Stattic biological activity Usually identified in MS as either the ammonium adduct [M + NH4 ]+ or alkali metal adducts ([M + Na]+ or [M + Li]+ ), while SQDG are mainly detected as negative ions [M ?H]?(Table 2). In order to get details on the structure of lipid molecular species, it is necessary to get additional information by tandem mass spectrometry (MS/MS) studies of each ion observed in MS spectra. Information gathered from MS/MS data and the identification of the typical fragmentation pathways of each lipid class allows several conclusions to be made about the structure of A-836339 web analyzed PLs or GLs, including the identification of the polar head group, the identification of the fatty acyl chains and their location at sn-1 versus sn-2 positions [128]. The typical MS/MS spectra of the [M + H]+ ions of PC, LPC and SM contain a specific product ion of the polar head at m/z 184 (H2 PO4 (CH2 )2 N+ (CH3 )3 . The MS/MS spectra of the [M + Na]+ ions of PC and lysoPC show a neutral loss (NL) of 59 Da, due to the loss of the triethylamine from the head group ( + (CH3 )3 ), loss of 183 Da (HPO4 (CH2 )2 N+ (CH3 )3 ) and loss of 205 Da (NaPO4 (CH2 )2 N+ (CH3 )3 ). PC and LPC can also be analyzed in negative-ion mode as acetate adducts [M + CH3 COO]?. The MS/MS spectra of these ions show a NL 74 Da, due to the loss of CH3 COOCH3 , corresponding to the combined loss of acetate (?9 Da) plus demethylation (?5 Da) of the choline residue and formation of the dimethylamino residue [128?30]. Typical MS/MS spectra of [M ?H]?ions of PI and lysoPI showed the specific product ion at m/z 241 a correspondent to an inositol-1,2-cyclic phosphate anion [128]. Other ions observed at m/z 223 ([C6 H8 PO7 ]?), 297 ([C9 H16 PO10 ]?) and 315 ([C9 H16 PO10 ]?) are also characteristic of PI class [128,131]. PG is also detected as [M ?H]?ions and their MS/MS spectra show a typical product ion at m/z 171 ([C3 H7 O2 OPO3 H]?) as well as the NL of 74 Da ( 3 H6 O2 ,) [128,132]. Although PE and lysoPE can be analyzed in both positive and negative mode, the fragmentation in positive ions is more elucidative for assigning these PL classes. The tandem mass spectra of PE [M + H]+ is dominated by an abundant product ion formed by the NL of 141 Da, which corresponds to elimination phosphoethanolamine head group. The MS/MS of the PE [M + Na]+ ions show a predominant NL of aziridine moiety from the PE polar head group (43 Da) [128]. The MS/MS of PE [M ?H]?ion showed the carboxylate anions R1 COO?and R2 COO?that allow for the pinpointing of the FA composition. PS’s can form positive and negative ions; however, PS negative ions [M ?H]?tend to dominate. The MS/MS spectra of PS [M ?H]?ions yield abundant product ions that correspond to the NL ofMar. Drugs 2016, 14,16 ofserine head group (87 Da). In the MS/MS of PS [M + H]+ ions, the most abundant ion results from loss of the polar head group (185 Da) [133,134]. The fragmentation under MS/MS of [M + Na]+ of neutral glycolipids MGDG and DGDG usually includes the loss of one hexose residue (NL of 162 Da) and, in the case of DGDG, the loss of two hexose residues (NL of 324 Da). The presence of ions at m/z 347 [Hex2res + Na]+ and m/z 365 [Hex2 + Na]+ , as well as the ion at m/z 405 corresponding to the digalactosyl glycero head group [C15 H26 O11 + Na]+ , confirms the presence of the digalactosyl head group [44,135,136]. The typical fragmentation under MS/MS of [M ?H]?ions of SQDG shows the presence of ions at m/z 225 corresponding to the sulfoquinovosyl group, confirming t.Usually identified in MS as either the ammonium adduct [M + NH4 ]+ or alkali metal adducts ([M + Na]+ or [M + Li]+ ), while SQDG are mainly detected as negative ions [M ?H]?