Phosphorylated glycosphingolipids essential for cholesterol mobilization in C. elegans

Similar documents
Shotgun Proteomics MS/MS. Protein Mixture. proteolysis. Peptide Mixture. Time. Abundance. Abundance. m/z. Abundance. m/z 2. Abundance.

Characterization of an Unknown Compound Using the LTQ Orbitrap

High-sensitivity Orbitrap mass analysis of intact macromolecular assemblies. R. J. Rose, E. Damoc, E. Denisov, A. Makarov, A. J. R.

Supplementary Figure 1 (previous page). EM analysis of full-length GCGR. (a) Exemplary tilt pair images of the GCGR mab23 complex acquired for Random

Supporting information

LOCALISATION, IDENTIFICATION AND SEPARATION OF MOLECULES. Gilles Frache Materials Characterization Day October 14 th 2016

Rapid, Simple Impurity Characterization with the Xevo TQ Mass Spectrometer

Iron depletion enhances production of antimicrobials by Pseudomonas

Advances in Hybrid Mass Spectrometry

Time (min) Supplementary Figure 1: Gas decomposition products of irradiated DMC.

Essential Lipidomics Experiments using the LTQ Orbitrap Hybrid Mass Spectrometer

Relative Quantitation of Human Polymorphonuclear Leukocyte Cell Membrane GPEtn Lipids

Don t miss a thing on your peptide mapping journey How to get full coverage peptide maps using high resolution accurate mass spectrometry

Applying a Novel Glycan Tagging Reagent, RapiFluor-MS, and an Integrated UPLC-FLR/QTof MS System for Low Abundant N-Glycan Analysis

The use of mass spectrometry in lipidomics. Outlines

O O H. Robert S. Plumb and Paul D. Rainville Waters Corporation, Milford, MA, U.S. INTRODUCTION EXPERIMENTAL. LC /MS conditions

Using Multiple Mass Defect Filters and Higher Energy Collisional Dissociation on an LTQ Orbitrap XL for Fast, Sensitive and Accurate Metabolite ID

Glycerolipid Analysis. LC/MS/MS Analytical Services

Comprehensive Lipidome Analysis by Shotgun Lipidomics on a Hybrid Quadrupole-Orbitrap-Linear Ion Trap Mass Spectrometer

SUPPLEMENTARY DATA. Materials and Methods

MASS SPECTROMETRY BASED METABOLOMICS. Pavel Aronov. ABRF2010 Metabolomics Research Group March 21, 2010

NIH Public Access Author Manuscript J Proteome Res. Author manuscript; available in PMC 2014 July 05.

Supporting Information. Lysine Propionylation to Boost Proteome Sequence. Coverage and Enable a Silent SILAC Strategy for

Supporting information for. Determination of sub nm levels of low molecular mass (LMM) thiols in natural waters by liquid

Supplemental Information. LipiDex: An Integrated Software Package. for High-Confidence Lipid Identification

Amadeo R. Fernández-Alba

Quantification of PtdInsP 3 molecular species in cells and tissues by mass spectrometry

Identification of Steroids in Water by Ion Trap LC/MS/MS Application

Analysis of Glycopeptides Using Porous Graphite Chromatography and LTQ Orbitrap XL ETD Hybrid MS

Impact of Chromatography on Lipid Profiling of Liver Tissue Extracts

Determination of red blood cell fatty acid profiles in clinical research

Thermo Scientific LipidSearch Software for Lipidomics Workflows. Automated Identification and Relative. Quantitation of Lipids by LC/MS

Tandem mass spectrometry analysis of prostaglandins and isoprostanes

Lipids Analysis. Lipids

Comparison of Relative Quantification of Monoclonal Antibody N-glycans Using Fluorescence and MS Detection

Selective phosphatidylcholine double bond. fragmentation and localization using. Paternó-Büchi reactions and ultraviolet.

application Natural Food Colorants Analysis of Natural Food Colorants by Electrospray and Atmospheric Pressure Chemical Ionization LC/MS

Profiling Flavonoid Isomers in Highly Complex Citrus Juice Samples Using UPLC Ion Mobility Time-of-Flight Mass Spectrometry

Dr. Erin E. Chambers Waters Corporation. Presented by Dr. Diego Rodriguez Cabaleiro Waters Europe Waters Corporation 1

