Pharmaceutical composition for treating liver diseases
    351.
    发明授权
    Pharmaceutical composition for treating liver diseases 有权
    用于治疗肝脏疾病的药物组合物

    公开(公告)号:US09469854B2

    公开(公告)日:2016-10-18

    申请号:US14873275

    申请日:2015-10-02

    Abstract: The present invention relates to a pharmaceutical composition for treating liver diseases, comprising a miRNA mimic containing a single strand RNA molecule of hsa-miR-21-3p (SEQ ID No: 35). The miRNA mimic of the present invention can be used to treat liver diseases through regulating the expression of methionine adenosyltransferase 2A and 2B (MAT2A and MAT2B), acetyl-CoA carboxylase 1 and 2 (ACACA and ACACB), diglyceride acyltransferase 2 (DGAT2), and so on. In addition, the present invention also relates to a method for reducing the expression of the above-mentioned enzymes.

    Abstract translation: 本发明涉及用于治疗肝脏疾病的药物组合物,其包含含有hsa-miR-21-3p(SEQ ID No:35)的单链RNA分子的miRNA模拟物。 本发明的miRNA模拟物可用于通过调节甲硫氨酸腺苷转移酶2A和2B(MAT2A和MAT2B),乙酰辅酶A羧化酶1和2(ACACA和ACACB),甘油二酯酰基转移酶2(DGAT2)的表达来治疗肝脏疾病。 等等。 此外,本发明还涉及降低上述酶表达的方法。

    Heat stable keratinase and use thereof
    352.
    发明授权
    Heat stable keratinase and use thereof 有权
    热稳定角蛋白酶及其用途

    公开(公告)号:US09434934B2

    公开(公告)日:2016-09-06

    申请号:US14903194

    申请日:2014-07-17

    Abstract: A fusion gene encoding M. taiwanensis WR-220 keratinase is disclosed. The fusion comprises: (a) a first DNA sequence encoding a protein secretion signal peptide, located at the N-terminus of the fusion gene; (b) a second DNA sequence encoding an inhibitory domain of M. taiwanensis WR-220 keratinase, linked in translation frame with the first DNA sequence; and (c) a third DNA sequence encoding a catalytic domain of M. taiwanensis WR-220 keratinase, linked in translation frame with the second DNA sequence, wherein the fusion gene is a non-naturally occurring chimeric DNA. Also disclosed are a method for preparation of the catalytic domain of M. taiwanensis WR-220 keratinase, and use of the M. taiwanensis WR-220 keratinase.

    Abstract translation: 公开了一种编码台湾华ensis WR-220角蛋白酶的融合基因。 融合物包含:(a)编码位于融合基因N末端的蛋白质分泌信号肽的第一DNA序列; (b)编码与第一DNA序列连接的翻译框架的台湾华ensis WR-220角蛋白酶的抑制结构域的第二DNA序列; 和(c)编码与第二DNA序列连接的翻译框架的台湾华南WR-220角蛋白酶的催化结构域的第三DNA序列,其中融合基因是非天然存在的嵌合DNA。 还公开了一种制备M. taiwanensis WR-220角蛋白酶的催化结构域的方法,并使用了台湾华氏WR-220角蛋白酶。

    Large scale enzymatic synthesis of oligosaccharides
    355.
    发明授权
    Large scale enzymatic synthesis of oligosaccharides 有权
    大规模酶促合成低聚糖

    公开(公告)号:US09340812B2

    公开(公告)日:2016-05-17

    申请号:US13971353

    申请日:2013-08-20

    CPC classification number: C12P19/18 C12P19/04 C12Y207/0701

    Abstract: A novel UDP-Gal regeneration process and its combined use with a galactosyltransferase to add galactose to a suitable acceptor substrate. Also described herein are synthetic methods for generating Globo-series oligosaccharides in large scale, wherein the methods may involve the combination of a glycosyltransferase reaction and a nucleotide sugar regeneration process.

    Abstract translation: 一种新型的UDP-Gal再生过程及其与半乳糖基转移酶的组合使用,以将半乳糖加入合适的受体底物。 本文还描述了大规模生产Globo系列寡糖的合成方法,其中所述方法可涉及糖基转移酶反应和核苷酸糖再生过程的组合。

    Robust and low backpressure on-column tunneled frit for nano-UPLC-MS applications
    357.
    发明授权
    Robust and low backpressure on-column tunneled frit for nano-UPLC-MS applications 有权
    用于纳米UPLC-MS应用的坚固和低背压柱上隧道玻璃料

