Exploring Changes in Primary Metabolites in Alzheimer s Disease using Targeted LC-MS/MS

Similar documents
Integration of steroids analysis in serum using LC-MS/MS with full-automated sample preparation

Fully Automated Online Sample Preparation AND Quantification of Amiodarone from Whole Blood using CLAM-LC-MS/MS

High Throughput simultaneous analysis of 39 amino acids in various foods without derivatization using LC-MS/MS

Fully automated sensitive determination of immunosuppressant drugs in whole blood, using high quality internal standardization

Summary Chapter 8 CHAPTER 8. Summary. Page 173

Vitamin D3 and related compounds by ESI and APCI

Determination of Amantadine Residues in Chicken by LCMS-8040

Liquid Chromatograph Mass Spectrometer LCMS-8040 C146-E188E

All stocks and calibration levels were prepared in water: methanol (50:50) v/v to cover range of all steroid concentrations (refer Table 1).

LCMS-8030 Application Report. Steroids: Testosterone, Progesterone, Estradiol, Ethinylestradiol

Separation and Quantitation of Oxysterol Compounds Using LC-MS/MS. Liquid Chromatography Mass Spectrometry SSI-LCMS-082

Supporting Information (SI)

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

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

A Novel Solution for Vitamin K₁ and K₂ Analysis in Human Plasma by LC-MS/MS

LC/MS Analysis of Various Hydrophilic Compounds Using a Polymer-Based Amino Column - Shodex TM HILICpak TM VG-50 2D

A Robustness Study for the Agilent 6470 LC-MS/MS Mass Spectrometer

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

LC/MS Method for Comprehensive Analysis of Plasma Lipids

Determination of Unbound Urinary Amino Acids Incorporated with Creatinine Normalization by LC-MS/MS Method with CLAM-2000 Online Sample Pre-treatment

Extraction of Aflatoxin M1 From Infant Formula Using ISOLUTE Myco SPE Columns prior to LC-MS/MS Analysis

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

Removal of Triton X-100 from Plasma Samples Using Mixed-Mode Solid Phase Extraction (SPE)

Phospholipid characterization by a TQ-MS data based identification scheme

A UPLC/MS Approach for the Diagnosis of Inborn Errors of Metabolism

Profiling of Endogenous Metabolites Using Time-of-Flight LC/MS with Ion Pair Reverse Phase Chromatography

Highly sensitive simultaneous quantitative analysis of estrone and equilin from plasma using LC/MS/MS

Comprehensive Two-Dimensional HPLC and Informative Data Processing for Pharmaceuticals and Lipids

The Raptor HILIC-Si Column

[ APPLICATION NOTE ] UPLC-MS/MS Analysis of 45 Amino Acids Using the Kairos Amino Acid Kit for Biomedical Research INTRODUCTION APPLICATION BENEFITS

Maria João Mendes Mendonça Barreira Department of Health Promotion and Chronic Deseases, INSA

Quantitative analysis of hydrophilic metabolite using ion-paring chromatography with a high-speed triple quadrupole mass spectrometer

Designer Cannabinoids

DETERMINATION OF CANNABINOIDS, THC AND THC-COOH, IN ORAL FLUID USING AN AGILENT 6490 TRIPLE QUADRUPOLE LC/MS

Profiling and Quantitation of Metabolomic Signatures for Breast Cancer Cell Progression

Application Note LCMS-108 Quantitation of benzodiazepines and Z-drugs in serum with the EVOQ TM LC triple quadrupole mass spectrometer

4.5 Minute Analysis of Benzodiazepines in Urine and Whole Blood Using LC/MS/MS and an Ultra Biphenyl Column

LC/MS/MS Analysis of Metabolites of Synthetic Cannabinoids JWH-018 and JWH-073 in Urine

SPE-LC-MS/MS Method for the Determination of Nicotine, Cotinine, and Trans-3-hydroxycotinine in Urine

Comparison of FIA and on-column LC-MS/MS method to measure simultaneously ABG, ASM, GAA, GALC, GLA and IDUA activities

Simple Cancer Screening Based on Urinary Metabolite Analysis

Analysis of Testosterone, Androstenedione, and Dehydroepiandrosterone Sulfate in Serum for Clinical Research

Unique Retention and Selectivity of Pentafluorophenylpropyl Phases for High-Throughput LC/MS Analysis

John Haselden 1, Gordon Dear 1, Jennifer H. Granger 2, and Robert S. Plumb 2. 1GlaxoSmithKline, Ware, UK; 2 Waters Corporation, Milford, MA, USA

A RAPID AND SENSITIVE ANALYSIS METHOD OF SUDAN RED I, II, III & IV IN TOMATO SAUCE USING ULTRA PERFORMANCE LC MS/MS

Simultaneous Analysis of Active Pharmaceutical Ingredients and Their Counter-Ions Using a Mixed-Mode Column

Fast and simultaneous analysis of ethanol metabolites and barbiturates using the QTRAP 4500 LC-MS/MS system

