DESIGNED ANKYRIN REPEAT DOMAINS WITH BINDING SPECIFICITY FOR SERUM ALBUMIN
    5.
    发明申请
    DESIGNED ANKYRIN REPEAT DOMAINS WITH BINDING SPECIFICITY FOR SERUM ALBUMIN 审中-公开
    设计用于血清白蛋白的具有结合特异性的ANKYRIN重复域

    公开(公告)号:WO2016156596A1

    公开(公告)日:2016-10-06

    申请号:PCT/EP2016/057272

    申请日:2016-04-01

    Abstract: New designed ankyrin repeat domains with binding specificity for serum albumin, recombinant binding proteins comprising at least two designed ankyrin repeat domains with binding specificity for serum albumin, as well as recombinant binding proteins comprising at least one designed ankyrin repeat domain with binding specificity for hepatocyte growth factor (HGF), at least one designed ankyrin repeat domain with binding specificity for vascular endothelial growth factor (VEGF-A), and at least two designed ankyrin repeat domain with binding specificity for serum albumin are described, as well as nucleic acids encoding such designed ankyrin repeat domains and recombinant binding proteins, pharmaceutical compositions comprising such designed ankyrin repeat domains, recombinant binding proteins or nucleic acids and the use of such designed ankyrin repeat domains, recombinant binding proteins, nucleic acids or pharmaceutical compositions in the treatment of diseases.

    Abstract translation: 新设计的对血清白蛋白具有结合特异性的锚蛋白重复结构域,包含至少两个设计的针对血清白蛋白结合特异性的设计的锚蛋白重复结构域的重组结合蛋白,以及包含至少一个设计的具有对肝细胞生长具有结合特异性的设计的锚蛋白重复结构域的重组结合蛋白 描述了至少一个具有对血管内皮生长因子(VEGF-A)具有结合特异性的至少一个设计的锚蛋白重复结构域和至少两个对血清白蛋白具有结合特异性的设计的锚蛋白重复结构域,以及编码这样的核酸 设计的锚蛋白重复结构域和重组结合蛋白,包含这种设计的锚蛋白重复结构域的药物组合物,重组结合蛋白或核酸,以及这些设计的锚蛋白重复结构域,重组结合蛋白,核酸或药物组合物在治疗疾病中的用途。

    PEPTIDE FOR TREATING INFLAMMATORY DISEASES
    6.
    发明申请
    PEPTIDE FOR TREATING INFLAMMATORY DISEASES 审中-公开
    用于治疗炎症疾病的肽

    公开(公告)号:WO2016116948A1

    公开(公告)日:2016-07-28

    申请号:PCT/IN2016/000025

    申请日:2016-01-21

    Applicant: RAM, Isanaka

    Inventor: RAM, Isanaka

    CPC classification number: C07K14/4703 A61K38/00 A61K38/20 C07K14/54

    Abstract: The present invention provides a peptide having anti-inflammatory activity. The present invention also provides the method of preparation of the peptide and compositions, and kits comprising the peptide. The invention further provides the method of treating inflammatory diseases employing the peptide of the present invention.

    Abstract translation: 本发明提供具有抗炎活性的肽。 本发明还提供了肽和组合物的制备方法以及包含该肽的试剂盒。 本发明还提供了使用本发明的肽治疗炎性疾病的方法。

    FORMULATION OF MK2 INHIBITOR PEPTIDES
    7.
    发明申请
    FORMULATION OF MK2 INHIBITOR PEPTIDES 审中-公开
    MK2抑制剂制剂的制备

    公开(公告)号:WO2016112292A1

    公开(公告)日:2016-07-14

    申请号:PCT/US2016/012650

    申请日:2016-01-08

    Abstract: The described invention provides pharmaceutical formulations comprising a polypeptide of amino acid sequence YARAAARQARAKALARQLGVAA (SEQ ID NO: 1 ) or a functional equivalent thereof with improved stability and bioavailability. According to one embodiment, the pharmaceutical formulation is a particulate pharmaceutical formulation. According to another aspect, the described invention provides a method for treating a vascular graft-induced intimal hyperplasia in a subject in need of such treatment.

    Abstract translation: 所述发明提供包含具有改善的稳定性和生物利用度的氨基酸序列YARAAARQARAKALARQLGVAA(SEQ ID NO:1)或其功能等同物的多肽的药物制剂。 根据一个实施方案,药物制剂是颗粒药物制剂。 根据另一方面,本发明提供了治疗需要这种治疗的受试者的血管移植物诱导的内膜增生的方法。

    PERMANENT EPIGENETIC GENE SILENCING
    9.
    发明申请
    PERMANENT EPIGENETIC GENE SILENCING 审中-公开
    永久性基因沉默

    公开(公告)号:WO2016063264A1

    公开(公告)日:2016-04-28

    申请号:PCT/IB2015/058202

    申请日:2015-10-23

    Abstract: A product comprising two or more artificial transcription repressors (ATRs), or polynucleotides encoding therefor, selected from groups (a), (b), (c) or (d): (a) an ATR comprising a DNA-binding domain operably linked to a KRAB domain or homologue thereof; (b) an ATR comprising a DNA-binding domain operably linked to a DNMT3A, DNMT3B or DNMT1 domain or homologue thereof; (c) an ATR comprising a DNA-binding domain operably linked to a DNMT3L domain or homologue thereof; and (d) an ATR comprising a DNA-binding domain operably linked to a SETDB1 domain or homologue thereof, wherein at least two of the ATRs are selected from different groups (a), (b), (c) or (d).

    Abstract translation: 选自(a),(b),(c)或(d)组的两种或更多种人工转录阻抑物(ATR)或其编码的多核苷酸的产物:(a)包含可操作地连接的DNA结合结构域的ATR 到KRAB结构域或其同源物; (b)ATR,其包含与DNMT3A,DNMT3B或DNMT1结构域或其同源物可操作地连接的DNA结合结构域; (c)包含可操作地连接到DNMT3L结构域或其同源物的DNA结合结构域的ATR; 和(d)ATR,其包含可操作地连接到SETDB1结构域或其同源物的DNA结合结构域,其中至少两个ATR选自不同的组(a),(b),(c)或(d)。

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