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Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892
Section on Molecular Dysmorphology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892
Niemann-Pick disease type C1 (NPC1) is a fatal, neurodegenerative, cholesterol storage disorder. With new therapeutics in clinical trials, there is an urgency to improve diagnostics and monitor therapeutic efficacy with biomarkers. In this study, we sought to define the structure of an unknown lipid biomarker for NPC1 with [M + H]+ ion at m/z 509.3351, previously designated as lysoSM-509. The structure of N-palmitoyl-O-phosphocholineserine (PPCS) was proposed for the lipid biomarker based on the results from mass spectrometric analyses and chemical derivatizations. As no commercial standard is available, authentic PPCS was chemically synthesized, and the structure was confirmed by comparison of endogenous and synthetic compounds as well as their derivatives using liquid chromatography-tandem mass spectrometry (LC-MS/MS). PPCS is the most abundant species among N-acyl-O-phosphocholineserines (APCS), a class of lipids that have not been previously detected in biological samples. Further analysis demonstrated that all APCS species with acyl groups ranging from C14 to C24 were elevated in NPC1 plasma. PPCS is also elevated in both central and peripheral tissues of the NPC1 cat model. Identification of APCS structures provide an opportunity for broader exploration of the roles of these novel lipids in NPC1 disease pathology and diagnosis.
). The impaired lipid trafficking is associated with neuron loss and defective myelination, leading to neuroinflammatory and neurodegenerative disease pathology (
), can only stabilize or slow disease progression, early initiation of treatment prior to onset of neurologically symptomatic disease is essential.
In recent years, diagnosis of NPC1 disease has been greatly facilitated by discovery of sensitive and specific biomarkers that are elevated in blood from NPC patients. The most promising of these include oxysterols (
A new simple and rapid LC-ESI-MS/MS method for quantification of plasma oxysterols as dimethylaminobutyrate esters. Its successful use for the diagnosis of Niemann-Pick type C disease.
Determination of serum cholestane-3beta,5alpha,6beta-triol by gas chromatography-mass spectrometry for identification of Niemann-Pick type C (NPC) disease.
Comprehensive evaluation of plasma 7-ketocholesterol and cholestan-3beta,5alpha,6beta-triol in an Italian cohort of patients affected by Niemann-Pick disease due to NPC1 and SMPD1 mutations.
Niemann-Pick type C-2 disease: identification by analysis of plasma cholestane-3beta,5alpha,6beta-triol and further insight into the clinical phenotype.
LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease.
). The oxysterol, cholestane-3β,5α,6β-triol, is the most widely disseminated biomarker and has been implemented on multiple platforms in ∼50 laboratories worldwide. In combination with genetic analyses, oxysterols have become a first line diagnostic test (
), though application of this biomarker has been limited because its structure is unknown. Herein, we performed structural analysis of lysoSM-509 to show that it is N-palmitoyl-O-phosphocholineserine (PPCS), the most abundant species of a class of lipids, N-acyl-O-phosphocholineserines (APCSs). To the best of our knowledge, this is the first description of this lipid class.
MATERIALS AND METHODS
Human subjects
Human studies adhered to the principles of the Declaration of Helsinki, as well as to Title 45, US Code of Federal Regulations, Part 46, Protection of Human Subjects. Informed consent was obtained from the human subjects or their representatives. NPC1 plasma and dried blood spot samples were obtained from the National Institutes of Health and Rush University Medical Center. All NPC1 and NPC1 carrier dried blood spots were de-identified and collected from previously diagnosed patients and obligate heterozygotes, respectively. Normal plasma and dried blood spots were obtained from anonymized residual samples at St. Louis Children's Hospital. Whole blood, plasma, red blood cells, and white blood cells were collected from four heathy adult volunteers. Collection and analysis of de-identified human samples were approved by the institutional review boards at Washington University, Eunice Kennedy Shriver National Institute of Child Health and Human Development, and Rush University Medical Center.
Experimental animals
BALB/c Npcnih (Npc1−/−) mice were obtained from Jackson Laboratories (Bar Harbor, ME) and were maintained in a breeding colony at Washington University. NPC1 cats were raised in the animal colony of the School of Veterinary Medicine at the University of Pennsylvania under National Institutes of Health and US Department of Agriculture guidelines for the care and use of animals in research. Serum/plasma, liver, and brain samples were collected from 24- to 25-week-old cats and 7-week-old mice. Experimental procedures were approved by the Washington University and University of Pennsylvania Animal Studies Committees and were conducted in accordance with the US Department of Agriculture Animal Welfare Act and the Public Health Service Policy for the Humane Care and Use of Laboratory Animals.
Profiling of lysoSM-509 in human plasma and dried blood spots
lysoSM-509 was extracted from plasma samples (50 μl) and dried blood spot discs (3 mm) and submitted to LC-MS/MS. The detailed protocols are described in the supplemental information.
lysoSM-509 structure identification
LC-HRMS of endogenous lysoSM-509 and synthetic PPCS.
The lysoSM-509 isolated from plasma was reconstituted in methanol and submitted to the LC-high-resolution MS (LC-HRMS) assay described in the supplemental information.
Hydrogen/deuterium exchange experiment.
The hydrogen/deuterium (H/D) exchange experiment of isolated lysoSM-509 was conducted on a Shimadzu Prominence HPLC system coupled with the Applied Biosystems/MDS Sciex 4000QTRAP mass spectrometer operating in positive multiple reaction monitoring (MRM) mode, as described in the supplemental information.
