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    • 13. 发明申请
    • PERHYDROLASE EPITOPES
    • WO2007067473A3
    • 2007-09-07
    • PCT/US2006046203
    • 2006-12-04
    • GENENCOR INTHARDING FIONA A
    • HARDING FIONA A
    • C12N9/16C11D3/386G01N33/50
    • C12N9/18C11D3/38636C12N9/16G01N33/505
    • The present invention provides perhydrolase enzyme CD4+ T-cell epitopes, as well as variants that exhibit reduced immunogenic responses, as compared to the parental perhydrolase . The present invention further provides DNA molecules that encode perhydrolase variants, and host cells comprising DNA encoding perhydrolase variants, as well as methods for making perhydrolase enzymes less immunogenic. In addition, the present invention provides variou compositions that comprise perhydrolase variants that are less immunogenic than the wild- type perhydrolase. In some specific embodiments, the present invention provides perhydrolase variants with reduced immunogenicity identified and/or characterized using the methods of the present invention. These enzymes find use in cleaning and other applications. In some preferred embodiments, the present invention finds particular use in applications involving cleaning, bleaching and disinfecting.
    • 与亲本过氧化氢酶相比,本发明提供了过水解酶酶CD4 + T细胞表位,以及表现出降低的免疫原性应答的变体。 本发明还提供了编码过水解酶变体的DNA分子和包含编码过水解酶变体的DNA的宿主细胞,以及制备过水解酶较少免疫原性的方法。 此外,本发明提供了包含与野生型过水解酶相比较少免疫原性的过水解酶变体的变种组合物。 在一些具体实施方案中,本发明提供使用本发明的方法鉴定和/或表征的具有降低的免疫原性的过水解酶变体。 这些酶可用于清洁和其他应用。 在一些优选实施方案中,本发明特别用于涉及清洁,漂白和消毒的应用。
    • 20. 发明申请
    • HPV CD8+ T-CELL EPITOPES
    • HPV CD8 + T细胞EPITOPES
    • WO2005025497A3
    • 2005-06-02
    • PCT/US2004027263
    • 2004-08-23
    • GENENCOR INTHARDING FIONA AMUCHA JEANETTE MARIE
    • HARDING FIONA AMUCHA JEANETTE MARIE
    • A61K20060101A61K38/00C07H21/04C07K20060101C07K14/01C07K14/74C12N7/00C12P21/04C12Q1/68G01N33/50G01N33/53G01N33/567G01N33/68
    • G01N33/6878A61K2039/525C07K14/005C12N7/00C12N2710/20022G01N33/505G01N2333/70517G01N2333/70578
    • The present invention provides means to identify functional CD8+ T-cell epitopes in any protein of interest. The present invention further provides CD8+ T-cell epitopes of various proteins. In additional embodiments, the present invention provides epitopes suitable for use in prophylactic and/or therapeutic vaccines. In particularly preferred embodiments, the present invention provides modified epitopes suitable for use in prophylactic and/or therapeutic vaccines. In some preferred embodiments, the present invention provides means for the development of HPV vaccines, in particular multivalent vaccines for the prevention of infection with high-risk HPV strains. In particular, the present invention provides means to identify CD8+ T-cell epitopes in HPV strains such as HPV 16 and HPV 18. In additional embodiments, the present invention provides means for the development of therapeutic vaccines against high-risk HPV types that prevent the development of benign and/or malignant tumors in infected individuals. The present invention further provides epitopes suitable for use in prophylactic and therapeutic vaccines.
    • 本发明提供了鉴定任何感兴趣蛋白质中的功能性CD8 + T细胞表位的手段。 本发明进一步提供了各种蛋白质的CD8 + T细胞表位。 在另外的实施方案中,本发明提供了适用于预防性和/或治疗性疫苗的表位。 在特别优选的实施方案中,本发明提供了适用于预防性和/或治疗性疫苗的修饰表位。 在一些优选的实施方案中,本发明提供了开发HPV疫苗的手段,特别是用于预防高风险HPV毒株感染的多价疫苗。 具体而言,本发明提供了鉴定HPV菌株如HPV16和HPV18中的CD8 + T细胞表位的手段。在另外的实施方案中,本发明提供了开发针对高风险HPV类型的治疗性疫苗的手段, 在感染的个体中发展良性和/或恶性肿瘤。 本发明还提供了适用于预防性和治疗性疫苗的表位。