Identification of conserved peptide blocks in homologous polypeptides

1. A method for identifying at least one peptide block in a plurality of homologous polypeptides as being conserved and as comprising one or more peptides suitable for use in an immunogenic composition and manufacturing any one or more of the peptides from the identified at least one peptide block, the method comprising:

(a) identifying at least one peptide block within a multiple sequence alignment (MSA) of a plurality of homologous polypeptides, each peptide being the same length as the other peptides within the same peptide block, wherein the peptides within each of the at least one peptide block are 8-11 amino acids in length and, wherein each of the at least one peptide block is a region of homology found within the MSA, and wherein each of the at least one peptide block includes a peptide from each of the polypeptides in the MSA and comprises at least two unique peptides;

(b) for each of the at least one peptide block, determining a minimum required number of unique peptides within the peptide block such that the cumulative fraction of polypeptides in the MSA comprising one or more of the unique peptides is at least 95%;

(c) identifying at least one peptide block as conserved and as comprising one or more peptides suitable for use in an immunogenic composition if the minimum required number of unique peptides determined in step (b) is between 2 and 7; and

(d) manufacturing any one or more of the peptides from the at least one peptide block identified as conserved and as comprising one or more peptides suitable for use in an immunogenic composition in step (c).

2. The method of claim 1 , wherein the plurality of polypeptides in the MSA comprises subsets of homologous polypeptides, each subset being derived from a different species; and wherein at least one peptide block is further identified in step (c) as conserved if the unique peptides used to determine the minimum required number in step (b) also represent a cumulative fraction of at least 99% of the homologous polypeptides in each subset of homologous polypeptides in the MSA.

3. The method of claim 2 , wherein the plurality of species comprises different serotypes of a virus.

4. The method of claim 3 , wherein the virus is dengue virus.

5. The method of claim 3 , wherein the serotypes are selected from one or more of dengue virus (DENV)-1, DENV-2, DENV-3, and DENV-4.

6. The method of claim 3 , wherein the serotypes comprise DENV-1, DENV-2, DENV-3 and DENV-4.

7. The method of claim 1 , wherein the cumulative fraction of homologous polypeptides in the MSA comprising one or more of the unique peptides is at least 97% or at least 99%.

8. The method of claim 1 , wherein the minimum required number of unique peptides determined in step (b) is between 2 and 6.

9. The method of claim 1 , wherein the polypeptides in the MSA are derived from a virus.

10. The method of claim 9 , wherein the virus is from a family selected from the group consisting of: Retroviridae, Picornaviridae, Caliciviridae, Togaviridae, Flaviridae, Coronaviridae, Rhabdoviridae, Filoviridae, Paramyxoviridae, Orthomyxoviridae, Bunyaviridae, Arena viridae, Reoviridae, Birnaviridae, Hepadnaviridae, Parvoviridae, Papovaviridae, Adenoviridae, Herperviridae, Poxyiridae, and Iridoviridae.

11. The method of claim 9 , wherein the virus is selected from the group consisting of dengue virus (DENV), yellow fever virus (YFV), Japanese encephalitis virus (JEV), West Nile virus (WNV), and Tick-borne encephalitis virus (TBEV).

12. The method of claim 9 , wherein the virus is selected from the group consisting of norovirus, influenza virus, and human immunodeficiency virus.

13. The method of claim 1 , wherein the minimum required number of unique peptides determined in step (b) is between 2 and 5.