Derivatization.
Derivatization of lysoSM-509, including methyl esterification, acylation, ozonolysis, and alkaline degradation, and LC-MS/MS analysis of derivatized lysoSM-509 and synthetic PPCS are described in the supplemental information.
Synthesis of PPCS, d5-PPCS, and potential precursors for PPCS bioanalysis
N-palmitoyl-l-serine methyl ester (2a).
To a solution of N-succinimidyl palmitate (1.35 g, 3.82 mmol, 1 eq) in dichloromethane (15 ml) was added l-serine methyl ester hydrochloride (1a) (1.23 g, 7.93 mmol, 2.1 eq) and triethylamine (1.21 ml, 8.73 mmol, 2.28 eq), and the mixture was stirred at room temperature overnight. The solution was loaded on a silica column and purified with chromatography (dichloromethane/methanol, 10/1) to give 2a (1.19 g, 87%), mp: 86–87°C. 1H NMR (400 MHz, CDCl3) δ 6.58 (d, J = 6.7 Hz, 1H), 4.51 (dt, J = 3.6, 6.7 Hz, 1H), 3.92 (dd, J = 3.6, 11.1, 1H), 3.86 (d, J = 11.1, 1H), 3.73 (s, 3H), 2.22 (t, J = 6.9 Hz, 2H), 1.64−1.54 (m, 2H), 1.27−1.18 (m, 24H), 0.83 (t, J = 6.9, 3H). 13C NMR (100 MHz, CDCl3) δ 173.98, 171.65, 63.23, 54.59, 52.68, 36.48, 31.82, 29.70, 29.67, 29.66, 29.64, 29.52, 29.37, 29.36, 29.26, 25.59, 22.69, 14.12.
A solution of imidazole (2.38 g, 35 mmol, 25 eq) in dichloromethane (25 ml) was cooled to −10°C, followed by addition of phosphorus trichloride (0.611 ml, 7 mmol, 5 eq) and triethylamine (2.92 ml, 21 mmol, 15 eq). The reaction mixture was stirred for 30 min at −10°C. A solution of compound 2a (500 mg, 1.4 mmol, 1 eq) in dichloromethane (20 ml) was added dropwise to the reaction mixture using a syringe pump over a period of 90 min. After the addition, the mixture was stirred for 40 min further and quenched by addition of water (10 ml). The resulting solution was stirred for an additional period of 5 min. The organic layer was washed with brine (10 ml). The aqueous phase was extracted with tetrahydrofuran until it became a clear solution. The combined organic phases were dried with sodium sulfate and concentrated. The residue was dried over phosphorus pentoxide under high vacuum overnight to give 0.91 g of crude 3a.
A mixture of crude 3a (1.4 mmol, 1 eq) and choline tetraphenylborate (1.18 g, 2.8 mmol, 2 eq) was dried by evaporation with anhydrous pyridine (10 ml). The mixture was dissolved in pyridine (10 ml), and 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (0.775 g, 4.2 mmol, 3 eq) was added. The resulting mixture was stirred for 15 min to give 4a. Iodine (0.427 g, 1.68 mmol, 1.2 eq) dissolved in pyridine (3 ml) and water (0.2 ml) was added and the mixture was stirred for 10 min. The solution was washed with 5% (w/v) aqueous solution of sodium bisulfite until the color faded. The mixture was concentrated to give crude 5a, which was confirmed as PPCS methyl ester by LC-MS/MS. The 5a was completely degraded to decomposition products 1 and 2 by alkaline hydrolysis at room temperature for 60 h.
N-palmitoyl-l-serine tert-butyl ester (2b).
The 2b was prepared as a white solid from N-succinimidyl palmitate (1.3 g, 3.68 mmol, 1 eq), l-serine tert-butyl ester hydrochloride (1b) (1.53 g, 7.73 mmol, 2.1 eq), and triethylamine (1.17 ml, 8.4 mmol, 2.28 eq) according to the procedure described for the preparation of 2a (1.45 g, 99%), mp: 64–65°C. 1H NMR (400 MHz, CDCl3) δ 6.58 (d, J = 6.7 Hz, 1H), 4.51 (dt, J = 3.5, 6.7 Hz, 1H), 3.85 (d, J = 3.5 Hz, 2H), 2.22 (t, J = 6.9 Hz, 2H), 1.66−1.55 (m, 2H), 1.45 (s, 9H), 1.27−1.18 (m, 24H), 0.83 (t, J = 6.9, 3H). 13C NMR (100 MHz, CDCl3) δ 173.82, 169.59, 82.54, 63.71, 55.30, 55.27, 36.47, 31.84, 29.61, 29.58, 29.54, 29.41, 29.28, 29.21, 27.90, 25.53, 22.60, 14.02.
The 3b was prepared from 2b (0.94 g, 2.35 mmol, 1 eq), imidazole (4 g, 58.75 mmol, 25 eq), phosphorus trichloride (1.03 ml, 11.75 mmol, 5 eq), and triethylamine (4.9 ml, 35.25 mmol, 15 eq) according to the procedure described for the preparation of 3a. The crude 3b was used directly in the next step without purification.
The 5b was prepared from crude 3b (prepared as above), choline tetraphenylborate (1.99 g, 4.7 mmol, 2 eq), 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (1.3 g, 7.05 mmol, 3 eq), iodine (0.716 g, 2.82, 1.2 eq), and water (0.4 ml) according to the procedure described for the preparation of 5a. The crude 5b was used directly in the next step without purification.
