Synthetic hepatitis C polypeptide and methods of making and using same
Synthetic representative HCV subtypes, including a 1a and 1b genome, dubbed Bole1a and Bole1b, are provided using an inventive method of Bayesian phylogenetic tree analysis, ancestral sequence reconstruction and covariance analysis. Bole1a branches centrally among 390 full-genome sequences used in its design, a carefully curated 143 sequence full-genome dataset, and separate genomic regions including an independent set of 214 E1E2 sequences from a Baltimore cohort. Bole1a is phylogenetically representative of widely circulating strains. Full genome non-synonymous diversity comparison and 9-mer peptide coverage analysis showed that Bole1a is able to provide more coverage (94% and 78% respectively) than any other sequence in the dataset including H77, a traditional reference sequence. Bole1a also provides unsurpassed epitope coverage when compared to all known T cell epitopes.
1. The polypeptide encoded by a nucleic acid comprising SEQ ID NO: 1, encoding the genome of the synthetic hepatitis C virus subtype 1a (Bole 1a).
2. The polypeptide of claim 1 , comprising the amino acid sequence of SEQ ID NO: 2.
3. A viral particle comprising:
a) the last 27 amino acids encoded by of the core sequence of SEQ ID NO: 1 followed by the amino acid sequences of the E1 and E2 regions; and
b) a reporter element.
4. The viral particle of claim 3 , wherein the reporter element comprises the luciferase polyprotein or a functional portion thereof.