SWATH Acquisition Enables the Ultra-Fast and Accurate Determination of Novel Synthetic Opioids

PTM Discovery Method for Automated Identification and Sequencing of Phosphopeptides Using the Q TRAP LC/MS/MS System

Increased Identification Coverage and Throughput for Complex Lipidomes

Supplementary Note 1: Interpretation of the proposed mechanisms for the main dissociative

ION MOBILITY COUPLED TO HIGH RESOLUTION MASS SPECTROMETRY: THE POSSIBILITIES, THE LIMITATIONS

Supplementary Information

Quantification with Proteome Discoverer. Bernard Delanghe

Characterization of Disulfide Linkages in Proteins by 193 nm Ultraviolet Photodissociation (UVPD) Mass Spectrometry. Supporting Information

New Instruments and Services

[ APPLICATION NOTE ] APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS KEYWORDS

Supplemental Data. Deinlein et al. Plant Cell. (2012) /tpc

Mass-Spectrometric Analysis of Lipids (Lipidomics)

Nature Biotechnology: doi: /nbt Supplementary Figure 1

Supplementary Figure 1. ESI/MS/MS analyses of native and de-acetylated S2A Supplementary Figure 2. Partial 1D 1H NMR spectrum of S2A

MS/MS Scan Modes. Eötvös University, Budapest April 16, MS/MS Scan Modes. Árpád Somogyi. Product Ion Scan Select. Scan. Precursor Ion Scan Scan

Choosing the metabolomics platform

Profiling of Histone Post-translational Modifications in Mouse Brain with High Resolution Top Down Mass Spectrometry

Development of a Bioanalytical Method for Quantification of Amyloid Beta Peptides in Cerebrospinal Fluid

Supplemental Material. Results

Go beyond. to realities unexplored. Comprehensive workflows, integrated solutions

Application of LC/Electrospray Ion Trap Mass Spectrometry for Identification and Quantification of Pesticides in Complex Matrices

The Comparison of High Resolution MS with Triple Quadrupole MS for the Analysis of Oligonucleotides

NON TARGETED SEARCHING FOR FOOD

Lecture 3. Tandem MS & Protein Sequencing

Rapid and Sensitive Screening of Benzodiazepines in Serum Using Liquid Chromatography-APCI-Linear Ion Trap System

Supporting information

Matrix Factor Determination with the Waters Regulated Bioanalysis System Solution

A Fully Integrated Workflow for LC-MS/MS Analysis of Labeled and Native N-Linked Glycans Released From Proteins

Greazy: Open-Source Software for Automated Phospholipid MS/MS Identification. Michael Kochen

Supporting information

New Solvent Grade Targeted for Trace Analysis by UHPLC-MS

Non targeted Lipidomic Analysis by Direct Infusion Mass Spectrometry. Jianzhong Chen, PhD Assistant Professor School of Optometry UAB

Application of a new capillary HPLC- ICP-MS interface to the identification of selenium-containing proteins in selenized yeast

FOURIER TRANSFORM MASS SPECTROMETRY

2D-LC as an Automated Desalting Tool for MSD Analysis

Ion Source. Mass Analyzer. Detector. intensity. mass/charge

Identification & Confirmation of Structurally Related Degradation Products of Simvastatin

Supporting Information

Designer Fentanyls Drugs that kill and how to detect them. Cyclopropylfentanyl

Principles of Shotgun Lipidomics

Thermo Fisher Scientific, Sunnyvale, CA, USA; 2 Thermo Fisher Scientific, San Jose, CA, USA

Electronic Supplementary Information

One Gene, Many Proteins. Applications of Mass Spectrometry to Proteomics. Why Proteomics? Raghothama Chaerkady, Ph.D.

Ultra High Definition Optimizing all Analytical Dimensions

Impurity Identification using a Quadrupole - Time of Flight Mass Spectrometer QTOF

Sulfate Radical-Mediated Degradation of Sulfadiazine by CuFeO 2 Rhombohedral Crystal-Catalyzed Peroxymonosulfate: Synergistic Effects and Mechanisms

Comparison of Full Scan MS2 and MS3 Linear Ion Trap Approaches for Quantitation of Vitamin D

Using Software Tools to Improve the Detection of Impurities by LC/MS. Application Note. Christine Miller Agilent Technologies.

