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    • 3. 发明公开
    • NOVEL ADAMTS-13 MUTANT
    • 新的ADAMTS-13突变体
    • EP2172544A1
    • 2010-04-07
    • EP08777372.7
    • 2008-06-19
    • Juridical Foundation The Chemo-Sero-Therapeutic Research Institute
    • SOEJIMA, Kenji
    • C12N9/64A61K38/00A61P7/02A61P43/00C12N15/09
    • C12N9/6489A61K38/00A61K38/4886C12Y304/24087
    • The present invention provides a method of enhancing an enzymatic activity of ADAMTS-13 and/or a method of reducing reactivity to an anti-ADAMTS-13 neutralizing antibody as well as a mutant of ADAMTS-13 prepared by the methods. The method of the present invention is characterized by substituting at least one charged amino acid in a disintegrin-like domain, a cysteine-rich domain or a spacer domain of ADAMTS-13 other than the following amino acids with a different amino acid: arginine at position 326, aspartic acid at position 330, aspartic acid at position 343 and arginine at position 349 in the disintegrin-like domain, aspartic acid at position 480, arginine at position 488, arginine at position 498, arginine at position 507, aspartic acid at position 533 and aspartic acid at position 543 in the cysteine-rich domain, and glutamic acid at position 641 and arginine at position 660 in the spacer domain. The present invention also provides a therapeutic agent for thrombotic disease comprising as an active ingredient the mutant of ADAMTS-13 prepared by the method.
    • 本发明提供了增强ADAMTS-13的酶活性的方法和/或降低对抗ADAMTS-13中和抗体的反应性的方法以及通过所述方法制备的ADAMTS-13的突变体。 本发明的方法的特征在于用不同于下列氨基酸的ADAMTS-13的解聚素样结构域,富半胱氨酸结构域或间隔区中的至少一个带电氨基酸替换为不同的氨基酸:精氨酸 第326位,第330位天冬氨酸,第343位天冬氨酸和第349位精氨酸,第480位天冬氨酸,第488位精氨酸,第498位精氨酸,第507位精氨酸,第507位天冬氨酸 533位和天冬氨酸位于富含半胱氨酸结构域的543位,谷氨酸位于位置区641位,精氨酸位于660位。 本发明还提供了一种用于血栓性疾病的治疗剂,其包含通过该方法制备的ADAMTS-13突变体作为活性成分。
    • 4. 发明公开
    • PROCESS FOR PRODUCING HUMAN THROMBIN BY GENE MODIFICATION TECHNIQUE
    • VERFAHREN ZUR HERSTELLLUNG VON MENSCHLICHEM THROMBIN MITTELS GENMODIFIKATIONSTECHNIK
    • EP1405910A1
    • 2004-04-07
    • EP02743820.9
    • 2002-07-04
    • Juridical Foundation, The Chemo-Sero-Therapeutic Research Institute
    • YONEMURA, HiroshiIMAMURA, TakayukiNAKATAKE, HiroshiSOEJIMA, KenjiNOZAKI, Chikateru
    • C12N15/09C12P21/02
    • C12N9/6424C12Y304/21005
    • A genetic recombinant human thrombin is provided. Human thrombin is efficiently prepared by the genetic engineering technique comprising the steps: (1) culturing a transfectant animal cell transfected with an expression vector in which a gene encoding human prethrombin is incorporated to the downstream of a promoter so as to produce and accumulate prethrombin in culture supernatant and recovering the produced human prethrombin; (2) treating a solution containing human prethrombin recovered in step (1) with ecarin so as to convert human prethrombin into human thrombin; and (3) purifying the solution obtained after the above activation process to obtain purified human thrombin. The present invention allows for provision of human thrombin in a large scale in a safe and economical manner due to exclusion of blood-derived components.
    • 使用包含培养转化体的基因修饰技术生产人凝血酶,通过用艾卡林处理活化后将回收的人凝血酶原转化为人凝血酶,并从反应混合物中纯化人凝血酶是新的。 使用基因修饰技术生产人凝血酶包括:(a)培养通过将携带编码凝血酶原基因的基因的表达载体转化到动物细胞构建的转化体,所述基因整合到启动子的下游,并将如此产生的凝血酶原聚集在细胞中 收集培养基 (b)通过用艾卡林处理活化后将回收的人凝血酶原转化为人凝血酶; 和(c)从反应混合物中纯化此类人凝血酶。 活动:止血。 没有给出生物数据。 行动机制:无给予。