Extraction of Multiple Mycotoxins From Nuts Using ISOLUTE Myco prior to LC-MS/MS Analysis

A Novel Platform of On-line Sample Pre-treatment and LC/MS/MS Analysis for Screening and Quantitation of Illicit Drugs in Urine

Extraction of 25-hydroxy Vitamin D from Serum Using ISOLUTE. PLD+ Prior to LC-MS/MS Analysis

Providing a Universal, One-step Alternative to Liquid-Liquid Extraction in Bioanalysis

Extraction of Multiple Mycotoxins From Grain Using ISOLUTE Myco prior to LC-MS/MS Analysis

Rapid and Accurate LC-MS/MS Analysis of Nicotine and Related Compounds in Urine Using Raptor Biphenyl LC Columns and MS-Friendly Mobile Phases

Supplementary Information. Effects of Perfluorooctanoic Acid on Metabolic Profiles in Brain and Liver of Mouse by a

Raptor HILIC-Si: Simplify the Switch to HILIC

Profiling Analysis of Polysulfide Silane Coupling Agent

Liquid Chromatograph Mass Spectrometer LCMS-8050 C146-E232A

Jose Castro-Perez, Henry Shion, Kate Yu, John Shockcor, Emma Marsden-Edwards, Jeff Goshawk Waters Corporation, Milford, MA, U.S. and Manchester, UK

Abstract. Introduction

Quantitation of Protein Phosphorylation Using Multiple Reaction Monitoring

Analysis of anti-epileptic drugs in human serum using an Agilent Ultivo LC/TQ

Quantification of lovastatin in human plasma by LC/ESI/MS/MS using the Agilent 6410 Triple Quadrupole LC/MS system

UPLC-MS/MS Analysis of Azole Antifungals in Serum for Clinical Research

Low-level environmental phthalate exposure associates with urine metabolome. alteration in a Chinese male cohort

[ APPLICATION NOTE ] APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS KEYWORDS

LC-MS/MS Method for the Determination of Tenofovir from Plasma

A Simple and Accurate Method for the Rapid Quantitation of Drugs of Abuse in Urine Using Liquid Chromatography

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

Core E Analysis of Neutral Lipids from Human Plasma June 4, 2010 Thomas J. Leiker and Robert M. Barkley

High-Resolution Analysis of Intact Triglycerides by Reversed Phase HPLC Using the Agilent 1290 Infinity LC UHPLC System

Metabolomic fingerprinting of serum samples by direct infusion mass spectrometry

Uptake and Metabolism of Phthalate Esters by Edible Plants

A High Sensitivity UPLC/MS/MS Method for the Analysis of Clopidogrel and Clopidogrel Carboxylic Acid Metabolite in Human K 2 EDTA Plasma

Author. Introduction. Abstract

A Definitive Lipidomics Workflow for Human Plasma Utilizing Off-line Enrichment and Class Specific Separation of Phospholipids

Neonatal Screening using Shimadzu LCMS-8040

Analysis of Rosuvastatin in Dried Blood Spot and Plasma Using ACQUITY UPLC with 2D Technology

Simultaneous Analysis of Intact Human Insulin and Five Analogs in Human Plasma Using μelution SPE and a CORTECS UPLC Column

PHOTOCATALYTIC DECONTAMINATION OF CHLORANTRANILIPROLE RESIDUES IN WATER USING ZnO NANOPARTICLES. DR. A. RAMESH, Ph.D, D.Sc.,

Edgar Naegele. Abstract

Extraction of a Comprehensive Steroid Panel from Human Serum Using ISOLUTE. SLE+ Prior to LC/MS-MS Analysis

Breaking the Sensitivity Barrier in Triple Quad LC/MS Performance

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

Choosing the metabolomics platform

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

Method Development for the Analysis of Endogenous Steroids Using Convergence Chromatography with Mass Spectrometric Detection

Ultra High Performance Liquid Chromatograph. Nexera X2 C196-E079

Metabolomics Core Lab School of Medicine University of Utah

Analytes. Sample Preparation Procedure. Introduction. Format: Sample Pre-treatment. Sample Loading. Analyte Extraction and Derivatization.

Oxysterol, Secosterols, and Cholesterol Intermediates Separation and Quantitation Using Triple Quadrupole Mass Spectrometry

Meeting Challenging Requirements for the Quantitation of Regulated Growth Promoters Dexamethasone and Betamethasone in Liver and Milk

Supporting Information

Automated Targeted screening of Benzodiazepines in urine using LDTD-MS/MS at 400 samples per hour rate

Overview. Introduction. Experimental. Cliquid Software for Routine LC/MS/MS Analysis

LCMS Vitamin D3 Method development

UPLC/MS Monitoring of Water-Soluble Vitamin Bs in Cell Culture Media in Minutes

LC/MS/MS of Trichothecenes and Zearalenone in Wheat Using Different Sample Prep Methods

