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    • 2. 发明授权
    • Recognition of oligonucleotides containing non-standard base pairs
    • 识别含有非标准碱基对的寡核苷酸
    • US06037120A
    • 2000-03-14
    • US542142
    • 1995-10-12
    • Steven Albert Benner
    • Steven Albert Benner
    • C07H21/00C12P19/34C12Q1/68C07H21/04
    • C07H21/00C12P19/34C12Q1/68
    • The disclosure describes a new method for intermolecular recognition between two molecules, where complementary oligonucleotide strands bind in aqueous solution, where these strains contain non-standard nucleobases that can pair to fit the Watson-Crick geometry in that they involve a monocyclic six membered ring pairing with a fused bicyclic heterocyclic ring system composed of a five member ring fused with a six membered ring, with the orientation of the heterocycles with respect to each other and with respect to the backbone chain analogous to that found in DNA and RNA, but with a pattern of hydrogen bonds holding the base pair together different from that found in the AT and GC base pairs (a "non-standard base pair").
    • 本公开描述了两种分子之间的分子间识别的新方法,其中互补的寡核苷酸链在水溶液中结合,其中这些菌株含有可以配对以适应沃森 - 克里克几何的非标准核碱基,因为它们涉及单环六元环配对 与由六元环稠合的五元环组成的稠合双环杂环体系,杂环相对于彼此和相对于骨架链的取向类似于在DNA和RNA中发现的杂环,但是具有 将碱基对保持的氢键的模式与AT和GC碱基对(“非标准碱基对”)中发现的不同。
    • 4. 发明授权
    • Inexpensive autonomous assembly of ultra-large (UL) DNA constructs
    • 超大型(UL)DNA构建体的廉价自主装配
    • US09297041B1
    • 2016-03-29
    • US14048671
    • 2013-10-08
    • Steven Albert Benner
    • Steven Albert Benner
    • C12Q1/68C12P19/34
    • C12Q1/6862C12P19/34C12Q2521/501C12Q2525/117
    • This invention provides processes to assemble many (greater than 20) partially overlapping single stranded DNA molecules (fragments) having preselected sequences, followed by extension of those strands that hybridize at terminal overlap regions, and ligation of the extend products, creating a double-stranded DNA assembly. These processes use non-standard nucleotides carrying heterocyclic nucleobase analogs that implement non-standard hydrogen bonding patterns; these allow controlled annealing of the single stranded fragments via Watson-Crick rules, with less or no interference from a range of non-Watson Crick interactions, hairpin formations, or off-target hybridization displayed by standard nucleobases. This process includes an optional conversion step that replaces non-standard nucleobase pairs with standard nucleobase pairs, generating large synthetic DNA (LS-DNA) molecules containing only natural nucleotides. As useful application, this invention allows the assembly of genes encoding whole proteins (typically 1000-3000 nucleotide pairs) from a collection of single stranded DNA fragments at reduced cost and effort.
    • 本发明提供了组装具有预选序列的许多(大于20个)部分重叠的单链DNA分子(片段)的方法,随后延伸在末端重叠区域杂交的那些链,以及延伸产物的连接,产生双链 DNA组装。 这些方法使用携带杂环核苷酸类似物的非标准核苷酸实现非标准氢键合模式; 这些允许通过Watson-Crick规则对单链片段进行受控退火,具有来自非标准核碱基显示的非沃森克里克相互作用,发夹结构或脱靶杂交范围的较少或不受干扰。 该过程包括可选的转化步骤,其用标准核碱基对取代非标准碱基对,产生仅含有天然核苷酸的大合成DNA(LS-DNA)分子。 作为有用的应用,本发明允许以降低的成本和精力从组合的单链DNA片段装配编码全蛋白的基因(通常为1000-3000个核苷酸对)。
    • 5. 发明授权
    • Polymerase incorporation of non-standard nucleotides
    • 聚合酶掺入非标准核苷酸
    • US08614072B2
    • 2013-12-24
    • US12999138
    • 2009-06-16
    • Steven Albert BennerZunyi Yang
    • Steven Albert BennerZunyi Yang
    • C12P19/34C12Q1/68
    • C12Q1/6853C12P19/34C12Q1/686C12Q2521/101C12Q2525/117C12Q2525/191
    • The disclosed invention teaches processes to amplify oligonucleotides by contacting templates and primers with DNA polymerases and triphosphates of non-standard nucleotides, which form nucleobase pairs fitting the standard Watson-Crick geometry, but joined by hydrogen bonding patterns different from those that join standard A:T and G:C pairs. Thus, this invention relates to nucleotide analogs and their derivatives that, when incorporated into DNA and RNA, expand the number of replicatable nucleotides beyond the four found in standard DNA and RNA. The invention further relates to polymerases that incorporate those non-standard nucleotide analogs into oligonucleotide products using the corresponding triphosphate derivatives, and more specifically, polymerases and non-standard nucleoside triphosphates that support the polymerase chain reaction (PCR), including PCR where the products contain more than one non-standard nucleotide unit.
