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    • 7. 发明公开
    • METHODS FOR THE ISOLATION OF EXTRACELLULAR VESICLES AND OTHER BIOPARTICLES FROM URINE AND OTHER BIOFLUIDS
    • 方法细胞外微囊的和尿液和其它生物体液中的其他生物粒子
    • EP3177712A1
    • 2017-06-14
    • EP15830435.2
    • 2015-08-05
    • Ymir Genomics LLC
    • PENDERGRAST, P. ShannonPENDERGRAST, R. ScottPENDERGRAST, J. StephenMARKOWSKA, Anna Irmina
    • C12N5/07B01D9/02B01D21/26C07K1/30C07K14/705
    • B01D9/0054B01D21/26B01D21/262B01D2009/0086C07K1/30C07K1/303C07K1/306C07K14/705C12N15/1003G01N1/4055
    • Compositions and methods for the isolation of protein-nucleic acid complexes and microvesicles (collectively referred to as “bioparticles”) released by mammalian cells into body fluids or cell culture media are provided. Isolated bioparticles of the invention contain biological molecules that are useful as diagnostic/prognostic biomarkers or for identification of therapeutic targets (e.g., disease or disorder-associated miRNAs). The isolation of biological molecules as described herein results in purification and concentration of the molecules. Methods for producing bio fluids that are free of detectable bioparticles, that are largely depleted of bioparticles, or that possess a reduced concentration of bioparticles compared to a bio fluid starting material (collectively termed “bioparticle-depleted”) are also provided. Isolation of bioparticle-depleted biofluid is useful, e.g., in experimental systems where it is desirable to use a biofluid that does not contain endogenous bioparticles, or has been substantially depleted of endogenous bioparticles, from the source material.
    • 组合物和蛋白质 - 核酸复合物和微泡的分离方法(通过对统称为“生物颗粒”)由哺乳动物细胞释放到体液或细胞培养基中提供。 本发明的分离的生物颗粒包含生物分子确实可用作诊断/预后生物标记物或用于治疗靶标(例如,疾病或病症相关的miRNA)的识别是有用的。 生物分子的分离如在分子的纯化和浓缩的结果进行说明。 用于生产生物流体的方法那样被自由可检测生物颗粒的,并在很大程度上被耗尽生物颗粒,或确实拥有相较于生物流体原料(统称为“生物颗粒贫化”)被提供,因此生物颗粒的浓度降低。 生物颗粒耗尽生物流体的分离是有用的,e.g“在实验系统中,其中需要使用生物流体并不含有内源性生物颗粒,或已被基本耗尽的内源性生物颗粒的,从源材料。
    • 10. 发明公开
    • METHODS FOR STRUCTURAL DETERMINATION OF SELENIUM DERIVATIZED NUCLEIC ACID COMPLEXES
    • VERFAHREN ZUR STRUKTURBESTIMMUNG VON SELENDERIVATISITENTENNUKLEINSÄUREKOMPLEXEN
    • EP3071590A1
    • 2016-09-28
    • EP14863946.1
    • 2014-11-21
    • SeNA Research, Inc.
    • HUANG, Zhen
    • C07K1/14C07K1/30G01N33/53G01N33/68
    • A61K47/4823A61K38/465A61K47/61C07K1/30C12N9/22C12N9/96C12Y301/26004G01N33/5308G06F19/00G16H50/50Y02A90/26
    • Methods for crystallizing a molecule of interest, such as a polypeptide, in complex with nucleic acid, including contacting the molecule of interest with selenium-derivatized nucleic acid and crystallizing the molecule of interest/selenium-derivatized nucleic acid complex are provided. Methods for determining the X-ray crystal structure of molecule of interest/selenium-derivatized nucleic acid complexes are also provided. Typically, the method of X-ray crystal structural determination includes selenium single-wavelength anomalous phasing of the selenium-derivatized nucleic acid. In some embodiments the phases for the X-ray crystal structure of the molecule of interest are not provided from another crystal. Also disclosed are methods of affecting a biological process by administering a functional nucleic acid to a cell or a subject and/or by bringing into contact a nuclease and a functional nucleic acid, where the functional nucleic acid is selenium-derivatized nucleic acid.
    • 提供了与核酸复合的目标分子(例如多肽)结晶的方法,包括将感兴趣的分子与硒衍生的核酸接触并结晶感兴趣的分子/硒衍生的核酸复合物。 还提供了用于确定目的分子的X射线晶体结构/硒衍生的核酸复合物的方法。 通常,X射线晶体结构测定的方法包括硒衍生化核酸的硒单波长异常定相。 在一些实施方案中,感兴趣的分子的X射线晶体结构的相不是从另一晶体提供的。 还公开了通过向细胞或受试者施用功能性核酸和/或通过使功能性核酸为硒衍生化的核酸与核酸酶和功能性核酸接触来影响生物学过程的方法。