(S)-N-palmitoyl-O-phosphocholineserine.
A suspension of crude 5b (prepared as above) in trifluoroacetic acid (27 ml) and chloroform (27 ml) was stirred at room temperature for 1 day and evaporated to dryness. The residue was chromatographed on C18 silica (methanol-water, 7/3). The PPCS was further purified with chromatography on silica with chloroform-methanol-water (50:49:1) to give a white solid (225 mg, 19% overall yield from 2b), mp: 220–221°C. 1H NMR (400 MHz, CD3OD) δ 4.87 (s, 1H), 4.36 (d, 1H, J = 1.1 Hz), 4.22 (m, 2H), 4.07 (m, 1H), 3.58 (dd, 2H, J = 4.3, 6.2 Hz), 3.26 (d, 1H, J = 1.1 Hz), 3.17 (s, 9H), 2.22 (t, 2H, J = 7.6 Hz), 1.57 (m, 2H), 1.23 (m, 24H), 0.85 (t, 2H, J = 7.6 Hz). 13C NMR (100 MHz, CD3OD) δ 176.03, 175.64, 68.08, 68.03, 60.58, 60.53, 56.73, 56.63, 54.87, 54.84, 54.80, 37.47, 33.24, 30.97, 30.93, 30.83, 30.72, 30.67, 30.65, 27.03, 23.90, 14.62.
N-d5-palmitoyl-l-serine tert-butyl ester (2c).
The 2c was prepared as a white solid from N-succinimidyl-d5-palmitate (0.67 g, 1.87 mmol, 1 eq), l-serine tert-butyl ester hydrochloride (1b) (0.776 g, 3.93 mmol, 2.1 eq), and triethylamine (0.593 ml, 4.26 mmol, 2.28 eq) according to the procedure described for the preparation of 2a (0.71 g, 93%), mp: 64–65°C. 1H NMR (400 MHz, CDCl3) δ 6.53 (d, J = 6.7 Hz, 1H), 4.53 (dt, J = 3.5, 6.7 Hz, 1H), 3.88 (d, J = 3.5 Hz, 2H), 3.22 (s, br, 1H), 2.23 (t, J = 6.9 Hz, 2H), 1.66−1.56 (m, 2H), 1.47 (s, 9H), 1.27−1.18 (m, 22H). 13C NMR (100 MHz, CDCl3) δ 173.83, 169.58, 82.69, 63.94, 55.35, 36.51, 31.57, 29.63, 29.60, 29.56, 29.43, 29.29, 29.26, 29.21, 27.93, 25.54.
The 3c was prepared from 2c (0.71 g, 1.75 mmol, 1 eq), imidazole (2 g, 29.75 mmol, 25 eq), phosphorus trichloride (0.76 ml, 8.75 mmol, 5 eq), and triethylamine (3.65 ml, 26.25 mmol, 15 eq) according to the procedure described for the preparation of 3a. The crude 3c was used directly in the next step without purification.
The 5c was prepared from crude 3c (prepared as above), choline tetraphenylborate (1.48 g, 3.5 mmol, 2 eq), 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (0.97 g, 5.25 mmol, 3 eq), iodine (0.533 g, 2.1, 1.2 eq), and water (0.4 ml) according to the procedure described for the preparation of 5a. The crude 5c was used directly in the next step without purification.
(S)-N-d5-palmitoyl-O-phosphocholineserine.
The (S)-N-d5-palmitoyl-O-phosphocholineserine (d5-PPCS) was prepared as a white solid from crude 5c (prepared as above), trifluoroacetic acid (20 ml), and chloroform (20 ml) according to the procedure described for the preparation of PPCS (85 mg, 9% overall yield from 2c), mp: 221–223°C. 1H NMR (400 MHz, CD3OD) δ 4.87 (s, 1H), 4.36 (d, 1H, J = 1.1 Hz), 4.22 (m, 2H), 4.07 (m, 1H), 3.58 (dd, 2H, J = 4.3, 6.2 Hz), 3.26 (d, 1H, J = 1.1 Hz), 3.17 (s, 9H), 2.22 (t, 2H, J = 7.6 Hz), 1.57 (m, 2H), 1.23 (m, 22H). 13C NMR (100 MHz, CD3OD) δ 175.98, 174.78, 67.50, 67.44, 60.65, 60.60, 55.88, 55.80, 54.87, 54.83, 54.80, 37.26, 32.95, 30.98, 30.96, 30.83, 30.71, 30.61, 27.05.
Synthesis of N-d5-palmitoylserine (6), N-d5-palmitoylphosphatidylserine [N-d5-palmitoyl 1,2-distearoyl-sn-glycero-3-phospho-l-serine (7)], N-d5-palmitoyl-phytosphingosine phosphocholine (8), N-d5-palmitoyl-phosphoserine (9), and O-phosphocholine-d3-l-serine (10) is described in the supplemental information.
Generation of PPCS in heathy human blood and quantification of PPCS in tissues from NPC animal models
The generation of PPCS in heathy human blood and quantification of PPCS in tissues from NPC animal models are described in the supplemental information.
Profiling of APCS in human plasma
Profiling of APCS in human plasma is described in the supplemental information.
Statistical methods
Normally distributed data were analyzed using Student's t-test or ANOVA. Non-normally distributed data was analyzed using the Mann-Whitney test or the Kruskal-Wallis test.