    • 所公开的发明教导了通过使模板和引物与DNA聚合酶和非标准核苷酸的三磷酸接触来扩增寡核苷酸的过程,其形成适合标准Watson-Crick几何形状的核碱基对,但是通过与加入标准A: T和G:C对。 因此,本发明涉及核苷酸类似物及其衍生物,其在掺入DNA和RNA时扩大超出标准DNA和RNA中发现的四种可重复核苷酸的数量。 本发明还涉及使用相应的三磷酸衍生物,更具体地,支持聚合酶链式反应(PCR)的聚合酶和非标准核苷三磷酸(包括产物含有的PCR)的寡核苷酸产物,将这些非标准核苷酸类似物结合到聚合酶中的聚合酶 多个非标准核苷酸单位。
    • 6. 发明授权
    • In vitro selection with expanded genetic alphabets
    • 用扩增的基因字母表进行体外选择
    • US08586303B1
    • 2013-11-19
    • US13493172
    • 2012-06-11
    • Steven Albert BennerZunyi Yang
    • Steven Albert BennerZunyi Yang
    • C12Q1/68C12P19/34
    • C12Q1/6811C12Q2521/345C12Q2525/117C12Q2525/205
    • This invention enables processes for extracting from a mixture of oligonucleotide molecules individuals that bind to a preselected target (aptamers) or catalyze a preselected reaction (xNAzymes) that contain one or more non-standard nucleotides. These pair with their complements in a Watson-Crick geometry with a pattern of hydrogen bonds different from that pairing adenine and thymine, and guanine and cytosine. The processes comprise (a) obtaining this mixture containing non-standard nucleotides within preselected regions, (b) contacting the mixture with a preselected target or one or more reactants for the reaction whose catalysis is desired, (c) separating oligonucleotides having a greater affinity to the target or catalytic effectiveness from the remainder that have less affinity or catalytic effectiveness, and (d) amplifying the separated oligonucleotides. The process exploits PCR conditions that amplify oligonucleotides with less than 5% loss of the non-standard nucleotide per cycle, and processes to determine the sequences of the amplified oligonucleotides.
    • 本发明使得能够从寡核苷酸分子的混合物提取与结合预选靶(适体)的个体或催化包含一个或多个非标准核苷酸的预选反应(xNAzymes)的方法。 这些与他们在沃森 - 克里克几何中的补体配对,具有与该配对腺嘌呤和胸腺嘧啶不同的氢键模式,以及鸟嘌呤和胞嘧啶。 所述方法包括(a)获得在预选区域内含有非标准核苷酸的混合物,(b)使混合物与预选靶物或一种或多种反应物接触,用于需要其催化的反应,(c)分离具有较大亲和力的寡核苷酸 与具有较小亲和性或催化效力的其余部分的靶标或催化有效性,和(d)扩增分离的寡核苷酸。 该过程利用扩增每个周期中非标准核苷酸少于5%的寡核苷酸的PCR条件,以及确定扩增的寡核苷酸序列的方法。
    • 8. 发明授权
    • Chimeras of sulfur-linked oligonucleotide analogs and DNA and RNA
    • 硫链寡核苷酸类似物和DNA和RNA的嵌合体
    • US06444798B1
    • 2002-09-03
    • US08645411
    • 1996-05-13
    • Steven Albert Benner
    • Steven Albert Benner
    • A61K317125
    • C07D473/00C07H19/04C07H21/00
    • This invention dicloses compositions of matter that are oligonucleotide analogs containing one or more improvements, where the improvement consists of replacing one or more of the phosphodiester linking units (—O—PO2−—O—) by a dimethylene sulfide (—CH2—S—CH2—), sulfoxide (—CH2—SO—CH2—), or sulfone linking unit (—CH2—SO2—CH2—). This linkage is stable to degradation both by enzymes and by alkaline hydrolysis, contains no stereogenic atoms, and confers improved stability and the ability to fold into tertiary structure upon natural oligonucleotides and their analogs.
