首页> 外国专利> Sequencing nucleic acids for e.g. analyzing genomes, comprises contacting nucleic acid-degrading enzymes with free fluorescent labeled nucleic acids, and determining base sequence

Sequencing nucleic acids for e.g. analyzing genomes, comprises contacting nucleic acid-degrading enzymes with free fluorescent labeled nucleic acids, and determining base sequence

机译:测序核酸例如分析基因组,包括使核酸降解酶与游离的荧光标记核酸接触,并确定碱基序列

摘要

Sequencing (M1) nucleic acids, by: (a) contacting a support having nucleic acid-degrading enzyme molecules, with free nucleic acid molecules carrying fluorescent labeling groups; (b) progressively cleaving off individual nucleotide building blocks from free nucleic acids; and (c) determining sequence of nucleic acids on basis of time-dependent change, in fluorescence of nucleic acid molecules. Sequencing (M1) nucleic acids, comprises: (a) providing a support (2) having a multiplicity of nucleic acid-degrading enzyme molecules (4) immobilized on it, contacting the support with free nucleic acid molecules carrying several fluorescent labeling groups, progressively cleaving off individual nucleotide building blocks from the free nucleic acid molecules by the immobilized enzyme molecules, and simultaneously determining the base sequence of several nucleic acid molecules on the basis of the time-dependent change, caused when nucleotide building blocks are cleaved off, in the fluorescence of the nucleic acid molecules and/or of the cleaved-off nucleotide building blocks; or (b) providing a support having a multiplicity of nucleic acid-polymerizing enzyme molecules immobilized on it, contacting the support with free nucleic acid molecules to which a primer molecule is bound and nucleotide building blocks carrying a fluorescent labeling group, incorporating the nucleotide building blocks into the primer by the immobilized enzyme molecules, and simultaneously determining the base sequence of several nucleic acid molecules on the basis of the time-dependent change, caused when nucleotide building blocks are incorporated, in the fluorescence of the extended primer molecule and/or of the nucleotide building blocks. Independent claims are also included for the following: (1) an apparatus (I) for performing (M1), comprising: (a) a support comprising a multiplicity of enzyme molecules immobilized on it, modes for delivering free nucleic acid molecules carrying several fluorescent labeling groups to the support, or generating free nucleic acid molecules carrying several fluorescent labeling groups on the support, a reaction space for progressively cleaving off individual nucleotide building blocks from the nucleic acid molecules, and mode for determining simultaneously the base sequence of several nucleic acid molecules on the basis of the time-dependent change, caused when nucleotide building blocks are cleaved off, in the fluorescence of the nucleic acid molecules and/or the cleaved-off nucleotide building blocks; or (b) a support comprising a multiplicity of nucleic acid-polymerizing enzyme molecules immobilized on it, modes for providing free nucleic acid molecules to which a primer molecule is bound, and nucleotide building blocks carrying a fluorescent labeling