(Table 2). In order to get details on the structure of lipid molecular species, it is necessary to get additional information by tandem mass spectrometry (MS/MS) studies of each ion observed in MS spectra. Information gathered from MS/MS data and the identification of the typical fragmentation pathways of each lipid class allows several conclusions to be made about the structure of analyzed PLs or GLs, including the identification of the polar head group, the identification of the fatty acyl chains and their location at sn-1 versus sn-2 positions [128]. The typical MS/MS spectra of the [M + H]+ ions of PC, LPC and SM contain a specific product ion of the polar head at m/z 184 (H2 PO4 (CH2 )2 N+ (CH3 )3 . The MS/MS spectra of the [M + Na]+ ions of PC and lysoPC show a neutral loss (NL) of 59 Da, due to the loss of the triethylamine from the head group ( + (CH3 )3 ), loss of 183 Da (HPO4 (CH2 )2 N+ (CH3 )3 ) and loss of 205 Da (NaPO4 (CH2 )2 N+ (CH3 )3 ). PC and LPC can also be analyzed in negative-ion mode as acetate adducts [M + CH3 COO]?. The MS/MS spectra of these ions show a NL 74 Da, due to the loss of CH3 COOCH3 , corresponding to the combined loss of acetate (?9 Da) plus demethylation (?5 Da) of the choline residue and formation of the dimethylamino residue [128?30]. Typical MS/MS spectra of [M ?H]?ions of PI and lysoPI showed the specific product ion at m/z 241 a correspondent to an inositol-1,2-cyclic phosphate anion [128]. Other ions observed at m/z 223 ([C6 H8 PO7 ]?), 297 ([C9 H16 PO10 ]?) and 315 ([C9 H16 PO10 ]?) are also characteristic of PI class [128,131]. PG is also detected as [M ?H]?ions and their MS/MS spectra show a typical product ion at m/z 171 ([C3 H7 O2 OPO3 H]?) as well as the NL of 74 Da ( 3 H6 O2 ,) [128,132]. Although PE and lysoPE can be analyzed in both positive and negative mode, the fragmentation in positive ions is more elucidative for assigning these PL classes. The tandem mass spectra of PE [M + H]+ is dominated by an abundant product ion formed by the NL of 141 Da, which corresponds to elimination phosphoethanolamine head group. The MS/MS of the PE [M + Na]+ ions show a predominant NL of aziridine moiety from the PE polar head group (43 Da) [128]. The MS/MS of PE [M ?H]?ion showed the carboxylate anions R1 COO?and R2 COO?that allow for the pinpointing of the FA composition. PS’s can form positive and negative ions; however, PS negative ions [M ?H]?tend to dominate. The MS/MS spectra of PS [M ?H]?ions yield abundant product ions that correspond to the NL ofMar. Drugs 2016, 14,16 ofserine head group (87 Da). In the MS/MS of PS [M + H]+ ions, the most abundant ion results from loss of the polar head group (185 Da) [133,134]. The fragmentation under MS/MS of [M + Na]+ of neutral glycolipids MGDG and DGDG usually includes the loss of one hexose residue (NL of 162 Da) and, in the case of DGDG, the loss of two hexose residues (NL of 324 Da). The presence of ions at m/z 347 [Hex2res + Na]+ and m/z 365 [Hex2 + Na]+ , as well as the ion at m/z 405 corresponding to the digalactosyl glycero head group [C15 H26 O11 + Na]+ , confirms the presence of the digalactosyl head group [44,135,136]. The typical fragmentation under MS/MS of [M ?H]?ions of SQDG shows the presence of ions at m/z 225 corresponding to the sulfoquinovosyl group, confirming t.