    • 本发明公开了包含一个或多个改进的寡核苷酸类似物的物质组合物,其中改进包括用二亚硫酰基(-CH 2 -S-)代替一个或多个磷酸二酯连接单元(-O-PO 2 -O-) CH2-),亚砜(-CH2-SO-CH2-)或砜连接单元(-CH2-SO2-CH2-)。 这种连接对于通过酶和碱性水解降解是稳定的,不含立体原子,并赋予改进的稳定性和在天然寡核苷酸及其类似物上折叠成三级结构的能力。
    • 9. 发明授权
    • Reagents for reversibly terminating primer extension
    • 可逆终止引物延伸的试剂
    • US08212020B2
    • 2012-07-03
    • US12383306
    • 2009-03-23
    • Steven Albert BennerDaniel HutterNicole Aurora LealFei Chen
    • Steven Albert BennerDaniel HutterNicole Aurora LealFei Chen
    • C07H17/02C07H19/04C07H19/10C07H19/20C07H21/04
    • C07H19/10C07H19/073C07H19/14C07H19/173C07H23/00
    • This invention relates to the field of nucleic acid chemistry, more specifically to the field of compositions of matter that comprise triphosphates of modified 2′-deoxynucleosides and oligonucleotides that are formed when these are appended to the 3′-end of a primer, wherein said modifications comprise NH2 moiety attached to their 3′-hydroxyl group and a fluorescent species in a form of a tag affixed to the nucleobase via a linker that can be cleaved. Such compositions and their associated processes enable and improve the sequencing of oligonucleotides using a strategy of cyclic reversible termination, as outlined in U.S. Pat. No. 6,664,079. Most specifically, the invention concerns compositions of matter that are 5′-triphosphates of ribo- and 2′-deoxyribonucleosides carrying detectable tags and oligonucleotides that might be derived from them. The invention also concerns processes wherein a DNA polymerase, RNA polymerase, or reverse transcriptase synthesizes said oligonucleotides via addition of said triphosphates to a primer.
    • 本发明涉及核酸化学领域,更具体地涉及包含修饰的2'-脱氧核苷的三磷酸的物质组合物领域和当它们附着于引物的3'-末端时形成的寡核苷酸,其中所述 修饰包括连接到它们的3'-羟基上的NH 2部分和通过能够被切割的接头固定在核碱基上的标签形式的荧光物质。 这样的组合物及其相关方法使用循环可逆终止的策略实现和改进了寡核苷酸的测序,如美国专利No. 6,664,079。 最具体地,本发明涉及携带检测标签的核糖核酸和2'-脱氧核糖核苷的5'-三磷酸的物质组合物,所述可检测标签和寡核苷酸可能来源于它们。 本发明还涉及其中DNA聚合酶,RNA聚合酶或逆转录酶通过向引物中加入所述三磷酸合成所述寡核苷酸的方法。
    • 10. 发明申请
    • Formamide-containing mixtures for detecting nucleic acids
    • 用于检测核酸的含甲酰胺的混合物
    • US20110117554A1
    • 2011-05-19
    • US12927430
    • 2010-11-15
    • Steven Albert BennerDaniel HutterNicole A. Leal
    • Steven Albert BennerDaniel HutterNicole A. Leal
    • C12Q1/68
    • C12Q1/6832C12Q2525/113C12Q2527/125
    • Specific sequences of DNA are often detected by a process that comprises a step where the sequence to be detected (the “analyte”) binds to give a duplex with a DNA molecule or analog that is complementary in the Watson-Crick sense to some portion of the analyte in an aqueous “assay environment” that may contain buffer, salt, and/or detergent. Such purely aqueous systems cannot be exposed indefinitely to the environment, however, as the water in the system will evaporate. Further, such systems often support the growth of bacteria and other organisms, destroying their effectiveness. This invention provides for compositions of matter and processes that use them that comprise assay mixtures containing more than 40% formamide. This mixture remains a liquid at equilibrium with water in environments normally inhabited by humans. This invention also provides for mixtures containing formamides that include detergents. Formamide is usually regarded as a denaturant for duplex formation, destabilizing the binding that is key to detection. This invention therefore also provides for materials that form duplexes in formamide-water mixtures.
    • DNA的特定序列通常通过包括待检测序列(“分析物”)结合以产生与Watson-Crick意义上互补的DNA分子或类似物的双链体的方法来检测。 可以含有缓冲液,盐和/或洗涤剂的水性“测定环境”中的分析物。 这种纯水系统不能无限期地暴露于环境中,然而,系统中的水将蒸发。 此外,这种系统通常支持细菌和其他生物的生长,破坏其有效性。 本发明提供了使用它们的物质和方法的组合物,其包含含有超过40%甲酰胺的测定混合物。 该混合物在通常由人类居住的环境中保持与水平衡的液体。 本发明还提供含有包含洗涤剂的甲酰胺的混合物。 甲酰胺通常被认为是双相形成的变性剂,破坏了检测关键的结合。 因此,本发明还提供了在甲酰胺 - 水混合物中形成双链体的材料。