LC-MS Analysis of Amino Acids on a Novel Mixed-Mode HPLC Column

Fig. 1: Chemical structure of arachidonic acid COOH CH 3

Transcription:

PO-CON1694E Exploring Changes in Primary Metabolites in Alzheimer s Disease using Targeted LC-MS/MS MSACL 216 EU Nicola Gray 1, Stuart Snowden 2, Min Kim 2, Chris Titman 1, Cristina Legido-Quigley 2 1 Shimadzu UK, Milton Keynes, UK 2 King s College London, UK

Introduction High-throughput and unbiased global profiling metabolomic approaches provide a suitable platform to analyse variations in metabolite levels, offering insights into mechanisms of disease through the discovery of novel biomarkers. Targeted approaches, however, offer a more specific, sensitive and quantitative measure for selected compounds. Here we investigate biochemical changes in enzymatic and metabolic processes at the cellular level in patients with Alzheimer s Disease (AD) using a LC-MS/MS for primary metabolites in plasma. A method using a pentafluorophenylproyl (PFPP) column enables the comprehensive analysis of 97 hydrophilic and hydrophobic primary metabolites. Using this approach the simultaneous analysis of amino acids, organic acids, nucleotides, nucleosides and co-enzymes was performed on 33 plasma samples from AD patients and 43 age- and sex-matched controls. Methods Human plasma (2 µl) was prepared using a two-phase extraction with methyl tert-butyl ether (MTBE) and methanol/water. The methanol/water phase was injected directly into the LC-MS/MS. Data were processed using LabSolutions and Traverse TM MS Multivariate Analysis Software for MRM Data (Shimadzu Corporation, Japan), SIMCA P 14. (Umetrics, Sweden) and R packages for further statistical analysis. Liquid chromatography LC system : Shimadzu Nexera X2 Column : Discovery HS F5-3 (15 x 2.1 mm, 3 µm) Mobile phase A :.1 % formic acid in water Mobile phase B :.1 % formic acid in acetonitrile Flow rate :.25 ml/min Column temperature : 4 C Injection volume :.5 µl Binary gradient : Time (mins) %B Time (mins) %B. 15. 95 2. 2. 95 5. 25 2.1 11. 35 25. Mass spectrometry MS system : Shimadzu LCMS-86 Ionisation : Heated ESI (positive/negative) Dwell time : 5 msec Pause time : 1 msec Polarity switching : 5 msec Source temperatures : Interface: 35 C Heat block: 3 C Desolvation line: 15 C Gas flows : Heated gas (air): 1 L/min Drying gas (N2): 1 L/min Nebulising gas (N2): 3 L/min 2

Results and discussion Figure 1 shows a representative MRM chromatogram of the from a pooled quality control (QC) of all healthy controls and AD patient samples considered in this study. Peak area measurements for 62 metabolites were detected with CV < 3% across QC samples, used to determine the level of metabolic change between control and AD patients. A number of these metabolites exhibited significant changes between control and AD samples by applying a t-test, with a summary of the most significant findings shown in Figure 2. Figure 1 Chromatogram of 62 metabolites detected in human plasma extract and overlaid metabolites exhibiting significant change between control and AD samples. 3

Figure 2 Pareto scaled plots for metabolites with most significant change between control and AD samples. Of particular interest were the changes in the expression of neurotransmitters. As an example, the box plots in Figure 3 show the variation in metabolic changes in the serotonin synthesis pathway. From these results, we can see the decrease of tryptophan and serotonin in the AD plasma (Figure 3A and B), which complement similar findings from measurements made in a separate study of brain tissue (Figure 3C and D). Figure 3 Box plots highlighting changes in tryptophan and serotonin levels between control and disease groups in plasma (A and B) and in brain tissue (C and D). Brain tissue analysis as part of a separate study; data not shown here. 4

A reduction in tryptophan, coupled with an increase in the abundance of the aromatic amino acid decarboxylase (AAAD) inhibitor alpha-synuclein in the brain of AD patients, suggests a mechanism for the reduction of serotonin in the brain. The reduction in the abundance of this monoamine neurotransmitter would result in impaired signal transmission in the brain of AD patients, leading to cognitive function decline (Figure 4). Figure 4 Illustration of serotonin synaptic transmission with normal (A) and reduced (B) serotonin levels 5

Conclusions In this presentation we have shown the comprehensive analysis of primary metabolites in human plasma, which revealed metabolic changes between control and AD patients This targeted approach focused on primary metabolites provides a sensitive and selective way of exploring biochemical changes leading to AD Variation in a number of metabolites suggest perturbations in purine metabolism, the urea/tca cycle and serotonin metabolism in AD Reduced plasma tryptophan and serotonin suggest a disturbance in neurotransmission, changes to which may result in reduced signal transduction in AD patients Acetylcholinesterase inhibitors are well established treatments for AD, and the results of this study suggest the need to consider the abundance of other neurotransmitters. First Edition: October, 216