2. Ionization Sources 3. Mass Analyzers 4. Tandem Mass Spectrometry

Supplementary Table 1. Properties of lysates of E. coli strains expressing CcLpxI point mutants

Robust extraction, separation, and quantitation of structural isomer steroids from human plasma by SPE-UHPLC-MS/MS

The detergent-solubilized and gel filtration purified rhodopsin was partitioned against

Characterization and direct quantitation of cerebroside

Improved method for the quantification of lysophospholipids including enol ether

ABSTRACT. Catherine Fenselau, Professor, Department of Chemistry and Biochemistry

Structural Elucidation of N-glycans Originating From Ovarian Cancer Cells Using High-Vacuum MALDI Mass Spectrometry

Supplementary Figure 1. AdipoR1 silencing and overexpression controls. (a) Representative blots (upper and lower panels) showing the AdipoR1 protein

Rapid Analysis of Water-Soluble Vitamins in Infant Formula by Standard-Addition

The Raptor HILIC-Si Column

Polymer Additive Analysis by EI and APCI

Transcription:

SUPPLEMENTARY INFORMATION Phosphorylated glycosphingolipids essential for cholesterol mobilization in C. elegans Sebastian Boland, Ulrike Schmidt, Vyacheslav Zagoriy, Julio L. Sampaio, Raphael Fritsche, Regina Czerwonka, Tilo Lübken, Jakob Reimann, Sider Penkov, Hans-Joachim Knölker & Teymuras V. Kurzchalia 1

Supplementary Results Supplementary Figure 1 HPLC-MS separation of fraction 4 into more confined fractions, which were tested for their capability to abolish L2* arrest caused by sterol depletion. (a) Base-peak chromatogram of fraction 4 after column chromatography using rp-c18 LC-MS. The red labeled parts of the chromatogram represent the more confined fractions 6.1 to 6.4 and 10.1 to 10.4 which were (b) tested for their activity to rescue the L2* arrest. The results from experiments with biological duplicates in technical triplicates were pooled together and expressed as a percent value. Error bar, SD. 2

Supplementary Figure 2 High-resolution mass spectrometry analysis of the bioactive fraction 6. (a) Fourier transform MS (FTMS) analysis in a LTQ Orbitrap XL of the combined bioactive fraction 6 displays mmpegc-c22 in the protonated (m/z = 941.6769) and sodiated (m/z = 963.6587) forms. (b) Higher-energy collisional dissociation (HCD) MS2 analysis of the 941.7 precursor mass displays the fragments of the ceramide containing the C22-FA (m/z = 642.5997) and the polar head (m/z = 300.0832). (c) Ion trap MS3 (ITMS3) analysis of the 941.7 precursor mass followed by the polar head (300.1) fragment displays the mono-methyl phosphoethanolamine fragment. Water losses are marked with *. 3

Supplementary Figure 3 High-resolution mass spectrometry analysis of the bioactive fraction 10. (a) FTMS analysis in a LTQ Orbitrap XL of the combined bioactive fraction 10 displays mmpegc-c24 in the protonated (m/z = 969.7102) and sodiated (m/z = 991.6920) forms. (b) HCD MS2 analysis of the 969.7 precursor mass displays the fragments of the ceramide containing the C24-FA (m/z = 670.6321) and the polar head (m/z = 300.0832). (c) ITMS3 analysis of the 969.7 precursor mass followed by the polar head (300.1) fragment displays the monomethyl phosphoethanolamine fragment. Water losses are marked with *. 4

5

Supplementary Figure 4 Structural elucidation of the different PEGC species. FTMS2 experiments in positive ion mode of the precursors with HCD fragmentation: (a) m/z = 927.7, (b) m/z = 941.7, (c) m/z = 955.7, and (d) m/z = 969.7. Fragments corresponding to different ceramide backbones (642.6, 656.6, and 670.6) and their respective water losses (*). The inlets correspond to a zoom in on the low m/z where the polar head fragments are present. Two different polar heads, depending on the species, 300.1 (methylated head group) and 286.1 (nonmethylated head group) are present. (e-h) ITMS2 experiments in negative ion mode of the precursors with CID fragmentation: (e) m/z = 925.7, (f) m/z = 939.7, (g) m/z = 953.7, and (h) m/z = 967.7. In these spectra, the ceramide structure of the different species was resolved by measuring the intense fragments corresponding to the amide-linked α-hydroxylated fatty acids 355.4 (C22), 369.4 (C23), and 383.4 (C24). 6

