Labeling reagent and methods of use
    74.
    发明申请
    Labeling reagent and methods of use 审中-公开
    标签试剂和使用方法

    公开(公告)号:US20030228700A1

    公开(公告)日:2003-12-11

    申请号:US10289009

    申请日:2002-11-05

    Applicant: IRM LLC

    Abstract: The present invention provides compounds which are useful as multifunctional labels in proteomics studies. The labels of the present invention are both lysine specific and increase the overall sequence coverage obtained in polypeptide mapping experiments, by for example, increasing the ionization efficiencies of lysine-terminated tryptic fragments. In certain aspects, the labels of the present invention can be used to measure differential quantitation, as for example, deuterium(s) can easily be introduced during their synthesis. In one aspect, a C-terminal derivatized lysine biases the fragment ion intensities strongly toward C-terminal fragment ions, resulting in a highly simplified tandem mass spectrum. In further aspects, the number of lysine residues can be determined in a polypeptide.

    Abstract translation: 本发明提供在蛋白质组学研究中可用作多功能标记的化合物。 本发明的标记物都是赖氨酸特异性的,并且通过例如提高赖氨酸终止的胰蛋白酶片段的离子化效率来增加多肽测绘实验中获得的整体序列覆盖率。 在某些方面,本发明的标记可以用于测量差异定量,例如,在合成过程中可以容易地引入氘。 在一个方面,C末端衍生的赖氨酸强烈地将片段离子强度偏向C末端片段离子,导致高度简化的串联质谱。 在另外的方面,可以在多肽中确定赖氨酸残基的数目。

    Liquid chromatography/fourier-transform mass spectrometry/electron capture dissociation for the analysis of proteins
    77.
    发明申请
    Liquid chromatography/fourier-transform mass spectrometry/electron capture dissociation for the analysis of proteins 审中-公开
    液相色谱/傅立叶变换质谱/电子捕获离解用于蛋白质分析

    公开(公告)号:US20030104483A1

    公开(公告)日:2003-06-05

    申请号:US10301110

    申请日:2002-11-21

    Abstract: ECD (Electron Capture Dissociation) FTMS (Fourier-Transform Mass Spectrometry) induced fragmentation is employed to generate sequence information for a protein enzymatic digest. The digest is initially separated by liquid chromatography, e.g., reversed phase nullHPLC, and then ionized nullon-linenull. The ions thus formed may be accumulated in the interface hexapole prior to injection and trapping in the FTMS cell. Typically, no parent ion isolation is performed. The trapped ions are subjected to a pulse of electrons to induce fragmentation. Broad band spectra are acquired continuously to produce a three-dimensional LC/MS data set. The spectra are dominated by c and to a lesser degree z ions, which provide nearly complete sequence coverage. External calibration provides good mass accuracy and resolution, typical of FTMS. Thus, LC/ECD-FTMS is shown to be a highly informative method for the analysis of enzymatic protein digests.

    Abstract translation: 使用ECD(电子俘获解离)FTMS(傅里叶变换质谱)诱导的片段化产生蛋白酶消化的序列信息。 消化液最初通过液相色谱分离,例如反相muHPLC,然后电离“在线”。 这样形成的离子可以在注入之前积聚在界面六极中并在FTMS单元中捕获。 通常,不进行母离子隔离。 被俘获的离子受到电子脉冲的诱导分裂。 连续获取宽带光谱以产生三维LC / MS数据集。 光谱由c和较少的z离子支配,其提供几乎完整的序列覆盖。 外部校准提供了良好的质量精度和分辨率,典型的FTMS。 因此,LC / ECD-FTMS被证明是用于分析酶蛋白质消化的高度信息的方法。

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