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    • 6. 发明授权
    • Mass spectrometry system and mass spectrometry method
    • 质谱系统和质谱法
    • US07626162B2
    • 2009-12-01
    • US12038829
    • 2008-02-28
    • Shuhei HashibaTakeshi Sakamoto
    • Shuhei HashibaTakeshi Sakamoto
    • B01D59/44H01J49/26H01J49/42
    • H01J49/0027G01N30/724Y10T436/13
    • When a liquid mixture of two samples such as biological samples labeled with stable isotopes is subjected to a relative quantitative analysis using a liquid chromatography-tandem mass spectrometry system, various constituents are simultaneously ionized. Accordingly, sufficient time required for second mass spectrometry is not ensured, whereby some ions remain unanalyzed after measurement. To address this problem, after second mass spectrometry, amino acid sequencing is performed using the analysis data of the second mass spectrometry, which enables determination on the presence/absence of a specific amino acid labeled with a stable isotope. When the specific amino acid is present, the m/z value of an isotopically-labeled-paired ion in an MS spectrum is calculated, and non-target information for use in second mass spectrometry is created using the calculated m/z information. This avoids redundant second mass spectrometry on sample components derived from the same peptide while allowing second mass spectrometry to be efficiently performed.
    • 当使用液相色谱 - 串联质谱系统进行相对定量分析,将诸如用稳定同位素标记的生物样品的两个样品的液体混合物进行相对定量分析时,同时电离各种成分。 因此,不能确保第二质谱所需的足够的时间,从而在测量之后一些离子保持未分析。 为了解决这个问题,在第二次质谱法之后,使用第二质谱分析数据进行氨基酸测序,其能够确定用稳定同位素标记的特定氨基酸的存在/不存在。 当存在特定氨基酸时,计算MS谱中同位素标记配对离子的m / z值,并使用所计算的m / z信息产生用于第二质谱的非目标信息。 这避免了来自相同肽的样品组分的冗余第二质谱,同时允许有效地进行第二质谱。