group on the support, a reaction space for incorporating the nucleotide building blocks into the primer, and mode for determining simultaneously the base sequence of several nucleic acid molecules on the basis of the time-dependent change, caused when nucleotide building blocks are incorporated, in the fluorescence of the extended primer molecule and/or of the nucleotide building blocks; (2) studying (M2) enzyme-substrate interactions, comprising providing a support having a multiplicity of enzyme molecules immobilized on it, contacting the support with free substrate molecules carrying fluorescent labeling groups, reacting the substrate molecules with the immobilized enzyme molecules, and studying simultaneously the enzyme-substrate interaction of several individual enzyme and/or substrate molecules on the basis of the time-dependent change, caused during the enzymic reaction of substrate molecules, in the fluorescence of the substrate molecules and/or cleaved-off substrate portions and/or reaction products formed; and (3) an apparatus (II) for performing (M2), comprising a support comprising a multiplicity of enzyme molecules immobilized on it, modes for delivering free substrate molecules carrying fluorescent labeling groups to the support, or generating free substrate molecules carrying fluorescent labeling groups on the support, a reaction space for reacting the substrate molecules with the immobilized enzyme molecules, and mode for studying simultaneously several enzyme-substrate interactions of several enzyme and/or substrate molecules on the basis of the time-dependent change, caused during the enzymic reaction, in the fluorescence of the substrate molecules and/or the cleaved-off substrate portions and/or reaction products formed.
机译:通过以下方式对(M1)核酸进行测序:(a)使具有核酸降解酶分子的支持物与带有荧光标记基团的游离核酸分子接触; (b)从游离核酸中逐步切割出单个核苷酸结构单元; (c)基于时间依赖性的变化,确定核酸分子荧光中的核酸序列。测序(M1)核酸,包括:(a)提供其上固定有多个核酸降解酶分子(4)的支持物(2),使所述支持物与带有几个荧光标记基团的游离核酸分子逐渐接触通过固定的酶分子从游离核酸分子上切下单个核苷酸结构单元,并基于时间依赖性变化同时确定几个核酸分子的碱基序列,所述时间依赖性变化是在核苷酸结构单元被切割时引起的。核酸分子和/或裂解的核苷酸构件的荧光;或(b)提供其上固定有多个核酸聚合酶分子的支持物,使该支持物与结合有引物分子的游离核酸分子和带有荧光标记基团的核苷酸结构单元接触,并结合核苷酸结构通过固定的酶分子在引物中进行阻断,并根据时间依赖性变化同时确定多个核酸分子的碱基序列,所述时间依赖性变化是在核苷酸构建基被掺入时在扩展引物分子和/或荧光中引起的核苷酸构件。还包括以下方面的独立权利要求:(1)用于执行(M1)的设备(I),包括:(a)包含固定在其上的多种酶分子的载体,用于输送带有几种荧光的游离核酸分子的方式标记到支持物上的标记基团,或生成在支持物上带有几个荧光标记基团的游离核酸分子,用于从核酸分子中逐步分离出各个核苷酸构建基的反应空间,以及同时确定多个核酸碱基序列的方式基于时间依赖性变化的分子,所述时间依赖性变化是在核酸分子和/或被切割的核苷酸结构单元的荧光中,当切割核苷酸结构单元时引起的;或(b)包含固定在其上的多种核酸聚合酶分子的载体,提供与引物分子结合的游离核酸分子的方式以及在载体上带有荧光标记基团的核苷酸结构单元的反应用于将核苷酸构件掺入引物中的空间,以及用于在扩展的引物分子的荧光中根据掺入核苷酸构件时引起的时间依赖性变化同时确定多个核酸分子的碱基序列的模式和/或核苷酸构件; (2)研究(M2)酶-底物相互作用,包括提供具有固定在其上的多种酶分子的载体,使载体与带有荧光标记基团的游离底物分子接触,使底物分子与固定的酶分子反应,并研究同时,在底物分子和/或裂解的底物部分的荧光中,基于底物分子的酶促反应期间引起的时间依赖性变化,几个单独的酶和/或底物分子的酶-底物相互作用以及/或形成反应产物; (3)用于进行(M2)的装置(II),其包括:支持物,其包含固定在其上的多种酶分子;将带有荧光标记基团的游离底物分子递送至所述支持物;或产生带有荧光标记的游离底物分子的模式载体上的基团,用于使底物分子与固定的酶分子反应的反应空间,以及根据时间依赖性变化同时研究几种酶和/或底物分子的几种酶-底物相互作用的模式。在底物分子和/或裂解的底物部分和/或形成的反应产物的荧光中进行酶促反应。

著录项

  • 公开/公告号DE102004038359A1

    专利类型

  • 公开/公告日2006-03-16

    原文格式PDF

  • 申请/专利权人 RIGLER RUDOLF;

    申请/专利号DE20041038359

  • 发明设计人 RIGLER RUDOLF;

    申请日2004-08-06

  • 分类号C12Q1/68;

  • 国家 DE

  • 入库时间 2022-08-21 21:20:50

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