PEGYLATED ASPARTYL-TRNA SYNTHETASE POLYPEPTIDES
    1.
    发明申请
    PEGYLATED ASPARTYL-TRNA SYNTHETASE POLYPEPTIDES 有权
    聚乙二醇化的ASPARTYL-TRNA SYNTHETASE POLYPEPTIDES

    公开(公告)号:US20150159148A1

    公开(公告)日:2015-06-11

    申请号:US14360573

    申请日:2012-12-06

    Abstract: The present invention provides PEGylated aspartyl-tRNA synthetase (DRS) polypeptides, compositions comprising the same, and methods of using such polypeptides and compositions for treating or diagnosing a variety of conditions. The PEGylated DRS polypeptides of the invention have improved controlled release properties, stability, half-life, and other pharmacokinetic properties compared to non-PEGylated DRS polypeptides.

    Abstract translation: 本发明提供聚乙二醇化天冬氨酰-tRNA合成酶(DRS)多肽,包含其的组合物,以及使用这些多肽和组合物治疗或诊断各种病症的方法。 与非聚乙二醇化DRS多肽相比,本发明的聚乙二醇化DRS多肽具有改善的控制释放性质,稳定性,半衰期和其他药代动力学性质。

    ASPARTYL-TRNA SYNTHETASES
    2.
    发明申请

    公开(公告)号:US20140302075A1

    公开(公告)日:2014-10-09

    申请号:US14360576

    申请日:2012-12-06

    CPC classification number: C12N9/93 A61K38/00 C07K2319/40 Y02A50/411

    Abstract: The present invention provides aspartyl-tRNA synthetase derived proteins (DRS polypeptides) with altered cysteine content, compositions comprising the same, and methods of using such polypeptides and compositions for treating or diagnosing a variety of conditions. The DRS polypeptides of the invention have immunomodulatory properties, and exhibit improved activity and stability.

    Abstract translation: 本发明提供具有改变的半胱氨酸含量的天冬氨酰-tRNA合成酶衍生蛋白(DRS多肽),包含其的组合物,以及使用这些多肽和组合物治疗或诊断各种病症的方法。 本发明的DRS多肽具有免疫调节特性,并表现出改进的活性和稳定性。

    Histidyl-tRNA synthetase-Fc conjugates
    5.
    发明授权
    Histidyl-tRNA synthetase-Fc conjugates 有权
    组氨酰-tRNA合成酶-Fc偶联物

    公开(公告)号:US09587235B2

    公开(公告)日:2017-03-07

    申请号:US14214491

    申请日:2014-03-14

    CPC classification number: C12N9/93 C07K2319/30 C12N9/96 C12Y601/01021

    Abstract: The present invention provides histidyl-tRNA synthetase and Fc region conjugate polypeptides (HRS-Fc conjugates), such as HRS-Fc fusion polypeptides, compositions comprising the same, and methods of using such conjugates and compositions for treating or diagnosing a variety of conditions. The HRS-Fc conjugates of the invention have improved controlled release properties, stability, half-life, and other pharmacokinetic and biological properties relative to corresponding, unmodified HRS polypeptides.

    Abstract translation: 本发明提供组氨酰-tRNA合成酶和Fc区偶联物多肽(HRS-Fc缀合物),例如HRS-Fc融合多肽,包含其的组合物,以及使用这种缀合物和组合物治疗或诊断各种病症的方法。 本发明的HRS-Fc缀合物相对于相应的未修饰的HRS多肽具有改善的控制释放性质,稳定性,半衰期和其它药代动力学和生物学性质。

    HISTIDYL-TRNA SYNTHETASE-FC CONJUGATES

    公开(公告)号:US20140349369A1

    公开(公告)日:2014-11-27

    申请号:US14214491

    申请日:2014-03-14

    CPC classification number: C12N9/93 C07K2319/30 C12N9/96 C12Y601/01021

    Abstract: The present invention provides histidyl-tRNA synthetase and Fc region conjugate polypeptides (HRS-Fc conjugates), such as HRS-Fc fusion polypeptides, compositions comprising the same, and methods of using such conjugates and compositions for treating or diagnosing a variety of conditions. The HRS-Fc conjugates of the invention have improved controlled release properties, stability, half-life, and other pharmacokinetic and biological properties relative to corresponding, unmodified HRS polypeptides.

    Abstract translation: 本发明提供组氨酰-tRNA合成酶和Fc区偶联物多肽(HRS-Fc缀合物),例如HRS-Fc融合多肽,包含其的组合物,以及使用这种缀合物和组合物治疗或诊断各种病症的方法。 本发明的HRS-Fc缀合物相对于相应的未修饰的HRS多肽具有改善的控制释放性质,稳定性,半衰期和其它药代动力学和生物学性质。

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