Alteration of Fc-fusion protein serum half-lives by mutagenesis
    41.
    发明授权
    Alteration of Fc-fusion protein serum half-lives by mutagenesis 有权
    通过诱变改变Fc融合蛋白血清半衰期

    公开(公告)号:US07732570B2

    公开(公告)日:2010-06-08

    申请号:US11803694

    申请日:2007-05-14

    摘要: The present invention provides for a modified Fc-fusion protein in which at least one amino acid from the heavy chain constant region selected from the group consisting of amino acid residues 250, 314, and 428 is substituted with another amino acid which is different from that present in the unmodified Fc-fusion protein, thereby altering the binding affinity for FcRn and/or the serum half-life in comparison to the unmodified Fc-fusion protein.

    摘要翻译: 本发明提供了修饰的Fc融合蛋白,其中来自选自氨基酸残基250,314和428的重链恒定区的至少一个氨基酸被另一种不同于此的氨基酸取代 存在于未修饰的Fc融合蛋白中,从而与未修饰的Fc融合蛋白相比,改变了FcRn的结合亲和力和/或血清半衰期。

    Anti-CCR5 antibody
    43.
    发明授权
    Anti-CCR5 antibody 有权
    抗CCR5抗体

    公开(公告)号:US07666419B2

    公开(公告)日:2010-02-23

    申请号:US11581945

    申请日:2006-10-16

    摘要: The invention is directed an anti-CCR5 antibody which comprises (i) two light chains, each light chain comprising the expression product of a plasmid designated pVK:HuPRO14O-VK (ATCC Deposit Designation PTA-4097), and (ii) two heavy chains, each heavy chain comprising an expression product of either a plasmid designated pVgl:HuPRO140 HG2-VH (ATCC Deposit Designation PTA-4098) or a plasmic designated pVgl:HuPRO140 (mutB+D+I)-VH (ATCC Deposit Designation PTA-4099) or a fragment thereof which binds to CCR5 on the surface of a human cell.

    摘要翻译: 本发明涉及抗CCR5抗体,其包含(i)两条轻链,每条轻链包含命名为pVK:HuPRO14O-VK(ATCC保藏号PTA-4097)的质粒的表达产物,和(ii)两条重链 每个重链包含称为pVgl:HuPRO140HG2-VH(ATCC保藏号PTA-4098)或质粒命名为pVgl:HuPRO140(mutB + D + I)-VH(ATCC保藏号PTA-4099)的质粒的表达产物 )或其与人细胞表面上的CCR5结合的片段。

    Expression vectors
    44.
    发明授权
    Expression vectors 有权
    表达载体

    公开(公告)号:US08969539B2

    公开(公告)日:2015-03-03

    申请号:US12456007

    申请日:2009-06-10

    摘要: This present invention provides an expression vector system that uses alternative RNA processing to express in a single cell a polypeptide in both membrane-bound and soluble forms. By incorporating a mimetic structure of the 3′ terminal region of human mu gene and introducing other exogenous genetic elements, an artificial gene can be constructed that is capable of simultaneously expressing membrane-bound and secreted forms of polypeptides in myeloma cells and other cells of the B lymphocyte lineage, as well as in non-B cells. If an immunoglobulin heavy chain is co-expressed with a light chain using this vector, whole antibodies can be produced that are both displayed on the surface of a single cell and secreted into the cell culture supernatant. Membrane-bound antibodies facilitate isolation and expansion of those cells displaying antibodies with desired antigen binding characteristics, while secreted antibodies facilitate identification of antibodies having desired biological function(s).