    公开(公告)号:US09267927B2

    公开(公告)日:2016-02-23

    申请号:US13112519

    申请日:2011-05-20

    CPC classification number: G01N30/603 B01D15/22 G01N30/6078

    Abstract: A durable on-column tunneled frit was developed for use in nanoflow UPLC systems. The frit was tunneled during sol-gel reaction. The tunneled-frit fabrication process is easy and reproducible in terms of back pressure and durability. This design creates low backpressure with high liquid flow, which is suitable for the nanoflowUPLC application. A short packing (2 cm C18 particle) tunneled-frit column was demonstrated to sustain 10,000 psi continuous liquid flow for over one week without any particle leakage or pressure instability. The tunneled-frit was also successfully applied to the fabrication of nanoUPLC trapping and analytical column system. It was demonstrated to have high separation efficiency and sensitivity for the analysis of tryptic peptides as well as improved detection sensitivity for phosphopeptide analysis.

    Abstract translation: 开发了一种耐用的柱内隧道玻璃料,用于纳流低压UPLC系统。 玻璃料在溶胶 - 凝胶反应过程中被隧道化。 隧道式玻璃料制造工艺在背压和耐久性方面是容易的和可再现的。 该设计产生低液压,具有高液体流量,适用于纳米FLUP应用。 证明短填料(2cm C18颗粒)隧道玻璃料柱能够持续10,000psi连续液流超过一周,没有任何颗粒泄漏或压力不稳定性。 隧道玻璃料也成功应用于nanoUPLC捕集和分析柱系统的制造。 已被证明具有高分离效率和敏感性,用于分析胰蛋白酶肽,以及提高磷酸肽分析的检测灵敏度。

    Heparin/heparan sulfate-dependent inhibitors of activated protein C and uses thereof in treating hemophilic disorders
    359.
    发明授权
    Heparin/heparan sulfate-dependent inhibitors of activated protein C and uses thereof in treating hemophilic disorders 有权
    活化蛋白C的肝素/硫酸乙酰肝素依赖性抑制剂及其在治疗嗜血性疾病中的用途

    公开(公告)号:US09206246B2

    公开(公告)日:2015-12-08

    申请号:US14081427

    申请日:2013-11-15

    CPC classification number: C07K14/8114 A61K38/00 C07K14/463

    Abstract: Methods for inhibiting activated protein C (APC) comprising contacting the APC with a Kunitz polypeptide in an amount effective in inhibiting the activity of APC, wherein the Kunitz polypeptide comprises six cysteine residues at positions corresponding to positions 7, 16, 32, 40, 53, and 57 in SEQ ID NO:1, a motif X1GX2CBX′ at positions corresponding to positions 13-18 in SEQ ID NO:1, wherein each of X1 and X2, independently, is any amino acid residue, B is a basic amino acid residue, and X′ is G, A, or V; and at least one heparin-binding motif, which can present at the C-terminus of the Kunitz polypeptide.

    Abstract translation: 抑制活化蛋白C(APC)的方法包括以有效抑制APC活性的量使APC与Kunitz多肽接触,其中Kunitz多肽在对应于7,16,32,40,53位的位置包含6个半胱氨酸残基 ,57个,SEQ ID NO:1中的57个,在对应于SEQ ID NO:1中13-18位的位置上的基序X1GX2CBX',其中X1和X2各自独立地是任何氨基酸残基,B是碱性氨基酸 残基,X'为G,A或V; 和至少一种肝素结合基序,其可以存在于Kunitz多肽的C末端。

    Piezoelectric actuating device
    360.
    发明授权
    Piezoelectric actuating device 有权
    压电驱动装置

    公开(公告)号:US09190938B2

    公开(公告)日:2015-11-17

    申请号:US13784068

    申请日:2013-03-04

    CPC classification number: H02N2/001 H01L41/0973 H02N2/0015 H02N2/0095

    Abstract: A piezoelectric actuating device includes a carrier, at least a piezoelectric unit, at least a linked component and a moving component. The piezoelectric unit is disposed on the carrier and includes at least a piezoelectric buzzer. The linked component is disposed corresponding to the piezoelectric unit. One end of the linked component is attached to the piezoelectric buzzer. The moving component is connected with the linked component. When the piezoelectric buzzer is actuated, it can carry the linked component to move correspondingly so as to move the moving component. The piezoelectric actuating device has the advantage of low cost and can achieve the sub-nanometer scale actuating resolution.

    Abstract translation: 压电致动装置包括载体,至少压电单元,至少一个连接部件和移动部件。 压电单元设置在载体上并且至少包括压电蜂鸣器。 连接部件对应于压电单元设置。 连接部件的一端连接到压电蜂鸣器。 移动组件与链接组件连接。 当压电蜂鸣器被致动时,它可以携带相连的部件相应地移动以移动移动部件。 压电驱动装置具有成本低廉的优点,可实现亚纳米级的致动分辨率。

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