence HGLNVNTLSYGD-NH2 (SEQ ID NO: 17).
4. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence bAla-HGLNVNTLSYGD-NH2 (SEQ ID NO: 18).
5. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence Ac-dGysltnvnlGh-NH2 (SEQ ID NO: 19), Ac-hGlnvntlsyGd-NH2 (SEQ ID NO: 20).
6. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence hGLNVNTLSYGd-NH2 (SEQ ID NO: 14) or a functionally equivalent fragment or variant thereof; or an amino acid sequence HGLNVNTLSYGd-NH2 (SEQ ID NO: 15).
7. The isolated or recombinant peptide molecule according to claim 1 , consisting of an amino acid sequence hGLNVNTLSYGD-NH2 (SEQ ID NO: 16) or a functionally equivalent fragment or variant thereof; or an amino acid sequence DGSVVVNKVSEL-NH2 (SEQ ID NO: 3).
8. A pharmaceutical composition comprising the peptide molecule according to claim 1 and one or more pharmaceutically-acceptable excipients.
9. The pharmaceutical composition according to claim 8 , further comprising one or more additional therapeutic agents.
10. The pharmaceutical composition according to claim 9 , wherein the additional therapeutic agent is selected from disease modifying agents, analgesics, broncodilators, anti-inflammatory agents, anti-allergic drugs, allergen immunotherapeutic agents, antivirals, antibiotics, antibodies and steroids.
11. The pharmaceutical composition according to claim 9 , wherein the additional therapeutic agent is selected from corticosteroids, anti-leukotrienes, cytokine monoclonal antibodies and theophylline.