RESULTS
Elucidation of the structure of lysoSM-509
To elucidate the structure of lysoSM-509, we collected the HPLC fractions containing lysoSM-509 from NPC1 plasma and submitted the material for mass spectrometric analysis and chemical derivatization. As it was difficult to isolate sufficient (at least 10 μg) pure endogenous lysoSM-509 from limited NPC plasma samples for acceptable NMR spectra due to its low abundance and the complex plasma lipid components, NMR analysis was not performed. Our strategy for determination of the structure of lysoSM-509 is outlined in Fig. 1.
Fig. 1Strategy for identification of lysoSM-509 structure. HRMS, high-resolution MS; HRMS/MS, high-resolution MS/MS; HDXMS/MS, H/D exchange MS/MS.
High-resolution mass spectrometric analysis of lysoSM-509 in the positive mode showed an abundant ion at an accurate m/z value of 509.3351 for [M+H]+ corresponding to the formula C24H50O7N2P (calculated mass, 509.3350) with mass errors less than 1 mDa (Fig. 2A). The [M+Na]+ ion at m/z 531.3168 (C24H49O7N2PNa; calculated mass, 531.3170) and the [M+2Na-H]+ ion at m/z 553.2986 (C24H48O7N2PNa2; calculated mass, 553.2989) were also observed in positive mode (Fig. 2A), and the [M-H]− ion at m/z 507.3205 (C24H48O7N2P; calculated mass, 507.3205) appeared in negative mode (Fig. 2B), suggesting that there were two acidic groups in lysoSM-509. The molecular formula C24H50O7N2P indicated that the degree of unsaturation in lysoSM-509 was two.
Fig. 2Identification of the structure of lysoSM-509. A: High-resolution mass spectrum of endogenous lysoSM-509 in positive ion mode. B: High-resolution mass spectrum of endogenous lysoSM-509 in negative ion mode. C: High-resolution product ion spectrum of the [M+H]+ ion of endogenous lysoSM-509. D: High-resolution product ion spectrum of the [M+Na]+ ion of endogenous lysoSM-509. E: High-resolution product ion spectrum of the [M+2Na-H]+ ion of endogenous lysoSM-509. F: High-resolution product ion spectrum of the [M-H]− ion of endogenous lysoSM-509. G: H/D exchange of endogenous lysoSM-509 detected with MRM. The [M-2H+3D]+ ion at m/z 512 shows the maximum intensity. H: Product ion spectrum of the [M+H]+ ion of endogenous lysoSM-509 methyl ester.
The high-resolution and accurate-mass product ion spectrum (Fig. 2C) of the [M+H]+ ion acquired with higher energy collisional dissociation (HCD) contained product ions at m/z 184.0730, 124.9997, 104.1072, and 86.0968, corresponding to protonated phosphocholine (C5H15NO4P+; calculated mass, 184.0733), protonated ethylene phosphate (C2H6O4P+; calculated mass, 124.9998), choline (C5H14NO+; calculated mass, 104.1070), vinyltrimethylammonium (C5H12N+; calculated mass, 86.0964), respectively, indicating that lysoSM-509 contains a phosphocholine group (
). Very low abundant product ions at m/z 326.2697 (C19H36NO3+; calculated mass, 326.2690; resulted from neutral loss of a phosphocholine), m/z 271.1045 (C8H20N2O6P+; calculated mass, 271.1053), and m/z 225.0996 (C7H18N2OP+; calculated mass, 225.0999) were also observed. Fragmentation of the [M+Na]+ and [M+2Na-H]+ ions provided information only related to phosphocholine. The product ions of the [M+Na]+ ion include m/z 472.2430 ([M+Na-N(CH3)3]+, C21H40NO7PNa; calculated mass, 472.2435), m/z 348.2511 ([M+Na-phosphocholine]+, C19H35NO3Na+; calculated mass, 348.2509), m/z 206.0552 ([phosphocholine+Na]+, C5H14NO4PNa+; calculated mass, 206.0553), m/z 146.9819 ([ethylene phosphate+Na]+, C2H5O4PNa+; calculated mass, 146.9818), and m/z 86.0964 (vinyltrimethylammonium, C5H12N+; calculated mass, 86.0964) (Fig. 2D). HCD of the [M+2Na-H]+ ion gave m/z 494.2258 ([M+Na2-H-N(CH3)3]+, C21H39NO7PNa2+; calculated mass, 494.2254), m/z 370.2325 ([M+2Na-H-phosphocholine]+, C19H34NO3Na2+; calculated mass, 370.2329), m/z 228.0370 ([phosphocholine+2Na-H]+, C5H13NO4PNa2+; calculated mass, 228.0372), m/z 206.0553 ([phosphocholine+Na]+, C5H14NO4PNa+; calculated mass, 206.0553), m/z 168.9638 ([ethylene phosphate-H+2Na]+, C2H4O4PNa2+; calculated mass, 168.9637), and m/z 86.0964 (vinyltrimethylammonium, C5H12N+; calculated mass, 86.0964) (Fig. 2E). The HCD spectrum of the [M-H]− ion shows product ions at m/z 324.2551 ([M-H-phosphocholine]−, C19H34NO3−; calculated mass, 324.2544), m/z 280.2653 (C18H34NO−; calculated mass, 280.2646), m/z 237.2228 (C16H29O−; calculated mass, 237.2224), m/z 168.0435 ([phosphocholine-CH3]−, C4H11NO4P−; calculated mass, 168.0435), m/z 122.9856 ([ethylene phosphate-H]−, C2H4O4P−; calculated mass, 122.9856), m/z 96.9699 (H2PO4−; calculated mass, 96.9699), and m/z 78.9592 (PO3−; calculated mass, 78.9591) (Fig. 2F). Although product ions at m/z 271.1045 and 225.0996 from fragmentation of protonated lysoSM-509 and m/z 280.2653 and 237.2228 ions from fragmentation of deprotonated lysoSM-509 provided structural information for other than phosphocholine, the structure of lysoSM-509 could not be assigned without more information.
