Modified transferrin fusion proteins
    2.
    发明申请
    Modified transferrin fusion proteins 审中-公开
    改性转铁蛋白融合蛋白

    公开(公告)号:US20060205037A1

    公开(公告)日:2006-09-14

    申请号:US11367692

    申请日:2006-03-06

    摘要: Modified fusion proteins of a transferrini moiety, a GLP-1 moiety and a linker moiety, with increased productivity, bioactivity and serum half-life are disclosed. Preferred fusion proteins include those modified so that the transferrin moiety exhibits no or reduced glycosylation. The fusion proteins of the invention are useful for the treatment of Type 2 diabetes, Type 1 diabetes, obesity, congestive heart failure, and non-fatty liver disease.

    摘要翻译: 公开了具有增加的生产力,生物活性和血清半衰期的转录子部分,GLP-1部分和接头部分的修饰融合蛋白。 优选的融合蛋白包括修饰的融合蛋白,使得转铁蛋白部分不显示或降低糖基化。 本发明的融合蛋白可用于治疗2型糖尿病,1型糖尿病,肥胖症,充血性心力衰竭和非脂肪性肝病。

    Transferrin fusion proteins libraries
    6.
    发明申请
    Transferrin fusion proteins libraries 审中-公开
    转铁蛋白融合蛋白文库

    公开(公告)号:US20060105387A1

    公开(公告)日:2006-05-18

    申请号:US10515429

    申请日:2003-08-28

    IPC分类号: C40B40/10 C07K14/79

    CPC分类号: C07K14/79

    摘要: Modified fusion proteins of transferrin and therapeutic proteins or peptides with increased serum half-life or serum stability are disclosed. Preferred fusion proteins include those modified so that the transferrin moiety exhibits no or reduced glycosylation, binding to iron and/or binding to the transferrin receptor.

    摘要翻译: 公开了具有增加的血清半衰期或血清稳定性的转铁蛋白和治疗性蛋白质或肽的修饰融合蛋白。 优选的融合蛋白包括经修饰的融合蛋白,使得转铁蛋白部分不显示或降低糖基化,结合铁和/或结合转铁蛋白受体。

    Modified vasoactive intestinal peptides
    9.
    发明授权
    Modified vasoactive intestinal peptides 有权
    改良的血管活性肠肽

    公开(公告)号:US09029505B2

    公开(公告)日:2015-05-12

    申请号:US12857103

    申请日:2010-08-16

    摘要: The present invention provides modified Vasoactive Intestinal Peptides (VIPs), encoding polynucleotides and vectors, as well as pharmaceutical compositions comprising the same. The invention further provides methods of making and using the modified VIP agents. In accordance with the invention the VIP exhibits an extended circulatory half-life, receptor-binding or biological potency, and/or altered receptor binding profile with respect to unmodified VIP.

    摘要翻译: 本发明提供了修饰的血管活性肽肽(VIPs),编码多核苷酸和载体,以及包含其的药物组合物。 本发明还提供了制备和使用经修饰的VIP试剂的方法。 根据本发明,VIP相对于未修饰的VIP显示出延长的循环半衰期,受体结合或生物效力和/或改变的受体结合特征。

    MODIFIED VASOACTIVE INTESTINAL PEPTIDES
    10.
    发明申请
    MODIFIED VASOACTIVE INTESTINAL PEPTIDES 有权
    改良的VASOACTIVE INTESTINAL PEPTIDES

    公开(公告)号:US20110178017A1

    公开(公告)日:2011-07-21

    申请号:US12857103

    申请日:2010-08-16

    摘要: The present invention provides modified Vasoactive Intestinal Peptides (VIPs), encoding polynucleotides and vectors, as well as pharmaceutical compositions comprising the same. The invention further provides methods of making and using the modified VIP agents. In accordance with the invention the VIP exhibits an extended circulatory half-life, receptor-binding or biological potency, and/or altered receptor binding profile with respect to unmodified VIP.

    摘要翻译: 本发明提供了修饰的血管活性肽肽(VIPs),编码多核苷酸和载体,以及包含其的药物组合物。 本发明还提供了制备和使用经修饰的VIP试剂的方法。 根据本发明,VIP相对于未修饰的VIP显示出延长的循环半衰期,受体结合或生物效力和/或改变的受体结合特征。