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Comprehensive Analysis of Glycerophospholipids





 Data                                                                                                                Subcutaneous Tissue  Mass Imaging of
            According to Alzheimer’s Disease International, there were an estimated
            35,600,000 known Alzheimer patients in 2010, world-wide, with the number
 Results from comprehensive analysis of glycerophospholipids are shown in Fig. 1. The first dimension (normal-phase LC) separates   of patients doubling every 20 years. By 2050, the number is expected to
 samples by glycerophospholipid type. The second dimension (reverse-phase LC) separates samples by acyl group chain length. The   increase to an estimated 115,400,000 patients. Biomarkers such as the tau and   Analysis of
 specialized ChromSquare software visually displays data analysis results two-dimensionally. This allows the user to get a broad-based   beta-amyloid concentrations in the cerebrospinal fluid, positron emission   Comprehensive
 understanding of the types and ratios of glycerophospholipids present and the molecular species in each glycerophospholipid.   tomography (PET), and so on are being used for detection of early-stage   Glycerophospholipids
 Therefore, it is ideal for the comprehensive analysis of glycerophospholipids.  Alzheimer’s disease, but use of these means is limited by problems such as
            being invasive, time-consuming, and expensive. Therefore, to search for other
            Alzheimer biomarkers, M. Mapstone, et al, studied use of lipidomics to identify
 PE group
 2D         a pre-clinical stage Alzheimer’s group among a group of elderly subjects with
 18:0p-18:1 PC  normal cognitive abilities.* Their results reported certain phosphatidylcholines
            (PCs), such as PC diacyl(aa) C36:6, PC aa C38:0, PC aa C38:6, PC aa 40:1, PC                           Technology
 18:0-18:1 PC
            aa C40:2, and PC aa C40:6, as potential biomarker candidates.                                            Supercritical Fluid   Lipid Analysis Using
 16:0-16:0 PC
            * Nature Medicine Volume: 20, pp. 415–418 (2014)
 PI group
 PS group
 PC group
 PG group                                                                                                              Analysis of
                  Comprehensive 2D-LC Technology
 1D                                                                                                                  Glycerophospholipids
                                                                             2 nd  dimension column
                                                                                          MS/MS
                                                                Loop A
 Fig. 1   ChromSquare Plot of Phospholipids Two-Dimensionally Separated by Positive-Mode MRM  1 st  dimension column
 A standard sample was prepared with phosphatidylglycerol (PG), phosphatidyl ethanolamine (PE), phosphatidylinositol (PI),   Auto sampler
 phosphatidylserine (PS), and phosphatidylcholine (PC), each at a concentration of 500 µg/L.  1 st  dimension pumps  Blood Serum
 The ESI-positive mode MRM analysis separated the PG, PE, PI, PS, and PC. Results from identifying the molecular species of PC are   Mediators in Human   Analysis of Lipid
 shown in Fig. 1.
 Three compounds in the PC group shown in Fig. 1 were used as the basis for quantitative analysis. The 5-cycle repeatability and   Loop B
 the linearity of six points within the 50 to 5000 µg/L range for the numeric value (blob area) corresponding to the peak volume of
 the applicable compound are indicated in Fig. 2 and Table 1.  2 nd  dimension pumps
                                         Fig. 3   Flow Lines Configuration of the Nexera-e Comprehensive 2D-LC System
 Area
                  For comprehensive 2D-LC analysis, all components separated in the first-dimensional column enter the second-dimensional column   of Glycolipids  Structural Analysis
                  and are analyzed at ultra high speed. Consequently, the comprehensive 2D-LC system allows phospholipids to be comprehensively
                  separated by normal-phase LC in the first dimension, and then separated according to carbon chain length of fatty acids by
                  reverse-phase LC in the second dimension. This makes it possible to fully automate the previously manual process of TLC
                  separation, recovery from TLC plates, and then separation by reverse-phase LC.


 Conc. (µg/L)                                                                                                          Analysis of Fatty Acid
 Fig. 2   Linearity of PC (18:0-18:1)                                                                              Content of Human ES Cells  Composition in Overall Lipid
 Table 1   Retention Time and Area Reproducibility of Five Repetitions for Three PC Components and Linearity of 50 to 5000 µg/L Range

 Compound  MRM transition  Total retention time  Retention time   Blob Area (%RSD)  Correlation
 (%RSD)  (2D)  coef cient (R)
 16:0-16:0 PC  m/z 734.6 > 184.1  0.0072  0.9  6.8  0.999799
 18:0-18:1 PC  m/z 788.6 > 184.1  0.013  1.1  8.9  0.999947  Comprehensive Two-Dimensional Liquid Chromatograph    Esters by GC  Acid Methyl
                                                          Nexera-e                                                     Analysis of Fatty
 18:0p-18:1 PC  m/z 772.6 > 184.1  0.013  1.2  6.4  0.999656

                  Reference: Nexera-e brochure (C190-E172)




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