    摘要翻译: 本发明提供了一种表达载体系统,其使用替代的RNA加工来在单细胞中以膜结合和可溶形式表达多肽。 通过掺入人mu基因的3'末端区域的模拟结构并引入其他外源遗传元件,可以构建人造基因,其能够同时表达骨髓瘤细胞和其它细胞中的多肽的膜结合和分泌形式 B淋巴细胞谱系,以及非B细胞。 如果使用该载体使免疫球蛋白重链与轻链共同表达,则可以产生全部抗体,其均显示在单个细胞的表面并分泌到细胞培养上清液中。 膜结合的抗体促进显示具有所需抗原结合特征的抗体的那些细胞的分离和扩增,而分泌的抗体便于鉴定具有所需生物学功能的抗体。

    Alteration of Fc-fusion protein serum half-lives by mutagenesis
    45.
    发明授权
    Alteration of Fc-fusion protein serum half-lives by mutagenesis 有权
    通过诱变改变Fc融合蛋白血清半衰期

    公开(公告)号:US08624007B2

    公开(公告)日:2014-01-07

    申请号:US12751914

    申请日:2010-03-31

    IPC分类号: C07H21/02 C07H21/04 C12P21/08

    摘要: The present invention provides for a modified Fc-fusion protein in which at least one amino acid from the heavy chain constant region selected from the group consisting of amino acid residues 250, 314, and 428 is substituted with another amino acid which is different from that present in the unmodified Fc-fusion protein, thereby altering the binding affinity for FcRn and/or the serum half-life in comparison to the unmodified Fc-fusion protein.

    摘要翻译: 本发明提供了修饰的Fc融合蛋白,其中来自选自氨基酸残基250,314和428的重链恒定区的至少一个氨基酸被另一种不同于此的氨基酸取代 存在于未修饰的Fc融合蛋白中,从而与未修饰的Fc融合蛋白相比,改变了FcRn的结合亲和力和/或血清半衰期。

    ALTERATION OF FC-FUSION PROTEIN SERUM HALF-LIVES BY MUTAGENESIS
    49.
    发明申请
    ALTERATION OF FC-FUSION PROTEIN SERUM HALF-LIVES BY MUTAGENESIS 有权
    FC融合蛋白血清半胱氨酸蛋白酶的变异

    公开(公告)号:US20110183412A1

    公开(公告)日:2011-07-28

    申请号:US12751914

    申请日:2010-03-31

    IPC分类号: C12N15/63 C07H21/00

    摘要: The present invention provides for a modified Fc-fusion protein in which at least one amino acid from the heavy chain constant region selected from the group consisting of amino acid residues 250, 314, and 428 is substituted with another amino acid which is different from that present in the unmodified Fc-fusion protein, thereby altering the binding affinity for FcRn and/or the serum half-life in comparison to the unmodified Fc-fusion protein.

    摘要翻译: 本发明提供了修饰的Fc融合蛋白,其中来自选自氨基酸残基250,314和428的重链恒定区的至少一个氨基酸被另一种不同于此的氨基酸取代 存在于未修饰的Fc融合蛋白中,从而与未修饰的Fc融合蛋白相比,改变了FcRn的结合亲和力和/或血清半衰期。

    Alteration of Fc-fusion protein serum half-lives by mutagenesis
    50.
    发明申请
    Alteration of Fc-fusion protein serum half-lives by mutagenesis 有权
    通过诱变改变Fc融合蛋白血清半衰期

    公开(公告)号:US20080287657A1

    公开(公告)日:2008-11-20

    申请号:US11803694

    申请日:2007-05-14

    IPC分类号: C07K16/18

    摘要: The present invention provides for a modified Fc-fusion protein in which at least one amino acid from the heavy chain constant region selected from the group consisting of amino acid residues 250, 314, and 428 is substituted with another amino acid which is different from that present in the unmodified Fc-fusion protein, thereby altering the binding affinity for FcRn and/or the serum half-life in comparison to the unmodified Fc-fusion protein.

    摘要翻译: 本发明提供了修饰的Fc融合蛋白,其中来自选自氨基酸残基250,314和428的重链恒定区的至少一个氨基酸被另一种不同于此的氨基酸取代 存在于未修饰的Fc融合蛋白中,从而与未修饰的Fc融合蛋白相比,改变了FcRn的结合亲和力和/或血清半衰期。