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    • 5. 发明授权
    • Phage with nuclear localization signal
    • 噬菌体与核定位信号
    • US06759231B2
    • 2004-07-06
    • US09844813
    • 2001-04-27
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • C12N120
    • C12N15/1037C12N15/85C12N15/86C12N15/87C12N2795/10343
    • A &lgr; phage with a nuclear localization signal has been obtained by constructing a vector capable of expressing a fused protein between a gpD protein constituting the head of a &lgr; phage and a nuclear localization signal sequence, transforming Escherichia coli with this vector, and propagating a mutant &lgr; phage which cannot express the gpD protein in E. coli in this transformant. It has been confirmed that the resulting &lgr; phage is capable of packaging &lgr; phage DNAs of 80% and 100% genome sizes. After further confirming that the nuclear localization signal exposed on the outside of the head of this phage, this phage has been microinjected into cells to analyze its nuclear localization activity. Thus, it has been clarified that this phage has a nuclear localization activity.
    • 已经通过构建能够在构成λ噬菌体的头部的gpD蛋白质和核定​​位信号序列之间表达融合蛋白质的载体,用该载体转化大肠杆菌并扩增突变体来获得具有核定位信号的λ噬菌体 λ噬菌体在该转化体中不能在大肠杆菌中表达gpD蛋白。 已经证实所得的λ噬菌体能够包装80%和100%基因组大小的λ噬菌体DNA。 在进一步证实核定位信号暴露在该噬菌体头部的外部时,该噬菌体已被微量注入细胞以分析其核定位活性。 因此,已经澄清这种噬菌体具有核定位活动。
    • 6. 发明授权
    • Phage bonded to a nuclear location signal
    • 噬菌体与核定位信号
    • US06235521B1
    • 2001-05-22
    • US09242131
    • 1999-09-10
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • Mahito NakanishiEmi NagoshiTeruo AkutaKatsuo TakedaMamoru Hasegawa
    • C12N700
    • C12N15/1037C12N15/85C12N15/86C12N15/87C12N2795/10343
    • A &lgr; phage with a nuclear localization signal has been obtained by constructing a vector capable of expressing a fused protein between a gpD protein constituting the head of a &lgr; phage and a nuclear localization signal sequence, transforming Escherichia coli with this vector, and propagating a mutant &lgr; phage which cannot express the gpD protein in E. coli in this transformant. It has been confirmed that the resulting &lgr; phage is capable of packaging &lgr; phage DNAs of 80% and 100% genome sizes. After further confirming that the nuclear localization signal exposed on the outside of the head of this phage, this phage has been microinjected into cells to analyze its nuclear localization activity. Thus, it has been clarified that this phage has a nuclear localization activity.
    • 通过构建能够在构成羔羊噬菌体的头部的gpD蛋白质和核定​​位信号序列之间表达融合蛋白的载体,通过该载体转化大肠杆菌并扩增突变体,获得具有核定位信号的羔羊噬菌体 在该转化体中不能在大肠杆菌中表达gpD蛋白的羔羊噬菌体。 已经证实,所得的羔羊噬菌体能够包装80%和100%基因组大小的羔羊噬菌体DNA。 在进一步证实核定位信号暴露在该噬菌体头部的外部时,该噬菌体已被微量注入细胞以分析其核定位活性。 因此,已经澄清这种噬菌体具有核定位活动。