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    • 7. 发明公开
    • PROCESS FOR PRODUCING PROTEIN CAPABLE OF FORMING INCLUSION BODY
    • VERFAHREN ZUR HERSTELLUNG EINESEINSCHLUSSKÖRPER-BILDENDEN蛋白
    • EP2363469A1
    • 2011-09-07
    • EP09822044.5
    • 2009-10-21
    • The Chemo-Sero-Therapeutic Research InstituteTeijin Pharma Limited
    • NAKATAKE, HiroshiMETA, AkihiroSUENAGA, KiyotakaHIRASHIMA, MasakiMAEDA, Hiroaki
    • C12N15/09C12N1/21C12P21/02C12N9/64
    • C12N9/6491C07K2319/02C12P21/02
    • A process for preparing an inclusion body-forming protein is provided. A nucleic acid fragment consisting of a nucleotide sequence coding for a modified alkaline phosphatase signal peptide (modified APSP) where leucine at the 13th position in the amino acid sequence shown in SEQ ID NO: 1 is substituted with proline and/or alanine at the 21st position is substituted with the other amino acid, downstream of which nucleotide sequence is bound a nucleotide sequence of a gene of a protein of interest, and a process for preparing an inclusion body-forming protein consisting of the following steps: (1) preparing an expression vector in which a nucleic acid fragment is incorporated consisting of a nucleotide sequence coding for a modified signal peptide downstream of which is bound a nucleotide sequence of a gene of a protein of interest, (2) preparing a host cell transformed with the expression vector that produces an inclusion body-forming protein, and (3) purifying the inclusion body-forming protein from culture obtained by culturing the host cell that produces the inclusion body-forming protein. The above other amino acid is selected from the group consisting of aspartic acid, glutamic acid, lysine, histidine, phenylalanine and tyrosine.
    • 提供了制备包涵体形成蛋白的方法。 由编码改变的碱性磷酸酶信号肽(修饰的APSP)的核苷酸序列组成的核酸片段,其中第21位的氨基酸序列中的第13位的亮氨酸被脯氨酸和/或丙氨酸取代 位置被其他氨基酸取代,其中核苷酸序列的下游与感兴趣蛋白质的基因的核苷酸序列结合,以及由以下步骤组成的包含体形成蛋白的方法:(1)制备 表达载体,其中掺入核酸片段,由编码下游的修饰信号肽的核苷酸序列组成,所述核苷酸序列结合目的蛋白质的基因的核苷酸序列,(2)制备用表达载体转化的宿主细胞 产生包涵体形成蛋白质,(3)通过培养产生的宿主细胞获得的培养物纯化包涵体形成蛋白质 是包涵体形成蛋白。 上述其它氨基酸选自天冬氨酸,谷氨酸,赖氨酸,组氨酸,苯丙氨酸和酪氨酸。
    • 8. 发明公开
    • PEPTIDE FRAGMENTS HAVING CELL DEATH INHIBITORY ACTIVITY
    • PEPTIDFRAGMENTE MIT DEN ZELLTOD VERHINDERNDERAKTIVITÄT
    • EP1132402A1
    • 2001-09-12
    • EP99972642.5
    • 1999-11-12
    • Juridical Foundation, The Chemo-Sero-Therapeutic Research Institute
    • HIRASHIMA, MasakiMAEDA, HiroakiNOZAKI, Chikateru
    • C07K14/47A61K38/17C12N5/06C07K16/18
    • C07K14/4747A61K38/00
    • The present invention provides a peptide fragment or a series of peptide fragments having a cell death-inhibitory activity, having the amino acid sequence consisting of 103 amino acid residues at the C-terminal of selenoprotein P, or having said amino acid sequence with one or several amino acid residues therein being deleted, substituted or added, or having a partial sequence of either of the above amino acid sequences, a medicament for treatment comprising said peptide fragment or a series of peptide fragments, an antibody to said peptide fragment or a series of peptide fragments, and a method for screening a cell death-inhibitory activity using said peptide fragment or a series of peptide fragments. The preferable peptide fragment or a series of peptide fragments of the present invention has the amino acid sequences shown in SEQ ID NO: 1 and/or SEQ ID NO: 2 or has a partial sequence thereof.
    • 本发明提供具有细胞死亡抑制活性的肽片段或一系列肽片段,其具有由硒蛋白P的C末端上的103个氨基酸残基组成的氨基酸序列,或具有所述氨基酸序列与一个或多个 其中缺少,取代或添加的几个氨基酸残基或具有上述氨基酸序列之一的部分序列,包含所述肽片段或一系列肽片段的治疗药物,所述肽片段的抗体或一系列 的肽片段,以及使用所述肽片段或一系列肽片段筛选细胞死亡抑制活性的方法。 本发明优选的肽片段或一系列肽片段具有SEQ ID NO:1和/或SEQ ID NO:2所示的氨基酸序列或其部分序列。