Platform for Native Liquid Chromatography-Mass Spectrometry

    公开(公告)号:US20230266286A1

    公开(公告)日:2023-08-24

    申请号:US18104669

    申请日:2023-02-01

    CPC classification number: G01N30/7266 G01N30/38 G01N30/7273 G01N2030/027

    Abstract: Disclosed are native liquid chromatography-mass spectrometry systems and methods of use. A native liquid chromatography-mass spectrometry system can include a liquid chromatography system capable of separating a sample; and an electrospray ionization mass spectrometry (ESI-MS) system in fluid communication with the liquid chromatography system, wherein the ESI-MS system comprises a multi-nozzle electrospray ionization emitter and a system for modifying a desolvation gas and a mass spectrometer, wherein the mass spectrometer is configured to receive ions and characterize mass to charge ratio of ions.

    PROTEIN N-TERMINAL DE NOVO SEQUENCING BY POSITION-SELECTIVE DIMETHYLATION

    公开(公告)号:US20230032607A1

    公开(公告)日:2023-02-02

    申请号:US17863349

    申请日:2022-07-12

    Abstract: The present invention generally pertains to methods of determining the amino acid sequence of a protein. In particular, the present invention pertains to the use of position-selective dimethylation and liquid chromatography-mass spectrometry to enhance the signal of N-terminal peptides and shift the signal of N-terminal peptides and corresponding b ions, thus facilitating a determination of the sequence of N-terminal peptides.

    Hydrophobic interaction chromatography-coupled native mass spectrometry for antibody analysis

    公开(公告)号:US11525833B2

    公开(公告)日:2022-12-13

    申请号:US17033820

    申请日:2020-09-27

    Abstract: The present invention provides rapid, sensitive high-throughput methods and systems for characterizing peptides or proteins using hydrophobic interaction chromatography-coupled native mass spectrometry to improve manufacturing process of biopharmaceutical products, such as identifying impurities during antibody purification, monitoring post-translational modification variants during production, or characterizing drug-to-antibody ratio of antibody-drug conjugates. The separation profiles of the peptides or proteins are generated and compared to identify or qualify the peptides or proteins.

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