Saccharomyces cerevisiae can release hepatitis B virus surface antigen (HBsAg) particles into the medium by its secretory apparatus |
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Authors: | Shun'ichi Kuroda Takeshi Miyazaki Sachiko Otaka Yukio Fujisawa |
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Affiliation: | (1) Biotechnology Research Laboratories, Takeda Chemical Industries, Ltd., Yodogawa, 532 Osaka, Japan;(2) Present address: Discovery Research Laboratories II Department V, Discovery Research Division, Pharmaceutical Group, Takeda Chemical Industries, Ltd., 17-85 Juso-honmachi 2-chrome, Yodogawa, 532 Osaka, Japan |
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Abstract: | We constructed a plasmid that directs the synthesis and secretion of hepatitis B virus (HBV) surface antigen (HBsAg) particles by Saccharomyces cerevisiae. This plasmid contains a proteinase-resistant HBsAg M (M-P31c) gene fused at its 5'-terminus with a chicken-lysozyme signal peptide (C-SIG) gene, which is placed under the yeast GLD (glyceraldehyde-3-phosphate dehydrogenese gene) promoter. The products encoded by the C-SIG + M-P31c (LM-P31c) gene were synthesized and assembled themselves into HBsAg particles in yeast cells, and the particles were released into the medium along with poly-HSA (polymerized human serum albumin) binding activity. The HBsAg particles purified from the medium were very similar in density (1.19 g cm–3), size (19.2±0.8 nm in diameter) and shape (sphere) to human-plasma-derived HBsAg particles. When several sec (temperature-sensitive secretion-defective) mutants were used as host cells, the release of HBsAg particles into the medium was blocked at 37°C but not at 25°C, indicating that the HBsAg particles are exported through the normal yeast secretion pathway. To our knowledge, this is the first report that yeast cells are capable of secreting particles into the medium.Correspondence to: S. Kuroda |
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