7

Supplementary Figure 5 Comparison of isolated mmpegc-c22 and synthetic mmpegc- C22 (1) by LC-MS and MS2. (a,b) Extracted ion chromatograms of (a) isolated mmpegc-c22 and (b) synthetic mmpegc-c22 (1) displayed no difference in the retention time. (c,d) Comparison of the TOFMS and TOFMS2 spectra acquired on a Xevo G2-S revealed the same fragmentation pattern in the case of (c) the isolated mmpegc-c22 and (d) the synthetic mmpegc-c22 (1). (c,d) TOFMS2 data were acquired using a collision energy ramp from 20 ev to 50 ev. 8

Supplementary Figure 6 Expansion of an overlay of the COSY spectra of isolated and synthetic mmpegc-c22 (1). The COSY spectra (600 MHz, CD 3 OD) of isolated mmpegc-c22 in red and synthetic mmpegc-c22 (1) in green are superimposed. Overlapping cross peaks appear yellow. Due to the small amount of the isolated sample, some cross peaks could not be detected. 9

Supplementary Figure 7 Synthetic mmpegc-c22 (1) exhibits sterol-starvation rescue activity similar to the isolated mmpegc-c22. (a) The rescue capability of PEGC was investigated by the rescue ability of daf-12 mutant worms from sterol-starvation induced larval arrest (empty arrowheads). When either isolated mmpegcc22 or synthetic mmpegc-c22 (1) is fed to worms deprived of sterols the worms do not interrupt development but become fertile adults (filled arrowheads). The scale bars represent 0.5 mm. (b) Comparison of the activities of isolated mmpegc-c22 versus synthetic mmpegc-c22 (1) over a range of concentrations that were determined by LC-MS analysis. The results from experiments with biological duplicates in technical triplicates were pooled together and expressed as a percent value with concentrations ranging from 35 μm to 330 μm. The development of worms was scored after 4.5 d grown at 20 C. Error bar, SD. 10

11

Supplementary Figure 8 bre-3 but not cgt-3;cgt-1 extract is capable to reverse sterolstarvation induced larval arrest (L2*) due to different amounts of PEGC. (a) Simplified biosynthetic pathway of sphingolipids and complex glycolipids in C. elegans, including the catalytic enzymes (blue) and the corresponding genes (green). (b) Second generation of daf-12 mutants on sterol-free agarose plates arrest as L2* larvae (empty arrowheads) whereas daf-12 worms on 13 μm cholesterol develop to adults (filled arrowhead, offspring marked with asterisk). Feeding a cgt-3;cgt-1 extract/bacterial suspension does not rescue the L2* arrest (empty arrowheads) whereas a bre-3 extract/bacterial suspension leads to fertile adults (filled arrowheads, offspring marked with asterisk). Pictures were taken 4.5 d after bleaching and the scale bars represent 1 mm. (c) Quantification of PEGC content (the sum of individual PEGC species) in extracts derived from different genetic backgrounds (wild-type, bre-3, cgt-3;cgt-1 and ncr-2;ncr-1 mutant worms) by LC-MS. For quantification, two independent biological samples for each strains have been analyzed. Wild-type extract was regarded as the reference. 12

Supplementary Figure 9 PEGC does not facilitate worm development by dissolution of residual sterols from the medium. (a+b) Common detergents and substances similar to PEGC (e.g., d17iso-glccer (11) and sulfatides) were tested for their ability to rescue daf-12 worms from the sterol depletion-induced growth arrest. None of these substances promoted development to adulthood. (b) Quantification of the adult formation after 5 days. The experiments were performed in biological duplicates in technical triplicates pooled together and expressed as a percent value. Error bar, SD. 13

Supplementary Figure 10 Quantification of PEGC content in different generations. Histogram displays the sum of individual PEGC species in extracts derived from L2/L2* wild-type worms grown on sterol supplemented (P0) or on sterol-depleted conditions (F1 and F2). 14

Supplementary Figure 11 Full COSY spectrum of isolated mmpegc-c22. COSY spectra (600 MHz, CD 3 OD) of isolated mmpegc-c22. 15