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    • 7. 发明申请
    • ALPHA INTERFERON VARIANTS
    • 阿尔法干扰素
    • WO2005035767A1
    • 2005-04-21
    • PCT/US2004/011965
    • 2004-04-16
    • BIOLEX, INC.DICKEY, LynnGASDASKA, JohnCOX, Kevin
    • DICKEY, LynnGASDASKA, JohnCOX, Kevin
    • C12N15/82
    • C12N15/8216C07K14/56C07K2317/55C12N15/8257
    • The present invention provides biologically active variants of human α-2b- interferon. The variants contain carboxy terminus truncations when compared with the amino acid sequence of full-length human α-2b-interferon. It is the novel finding of the present invention that these truncated variants have the biological activity of full-length human α-2b-interferon. The invention encompasses these biologically active variant α-interferons, as well as polynucleotides encoding these interferons. Expression cassettes comprising these polynucleotides and host cells comprising the expression cassettes are also provided. The invention also provides compositions comprising variant α-interferon polypeptides and a pharmaceutically acceptable carrier.
    • 本发明提供人α-2b-干扰素的生物活性变体。 当与全长人α-2b-干扰素的氨基酸序列相比时,变体含有羧基末端截短。 本发明的新发现是这些截短的变体具有全长人α-2b-干扰素的生物学活性。 本发明包括这些生物活性变体α-干扰素,以及编码这些干扰素的多核苷酸。 还提供了包含这些多核苷酸的表达盒和包含表达盒的宿主细胞。 本发明还提供包含变体α-干扰素多肽和药学上可接受的载体的组合物。
    • 10. 发明申请
    • COMPOSITIONS AND METHODS FOR PRODUCTION OF AGLYCOSYLATED PLASMINOGEN
    • 用于生产合成的PLASMINOGEN的组合物和方法
    • WO2010138631A1
    • 2010-12-02
    • PCT/US2010/036253
    • 2010-05-26
    • BIOLEX THERAPEUTICS, INC.DICKEY, Lynn, F.GASDASKA, John, R.COX, Kevin, M.
    • DICKEY, Lynn, F.GASDASKA, John, R.COX, Kevin, M.
    • C12N9/68A61K38/16C12N15/82C12N5/04C12N9/14
    • A61K38/168C12N9/6435C12N15/8257C12Y304/21007
    • Compositions and methods for producing aglycosylated plasminogen (PLG) polypeptides and fragments and variants thereof are provided. Compositions of the invention include isolated nucleic acid molecules encoding aglycosylated PLG polypeptides in which the asparagine (Asn) residue corresponding to residue Asn-289 of the mature human PLG polypeptide has been substituted with an amino acid residue that does not support N -linked glycosylation at that position of the PLG polypeptide, as well as the aglycosylated PLG polypeptides encoded thereby. Expression constructs comprising these PLG-encoding nucleic acid molecules and transgenic plants comprising these expression constructs are also provided. Methods of the invention comprise introducing a PLG-encoding nucleic acid molecule of the invention into a plant of interest and culturing the plant under conditions to produce the aglycosylated PLG polypeptide. The aglycosylated PLG polypeptide allows for significant increases in production and yield of PLG from a plant-based expression system without comprising the ability of the PLG product to be activated to a polypeptide capable of binding fibrin and having serine protease activity, including biologically active plasmin that is also aglycosylated. The activated aglycosylated plasmin is useful to treat diseases or conditions associated with a thrombus.
    • 提供了用于产生糖基化纤溶酶原(PLG)多肽及其片段和变体的组合物和方法。 本发明的组合物包括分离的编码糖基化PLG多肽的核酸分子,其中对应于成熟人PLG多肽的残基Asn-289的天冬酰胺(Asn)残基已被不支持N-连接糖基化的氨基酸残基取代 PLG多肽的位置,以及由此编码的糖基化的PLG多肽。 还提供了包含编码这些编码PLG的核酸分子和包含这些表达构建体的转基因植物的表达构建体。 本发明的方法包括将本发明的编码PLG的核酸分子引入感兴趣的植物中,并在产生糖苷基化的PLG多肽的条件下培养该植物。 糖基化的PLG多肽允许来自基于植物的表达系统的PLG的产量和产量的显着增加,而不包括PLG产物被活化到能够结合纤维蛋白并具有丝氨酸蛋白酶活性的多肽的能力,包括生物活性纤溶酶, 也糖基化。 活化的糖基化纤溶酶可用于治疗与血栓相关的疾病或病症。