Although the full mass scan of lysoSM-509 offered a good quality spectrum, the H/D exchange experiment using the full mass scan did not provide sufficient sensitivity as the signals were distributed over additional isotope peaks, and the amount of HPLC-isolated lysoSM-509 was limited. MRM was used to detect the deuterium exchange-associated peaks, in which MRM transitions from deuterium exchanged lysoSM-509 to protonated phosphocholine were used. A number of possible deuterated precursors included [M+H]+ at m/z 509, [M+D]+ at m/z 510, [M-H+2D]+ at m/z 511, [M-2H+3D]+ at m/z 512, [M-3H+4D]+ at m/z 513, and [M-4H+5D]+ at m/z 514. Protonated phosphocholine was used to construct the MRM transitions. There are two labile hydrogens in protonated phosphocholine, and deuterated phosphocholine was also included (supplemental Table S1). The number of exchangeable hydrogens is the difference between the mass of the exchanged peak with maximum intensity and the mass of the [M+D]+ at m/z 510. The [M-2H+3D]+ at m/z 512 showed the maximum intensity, showing that there were two exchangeable protons in lysoSM-509 (Fig. 2G).
Chemical derivatization.
Treatment of lysoSM-509 with HCl in methanol gave a methyl ester with mass upshift of 14 Da (Fig. 2H), suggesting that lysoSM-509 bore a carboxylic group. The fragmentation of the [M+H]+ ion of the methyl ester produced the same product ions as those in lysoSM-509. The toleration of acidic conditions by lysoSM-509 indicated that there were no acid-labile groups, such as a vinyl ether or an imine. No acetylated products were observed when lysoSM-509 was treated with acetic anhydride/pyridine, suggesting that it did not have nucleophiles such as amino and alcohol groups. lysoSM-509 survived the treatment with ozone, suggesting that it lacked a carbon-carbon double bond. Treatment of lysoSM-509 with sodium hydroxide in methanol-water (95:5) led to decomposition. Two decomposition products (decomposition product 1, N-palmitoylserine; decomposition product 2, N-palmitoyl-O-methylserine) were confirmed only after authentic PPCS was synthesized.
Proposed structure of lysoSM-509.
We proposed that the phosphocholine was connected to the other moiety of lysoSM-509 via a phosphate bond, similar to phosphatidylcholine and sphingomyelin, because protonated phosphocholine is also the most abundant product ion in fragmentation of [M+H]+ of phosphatidylcholine and sphingomyelin. Besides the phosphocholine and carboxylic groups, the remaining moiety of lysoSM-509 had a formula of C18H35ON, in which the oxygen and nitrogen were most likely part of an amide bond. The presence of the carboxylic acid and the amide groups in lysoSM-509 was in agreement with the degree of unsaturation of two, no amine or alcohol group, and two exchangeable protons. After assignment of phosphocholine, carboxylic acid, and the amide groups, the remaining C17H34 was composed of saturated alkyl groups. lysoSM-509 was temporarily assigned as PPCS.
The structure of PPCS was supported by the proposed fragmentation pathways to all the product ions from the [M+H]+ ion (Fig. 3A). The m/z 326 ion was formed by intra-molecular attack of the carboxylate to the phosphocholine, resulting in loss of a phosphocholine. Loss of palmitoyl as a ketene gave the m/z 271 ion. The 1,4-elimination led to loss of a CO2 and a palmitaldehyde to yield the m/z 225 ion. The dominant product ion at m/z 184 was generated via six-membered ring H-transfer as a major pathway and 1,2-elimination as a minor pathway, which were supported by the H/D exchange experiment. The m/z 184 ion also was generated from the m/z 271 ion after loss of a CO2 and a vinylamine via 1,4-elimination. Further neutral loss of trimethylamine, metaphosphoric acid, and phosphoric acid from the m/z 184 ion yielded the m/z 125, 104, and 86 ions, respectively.
Fig. 3Proposed fragmentation pathways for PPCS. A: Proposed fragmentation pathway for the [M+H]+ ion. B: Proposed fragmentation pathway for the [M-H]− ion.
Unlike other phosphocholine lipids, such as phosphatidylcholine and sphingomyelin, that produce the [M-15]− ion by neutral loss of CH3X via collisional decomposition of the adduct anion [M+X]− at the orifice, where X can be chloride, formate, and acetate (
), PPCS readily formed the [M-H]− ion due to the carboxylic acid group. The structure of PPCS was also supported by fragmentation of the [M-H]− ion. The 1,2-elimination of a phosphocholine afforded the m/z 324 ion. The 1,4-elimination led to loss of a CO2 and a phosphocholine to yield the m/z 280 ion, which underwent 1,4-elimination of a vinylamine to give the m/z 237 ion. Formation of the m/z 168 ion was probably via attack of methyl on choline by the carboxylate followed by 1,2-elimination to yield demanyl phosphate at m/z 168, from which neutral loss of N-vinyldimethylamine and 2-dimethylaminoethanol gave phosphate (m/z 97) and metaphosphate (m/z 79), respectively. The m/z 123 ion was generated after neutral loss of the lactone and trimethylamine from the [M-H]− ion (Fig. 3B).
