Cryptocaryoniasis, caused by Cryptocaryon irritans, is a significant threat to marine fish cultures in tropical and subtropical waters. However, controlling this disease remains a challenge. Fish infected with C. irritans acquires immunity; however, C. irritans is difficult to culture in large quantities, obstructing vaccine development using parasite cells. In this study, we established a method for expressing an arbitrary protein on the surface of Tetrahymena thermophila, a culturable ciliate, to develop a mimetic C. irritans. Fusing the signal peptide (SP) and glycosylphosphatidylinositol (GPI) anchor sequences of the immobilization antigen, a surface protein of C. irritans, to the fluorescent protein, monomeric Azami-green 1 (mAG1) of the stony coral Galaxea fascicularis, allowed protein expression on the surface and cilia of transgenic Tetrahymena cells. This technique may help develop transgenic Tetrahymena displaying parasite antigens on their cell surface, potentially contributing to the development of vaccines using "mimetic parasites".
Target Protein Expression on Tetrahymena thermophila Cell Surface Using the Signal Peptide and GPI Anchor Sequences of the Immobilization Antigen of Cryptocaryon irritans.
利用刺激隐核虫固定抗原的信号肽和 GPI 锚定序列在嗜热四膜虫细胞表面表达靶蛋白
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作者:Watanabe Yuho, Asada Masahito, Inokuchi Mayu, Kotake Maho, Yoshinaga Tomoyoshi
| 期刊: | Molecular Biotechnology | 影响因子: | 2.500 |
| 时间: | 2024 | 起止号: | 2024 Aug;66(8):1907-1918 |
| doi: | 10.1007/s12033-023-00824-w | 研究方向: | 细胞生物学 |
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