Intracellular glucocorticoid-induced leucine zippers modulators of apoptic cell death pathways
    1.
    发明授权
    Intracellular glucocorticoid-induced leucine zippers modulators of apoptic cell death pathways 失效
    细胞内糖皮质激素诱导的亮氨酸拉链调节剂的凋亡细胞死亡途径

    公开(公告)号:US06833348B1

    公开(公告)日:2004-12-21

    申请号:US09403861

    申请日:2000-02-11

    Applicant: Carlo Riccardi

    Inventor: Carlo Riccardi

    CPC classification number: C07K14/4703 A61K38/00 A61K48/00 C07K14/4705

    Abstract: A DNA sequence encoding a glucocorticoid-induced leucine-zipper family related protein (GILR), isoforms, fragments or analogs thereof said GILR, isoforms, fragments or analogs thereof capable of inhibiting apoptosis and stimulating lymphocyte activity, GILR proteins, isoforms, analogs, fragments and derivatives thereof encoded by the aforesaid DNA sequence, their preparation and uses.

    Abstract translation: 编码糖皮质激素诱导的亮氨酸 - 拉链家族相关蛋白(GILR),同种型,其片段或类似物的DNA序列说明能够抑制凋亡和刺激淋巴细胞活性的GILR,同工型,其片段或类似物,GILR蛋白,同种型,类似物,片段 及其衍生物,其制备和用途。

    Interferon-beta fusion proteins and uses
    2.
    发明授权
    Interferon-beta fusion proteins and uses 失效
    干扰素-β-1a免疫球蛋白融合蛋白及其用途

    公开(公告)号:US06800735B2

    公开(公告)日:2004-10-05

    申请号:US09832659

    申请日:2001-04-11

    CPC classification number: C07K14/565 A61K38/00 C07K2319/00 C07K2319/30

    Abstract: A fusion polypeptide is described having the amino acid sequence X-Y-Z, or portion thereof, comprising the amino acid sequence of a glycosylated interferon-beta (X); Y is an optional linker moiety; and Z is a polypeptide comprising at least a portion of a polypeptide other than glycosylated interferon-beta. It is preferred that X is human interferon-beta-1a. Mutants of interferon-beta-1a are also described.

    Abstract translation: 描述了融合多肽,其具有包含糖基化干扰素-β(X)的氨基酸序列的氨基酸序列X-Y-Z或其部分。 Y是任选的接头部分; Z是包含至少一部分除糖基化干扰素-β以外的多肽的多肽。 优选X是人干扰素-β-1a。 还描述了干扰素-β-1a的突变体。

    Modified G protein sunbunits
    6.
    发明授权
    Modified G protein sunbunits 失效
    改良的G蛋白日光浴

    公开(公告)号:US06448377B1

    公开(公告)日:2002-09-10

    申请号:US09672239

    申请日:2000-09-27

    CPC classification number: G01N33/68 G01N2333/726 G01N2500/00

    Abstract: The present invention provides modified G protein &agr;-subunits which are characterized by constitutive localization to the plasma membrane; enhanced binding to one or more of the normal receptor binding partners for that &agr;-subunit; and efficient binding to and activation of G protein binding partners. The distribution of these modified &agr;-subunits, which are “tethered” to the plasma membrane, allows the regulation of receptor-G protein coupling, and thus G-protein signaling, in various biological systems.

    Abstract translation: 本发明提供修饰的G蛋白α亚基,其特征在于质膜定位到质膜; 增强与该α-亚基的一个或多个正常受体结合配偶体的结合; 并有效结合和激活G蛋白结合配偶体。 这些经修饰的α亚基的“拴系”到质膜中的分布允许在各种生物系统中调节受体-G蛋白偶联,从而调节G蛋白信号传导。

    Compositions of highly-purified natural mixtures of type I Interferon derived from leukocytes and methods
    7.
    发明授权
    Compositions of highly-purified natural mixtures of type I Interferon derived from leukocytes and methods 失效
    来自白细胞的I型干扰素的高度纯化天然混合物的组合物和方法

    公开(公告)号:US06433144B1

    公开(公告)日:2002-08-13

    申请号:US09229039

    申请日:1999-01-12

    CPC classification number: C07K14/56 A61K38/00

    Abstract: This invention relates to methods for isolating highly purified mixtures of natural Type I interferon from white blood cells. The invention also relates to highly-purified mixtures of Type I interferon which resemble natural Type I interferon in that the highly purified mixtures of natural Type I interferon includes at least 9 subtypes, i.e., alpha-1, alpha-2, alpha-5, alpha-7, alpha-8, alpha-10, alpha-14, alpha-21 and omega, giving rise to at least 16, and possibly 20 or more molecular species, including alpha-1a, alpha-1new, alpha-2a, alpha-2b, alpha-2c, alpha-5, alpha-5LG, alpha-7, alpha-8a, alpha-8c, alpha-10a, alpha-14a, alphal4-b, alpha 14-c, alpha-14LG, alpha-21a, alpha-21b, alpha-21c, omega and omega LG.

    Abstract translation: 本发明涉及从白细胞中分离出高度纯化的天然I型干扰素混合物的方法。 本发明还涉及类似于天然I型干扰素的I型干扰素的高度纯化的混合物,因为天然I型干扰素的高度纯化的混合物包括至少9种亚型,即α-1,α-2,α-5, α-7,α-8,α-10,α-14,α-21和ω,产生至少16种,并且可能有20种或更多种分子物质,包括α-1a,α-1新,α-2a, α-2b,α-2c,α-5,α-5LG,α-7,α-8a,α-8c,α-10a,α-14a,alphal4-b,α14-c,α-14LG, -21a,α-21b,α-21c,ω和ωLG。

    Placenta derived apoptotic factor
    9.
    发明授权
    Placenta derived apoptotic factor 失效
    胎盘素衍生的凋亡因子

    公开(公告)号:US06689867B1

    公开(公告)日:2004-02-10

    申请号:US09684327

    申请日:2000-10-10

    CPC classification number: C07K14/47

    Abstract: The invention provides the nucleic acid and amino acid sequences of a novel human tumor-associated antigen, planenta derived apoptotic factor (PDAF), and the use of these sequences in the treatment of disorders associated with immune and cell proliferation.

    Abstract translation: 本发明提供新的人肿瘤相关抗原,平均衍生的凋亡因子(PDAF)的核酸和氨基酸序列,以及这些序列用于治疗与免疫和细胞增殖相关的病症的用途。

    Method for removing a chemokine
    10.
    发明授权
    Method for removing a chemokine 失效
    去除趋化因子的方法

    公开(公告)号:US06559290B1

    公开(公告)日:2003-05-06

    申请号:US08819630

    申请日:1997-03-17

    CPC classification number: B01D15/00 C07K14/521

    Abstract: An adsorbent for removing a chemokine except interleukin-8 in body fluid, which comprises a solid material having an anionic functional group, a method for efficiently removing a chemokine except interleukin-8 in body fluid, which comprises by bringing the above adsorbent into contact with body fluid containing the chemokine and an adsorber for removing a chemokine except for interleukin-8 using the above adsorbent.

    Abstract translation: 一种用于除去体液中除白介素-8之外的趋化因子的吸附剂,其包含具有阴离子官能团的固体材料,用于有效除去体液中白细胞介素-8的趋化因子的方法,其包括通过使上述吸附剂与 含有趋化因子的体液和除了使用上述吸附剂的白细胞介素-8以外的趋化因子的吸附器。

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