Synthesis of PPCS
In order to confirm the structure of PPCS, we devised a synthetic plan to generate PPCS. Accordingly, we prepared N-palmitoyl-l-serine methyl ester (2a) and converted it to N-palmitoyl-O-phosphocholineserine methyl ester (5a) via H-phosphonate intermediates 3a and 4a using a modified literature procedure (
) was used for installation of the H-phosphocholine in 4a. However, base hydrolysis of the methyl ester in 5a led to two decomposition products, N-palmitoylserine (decomposition product 1) and N-palmitoyl-O-methylserine (decomposition product 2), in which the phosphocholine group was lost. Although base hydrolysis of a typical sphingomyelin cleaves the phosphoester bond on the choline side to yield ceramide-1-phosphate (
), the phosphoester bond at the serine side of PPCS was cleaved. This unusual cleavage may be due to the intra-molecular participation of the carboxylate group, which attacks carbon-3 of serine to give a four-membered ring lactone. The lactone was unstable due to ring strain and readily opened by attack of hydroxide and methoxide to afford decomposition products 1 and 2 (Fig. 4B). This issue was addressed in a revised approach, in which the methyl ester-protecting group was changed to a tert-butyl ester. Following the same procedure as for 5a, N-palmitoyl-O-phosphocholineserine tert-butyl ester (5b) was prepared. Removal of the tert-butyl ester in 5b with trifluoroacetic acid afforded PPCS. The crude synthetic intermediates, 3a/b to 5a/b, were used directly in the next step without isolation, which significantly simplified the synthetic procedure. PPCS was purified with reverse phase solid phase extraction followed by chromatography on silica. Similarly, d5-PPCS was also prepared as an internal standard for quantification of PPCS from N-d5-palmitoyl-l-serine tert-butyl ester (2c).
Fig. 4Synthesis of PPCS and d5-PPCS (A) and proposed mechanism for the formation of decomposition products 1 and 2 (B).
The structure of lysoSM-509 was confirmed by comparative LC-MS/MS analysis of endogenous and synthesized authentic compound, its methyl esters, and decomposition products under basic conditions. Endogenous lysoSM-509 (Fig. 5A, B) and its methyl ester (Fig. 5C) showed the same retention time and product ion scan spectra as synthetic PPCS and its methyl ester, respectively. The decomposition products of endogenous lysoSM-509 were detected with MRM of all the abundant product ions from collision-induced dissociation of the decomposition products of synthetic PPCS (supplemental Fig. S1), because they were not sufficiently abundant to provide good quality product ion spectra. The decomposition products of endogenous lysoSM-509 matched with those of synthetic PPCS (Fig. 5D). All of the results verified that lysoSM-509 is PPCS.
Fig. 5Confirmation of the structure of lysoSM-509. A: Chromatograms (detected by product ion scan) and high resolution product ion spectra of the [M+H]+ ions of endogenous lysoSM-509 and synthetic PPCS. B: Chromatograms (detected by product ion scan) and high-resolution product ion spectra of the [M-H]− ions of endogenous lysoSM-509 and synthetic PPCS. C: Chromatograms (detected by product ion scan) and product ion spectra of the [M+H]+ ions of endogenous lysoSM-509 methyl ester and synthetic PPCS methyl ester. D: Decomposition products 1 and 2 from synthetic PPCS and endogenous lysoSM-509. Decomposition product 1 was detected in seven MRM transitions. Decomposition product 2 was detected in three MRM transitions.
To explore the ability of PPCS to serve as a biomarker for newborn screening of NPC1 disease, we compared newborn controls (n = 211), NPC1 carriers (n = 10), and NPC1 subjects (n = 10). Compared with newborn controls, PPCS in dried blood spots from NPC1 subjects was elevated only 2.75-fold with overlap between two groups (Fig. 6A), whereas PPCS was elevated 24-fold in NPC1 plasma compared with control plasma (Fig. 6B). The overlap between PPCS in NPC1 and control dried blood spots has also been reported in an earlier report (
Fig. 6PPCS in dried blood spot and plasma samples and its generation in blood during the drying process. A: PPCS in newborn control (n = 211), NPC1 carrier (n = 10), and NPC1 (n = 10) dried blood spot samples. Data are presented as mean ± 95% confidence interval (CI) concentration. P < 0.0001 for lysoSM-509 in NPC1 versus controls and NPC1 carriers. B: PPCS in control (n = 25) and NPC1 (n = 26) plasma samples. Data are presented as mean ± 95% CI peak area. P < 0.0001 for lysoSM-509 in NPC1 versus controls. C: Elevation of PPCS in dried blood spots (n = 5) compared with whole blood (n = 5). The dried blood spots and whole blood from the same subject are shown in the same color. Data are presented as mean ± 95% CI. P < 0.0001 for dried blood spots versus whole blood. D: Elevation of PPCS in dried red blood cell spots (n = 4) compared with red blood cells (n = 4). The dried red blood cell spots and red blood cells from the same subject are shown in the same color. Data are presented as mean ± 95% CI. P < 0.0001 for dried red blood cell spots versus red blood cells. E: Elevation of PPCS in dried white blood cell spots (n = 4) compared with white blood cells (n = 4). The dried white blood cell spots and white blood cells from the same subject are shown in the same color. Data are presented as mean ± 95% CI. P < 0.0001 for dried white blood cell spots versus white blood cells. F: Elevation of PPCS in dried plasma spots (n = 4) compared with plasma (n = 4). The dried plasma spots and plasma from the same subject are shown in the same color. Data are presented as mean ± 95% CI. P < 0.0001 for dried plasma spots versus plasma.
