Results

1. Construction of recombinant plasmid of HCV Core protein

1.1 Codon optimization of HCV core protein

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Fig.1 Part sequence of original (left) or optimized (right) HCV core protein at website http://gcua.schoedl.de/sequential_v2.html

optimized sequence of HCV core gene was showed as follows:

GGTACCATGAGTACCAATCCGAAACCGCAGCGCAAAACCAAACGTAATACCAATCGTCGTCCGGAAGATGTTAAATTTCCGGGCGGCGGTCAGATTGTGGGCGGCGTTTATCTGCTGCCGCGTCGTGGCCCGCGTC

TGGGTGTTCGTACCACCCGTAAAACCAGTGAACGCAGTCAGCCGCGCGGCCGCCGTCAACCTATTCCGAAAGATCGTCGCAGTACCGGCAAAGCCTGGGGCAAACCGGGCCGTCCGTGGCCTCTGTATGGTAATGAAGG

TCTGGGCTGGGCCGGTTGGCTGCTGAGCCCTCGTGGTAGTCGTCCGAGTTGGGGCCCGACCGATCCGCGTCATCGCAGTCGTAATGTGGGTAAAGTGATTGATACCCTGACCTGTGGCTTTGCAGATCTGATGGGCTAT

ATTCCGGTGGTTGGCGCACCGCTGAGCGGTGCAGCACGCGCAGTTGCACATGGCGTTCGTGTTCTGGAAGATGGTGTTAATTATGCCACCGGCAATCTGCCGGGCTTTCCGTTTAGTATTTTTCTGCTGGCCCTGCTGA

GCTGTATTACCGTGCCGGTGAGCGCCCTGCAG

1.2 PCR and confirmation of HCV C gene

For expression efficiently, the optimized and truncated HCV C genes, O173 (173AA) and O120 (120AA), were amplified using PCR method. The primers and PCR results are showed as below:

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Fig.2 Recycled enzyme-digested PCR products.

1.3 O173 and O120 genes were cloned into pColdII vector

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Fig.3 Before ligation of PCR products and pColdII, they were ldigested by restriction enzymes.

1.4 Identification of pColdII-O120 and pColdII-O173 recombinant plasmid

After ligation reactions, the products were transformed into the competent cell DH5α. We used colony PCR method to select the positive clones, and then send them to the company for sequencing. Colony PCR results were showed as below:

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Fig.4 Colony PCR products to identify the recombinant plasmids pColdII-O120 and pColdII-O173

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