PPCS in blank Whatman 903 newborn screening cards was undetectable. To investigate the basis of attenuated PPCS in dried blood spots compared with plasma, we examined PPCS in whole blood and dried blood spots from the same normal subjects. Compared with whole blood, PPCS in dried blood spots increased 8.3-fold (Fig. 6C). To determine whether components in the Whatman 903 newborn screening card promoted PPCS production in whole blood, we agitated whole blood with 3 mm disks from a blank newborn screening card for 18 h at room temperature. The PPCS levels in blood with newborn screening card disks did not change (not shown), suggesting that PPCS was generated during the drying process. We further compared the PPCS in red blood cells, white blood cells, and plasma with dried red blood cell spots, dried white blood cell spots, and dried plasma spots, respectively. Although PPCS was not detectable in red blood cells and white blood cells, PPCS levels in dried red blood cell spots and white blood cell spots ranged from 60 to 83 ng/ml red blood cells and from 62 to 72 ng/dried white blood cells from 3 ml whole blood, respectively (Fig. 6D, E). Similarly, PPCS in dried plasma spots increased 4-fold compared with plasma levels (Fig. 6F). These results indicate that a PPCS precursor is present in all the blood components and can be converted into PPCS during drying.
We spiked several potential precursors to explore the biosynthetic route of the PPCS, including N-d5-palmitoylserine (6), N-d5-palmitoylphosphatidylserine [N-d5-palmitoyl 1,2-distearoyl-sn-glycero-3-phospho-l-serine (7)], N-d5-palmitoyl-phytosphingosine phosphocholine (8), N-d5-palmitoyl-phosphoserine (9), O-phosphocholine-d3-l-serine (10), and d5-palmitic acid (11) into blood and prepared dried blood spots. However, neither d5-PPCS nor d3-PPCS was observed in the dried blood spots, indicating that none of these compounds appeared to be direct precursors of PPCS (Fig. 7).
Fig. 7Hypothetical pathways for the formation of PPCS. Neither d5-PPCS nor d3-PPCS were formed in dried blood spots from potential precursors, including N-d5-palmitoylserine (6), N-d5-palmitoylphosphatidylserine (N-d5-palmitoyl 1,2-distearoyl-sn-glycero-3-phospho-l-serine) (7), N-d5-palmitoyl-phytosphingosine phosphocholine (8), N-d5-palmitoyl-phosphoserine (9), O-phosphocholine-d3-l-serine (10), and d5-palmitic acid (11).
Elevation of PPCS in serum, brain, and liver from a NPC1 cat model
To understand whether PPCS is elevated in the central nervous system or peripheral organs in NPC1 disease, we analyzed plasma/serum, brain, and liver from NPC1 mouse and cat models. While PPCS was undetectable in plasma and tissues from mouse (data not shown), it was significantly elevated in serum, brain, and liver in NPC1 cats compared with control and NPC1 carrier cats (Fig. 8). This result demonstrated that PPCS accumulates in both central and peripheral tissues and highlighted the species difference between mouse and cat/human with respect to metabolic pathways involved in generation of PPCS.
Fig. 8Elevation of PPCS in serum, brain, and liver from NPC1 cat model. A: PPCS in sera from control (n = 8), NPC1 carrier (n = 3), and NPC1 (n = 7) cats. Data are presented as mean with SD. P < 0.0001 for NPC1 versus control and NPC carriers. B: PPCS in livers from control (n = 9), NPC1 carrier (n = 5), and NPC1 (n = 5) cats. Data are presented as mean with SD. P < 0.0001 for NPC1 versus control and NPC carriers. C: PPCS in brains from control (n = 10), NPC1 carrier (n = 5), and NPC1 (n = 6) cats. Data are presented as mean with SD. P < 0.0001 for NPC1 versus control and NPC carriers.
The structure of PPCS [APCS(16:0)] suggested that it was one of multiple species in the APCS lipid family. We also analyzed other species in plasma using MRM transitions from theoretical masses of [M+H]+ ions of APCS to m/z 184 (Table 1). The APCS species included N-myristoyl- [APCS(14:0)], N-palmitoyl- [APCS(16:0)], N-palmitoleoyl- [APCS(16:1)], N-stearoyl- [APCS(18:0)], N-oleoyl- [APCS(18:1)], N-arachidoyl- [APCS(20:0)], N-behenoyl- [APCS(22:0)], N-lignoceroyl- [APCS(24:0)], and tetracosenoyl-O-phophocholineserines [APCS(24:1)]. Like PPCS, all other APCS species were elevated in NPC1 plasma (Fig. 9).
Fig. 9APCS in human plasma. APCS including N-myristoyl- (APCS(14:0)), N-palmitoyl- [APCS(16:0)], N-palmitoleoyl- [APCS(16:1)], N-stearoyl- [APCS(18:0)], N-oleoyl- [APCS(18:1)], N-arachidoyl- [APCS(20:0)], N-behenoyl- [APCS(22:0)], N-lignoceroyl [APCS(24:0)], and tetracosenoyl-O-phophocholineserines [APCS(24:1)] in control (n = 25) and NPC1 (n = 26) plasma samples. Data are presented as mean ± 95% CI peak area. P < 0.0001 for all APCS species in NPC1 versus controls.
Diagnosis of NPC1 disease is challenging due to the rare nature of the disorder, the genetic heterogeneity, and the initially nonspecific clinical presentation. The advent of NPC1 disease-specific biochemical markers has shortened the time to diagnosis of patients with a high clinical suspicion of NPC1, in which the disease is significantly advanced. Nonetheless, biomarkers that can be applied to the general population or for newborn screening could further improve early identification of the disease. One such marker, lysoSM-509, is currently under evaluation as a NPC1 diagnostic marker (
LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease.
). However, quantification of lysoSM-509 using these assays has not been reliable due to lack of information regarding the molecular identity of the biomarker. As no authentic standard was available, lysosphingomyelin was used as a calibrator. The mass spectrometric responses of lysoSM-509 and lysosphingomyelin and their matrix effects are different, and it is always best to use a chemically identical but isotopically substituted lysoSM-509 internal standard. In the present study, we identified the structure of lysoSM-509 by accurate mass measurements, tandem mass spectra, chemical derivatization, and comparison to an authentic synthetic standard. Unexpectedly, we found that lysoSM-509 is not a lysosphingomyelin species, as previously proposed (
). Rather, the biomarker is PPCS, a member of a unique class of lipids designated as APCS. With the structure of lysoSM-509 in hand, it is now possible to synthesize and use a proper internal standard for its accurate quantification.
To the best of our knowledge, APCS lipids have not previously been described. A series of related serine compounds have been reported in biological samples, including O-serine phosphoethanolamine (
). Later, N-acyl phosphatidylserines and N-acylserines were identified in human brain with the palmitoyl and stearoyl forms being most abundant when analyzed by MS, and their levels change in the frontal cortex in schizophrenia (
). N-acyl lysophosphatidylserines were identified in mouse brain with mass spectrometric lipidomics, and ABHD4 is a general N-acyl phospholipid hydrolase to convert N-acyl phosphatidylserines to N-acyl lysophosphatidylserines (
). O-phosphocholine-l-serine has not been reported previously, and we synthesized O-phosphocholine-d3-l-serine (10) as a potential precursor to study biosynthesis of PPCS in this study.
Although we observed artifactual generation of PPCS in blood components from normal subjects, including whole blood, red blood cells, white blood cells, and plasma, when they were dried on newborn screening cards, PPCS is an endogenous lipid that is stable in blood and plasma under normal experimental conditions. The PPCS level in whole blood did not change at room temperature after the blood was agitated with 3 mm disks from a blank newborn screening card for 18 h. We also developed a validated plasma assay for PPCS that will be published in a separate article, and found that the PPCS level in plasma was unchanged at room temperature for 24 h. Artifactual generation of PPCS in blood on newborn screening cards significantly reduced the difference in PPCS levels between NPC1 and normal subjects. As a result, we observed significant overlap between NPC1 and newborn controls, consistent with an earlier report (
), thus rendering PPCS of limited utility for NPC newborn screening based on detection of the metabolite in dried blood spots. Although our effort to elucidate the biosynthesis of APCS using blood drying on newborn screening cards in this study was not successful, our work has eliminated a number of possibilities and provided a foundation for future study. Understanding the biosynthesis and regulation of APCS and its involvement in NPC and acid sphingomyelinase deficiency, in which plasma PPCS levels are increased (
), may uncover the potential therapeutic targets for these two storage diseases.
Acknowledgments
The authors would like to thank Dr. Douglas Covey for helpful discussion of the synthesis of PPCS. The authors are grateful to the National Niemann-Pick Disease Foundation for their assistance in obtaining samples from NPC1 and NPC1 carrier subjects and express their appreciation to the families and patients who participated in this study.
A new simple and rapid LC-ESI-MS/MS method for quantification of plasma oxysterols as dimethylaminobutyrate esters. Its successful use for the diagnosis of Niemann-Pick type C disease.
Determination of serum cholestane-3beta,5alpha,6beta-triol by gas chromatography-mass spectrometry for identification of Niemann-Pick type C (NPC) disease.
Comprehensive evaluation of plasma 7-ketocholesterol and cholestan-3beta,5alpha,6beta-triol in an Italian cohort of patients affected by Niemann-Pick disease due to NPC1 and SMPD1 mutations.
Niemann-Pick type C-2 disease: identification by analysis of plasma cholestane-3beta,5alpha,6beta-triol and further insight into the clinical phenotype.
LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease.
This work was supported by National Institutes of Health Clinical and Translational Science Award UL1 TR000448 (X.J.) and Grants R01 NS081985 (D.S.O. and J.E.S.), P41-GM103422 (F-F.H), and 2R01DK067859 (M.H.G.); grants from the University of Pennsylvania Orphan Disease Center (X.J.), Dana's Angels Research Trust (D.S.O. and N.M.Y.), and Ara Parseghian Medical Research Foundation (D.S.O. and N.M.Y.); support from Accelerated Research for NPC Disease (D.S.O.), Hope for Hayley and Samantha's Search for the Cure Funds (E.B.K.), and Referral Center for Animal Models of Human Genetic Disease (National Institutes of Health Grant P40 OD010939; C.H.V.). This study was also supported by the intramural research program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (F.D.P.) and a Bench to Bedside Award from the Office of Rare Diseases (F.D.P. and D.S.O.). This work was performed in the Metabolomics Facility at Washington University (National Institutes of Health Grant P30 DK020579). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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