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

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

Performance of an ultra low elution volume 96-well plate

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

Development of a High Sensitivity SPE-LC-MS/MS Assay for the Quantification of Glucagon in Human Plasma Using the ionkey/ms System

Reducing Sample Volume and Increasing Sensitivity for the Quantification of Human Insulin and 5 Analogs in Human Plasma Using ionkey/ms

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

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

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

Direct Analysis of Urinary Opioids and Metabolites by Mixed-Mode µelution SPE Combined with UPLC/MS/MS for Forensic Toxicology

LC-MS/MS for the quantification of Peptide biomarker and mixture of closely related Protein in formulation

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

Matrix Factor Determination with the Waters Regulated Bioanalysis System Solution

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

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

Reduced Ion Suppression and Improved LC/MS Sensitivity with Agilent Bond Elut Plexa

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

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

Rapid Analysis of Bisphenols A, B, and E in Baby Food and Infant Formula Using ACQUITY UPLC with the Xevo TQD

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

Latest Innovations in LC/MS/MS from Waters for Metabolism and Bioanalytical Applications

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

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

Paul D. Rainville Ph.D. Health Sciences Group Waters Corporation Waters Corporation 1

Quantification of Budesonide Using UPLC and Xevo TQ-S

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

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

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

Challenges in Developing an Ultra-Sensitive Bioanalytical Method for Ethinylestradiol in Human Plasma

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

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

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

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

Dienes Derivatization MaxSpec Kit

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

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

Author. Introduction. Small Molecule Pharmaceuticals & Generics

[ APPLICATION NOTE ] Oasis PRiME HLB Cartridge for Cleanup of Infant Formula Extracts Prior to UPLC-MS/MS Multiresidue Veterinary Drugs Analysis

Development and Validation of an UPLC-MS/MS Method for Quantification of Mycotoxins in Tobacco and Smokeless Tobacco Products

[ APPLICATION NOTE ] A Generic Kit-Based Approach for LC-MS/MS Quantification of Urinary Albumin for Clinical Research APPLICATION BENEFITS

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

Noora Perkola Finnish Environment Institute. Nordic MS Symposium November 9, 2011, Båstad, Sweden

Vitamin D Metabolite Analysis in Biological Samples Using Agilent Captiva EMR Lipid

Rapid Lipid Profiling of Serum by Reverse Phase UPLC-Tandem Quadrupole MS

Comparison of Biotage Extrahera vs. Manual Sample Processing Using a Vacuum Manifold

[ APPLICATION NOTE ] High Sensitivity Intact Monoclonal Antibody (mab) HRMS Quantification APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS KEYWORDS

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

Rapid, Simple Impurity Characterization with the Xevo TQ Mass Spectrometer

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

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

Determination of β2-agonists in Pork Using Agilent SampliQ SCX Solid-Phase Extraction Cartridges and Liquid Chromatography-Tandem Mass Spectrometry

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

Determination of Amantadine Residues in Chicken by LCMS-8040

Analysis of drugs of abuse in biological matrix using Time of Flight technology

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

Detection of Cotinine and 3- hydroxycotine in Smokers Urine

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

Application Note. Author. Abstract. Introduction. Food Safety

Supporting Information

The setup and validation of an LC-MS/MS assay of Androstenedione & Testosterone a labs experience

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

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

LC-MS/MS analysis of Chlorates in Milk and Whey Powder using the Agilent 6470 QQQ

SEPARATION OF BRANCHED PFOS ISOMERS BY UPLC WITH MS/MS DETECTION

Quantitative LC-MS/MS Analysis of Glucagon. Veniamin Lapko, Ph.D June 21, 2011

Detection, Confirmation, and Quantification of Chloramphenicol in Honey, Shrimp and Chicken Using the Agilent 6410 LC/MS Triple Quadrupole

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

Using Hydrophilic Interaction Chromatography (HILIC) for the Retention of Highly Polar Analytes

A NOVEL METHOD OF M/Z DRIFT CORRECTION FOR OA-TOF MASS SPECTROMETERS BASED ON CONSTRUCTION OF LIBRARIES OF MATRIX COMPONENTS.

Finnur Freyr Eiríksson

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

PosterREPRINT SIMULTANEOUS QUANTIFICATION OF PSYCHOTHERAPEUTIC DRUGS IN HUMAN PLASMA BY TANDEM MASS SPECTROMETRY

Analysis of Pesticides (II) Metribuzin & their metabolites in Rice Jun Yonekubo, Nihon Waters, JAPAN

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

LC-MS/MS Method for the Determination of 21 Opiates and Opiate Derivatives in Urine

Fast quantitative Forensic Analysis of THC and its Metabolites in Biological Samples using Captiva EMR- Lipid and LC/MSMS

High resolution mass spectrometry for bioanalysis at Janssen. Current experiences and future perspectives

Comprehensive Forensic Toxicology Screening in Serum using On-Line SPE LC-MS/MS

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

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

Simplifying Solid-Phase Extraction [ OASIS SOLID-PHASE EXTRACTION PRODUCTS ]

Michael Blackburn HOW LOW CAN YOU GO: DRIVING DOWN LIMITS OF HYBRID IA-LC/MS. European Bioanalytical Forum. 19 th November 2015

Extraction of Synthetic and Naturally Occurring Cannabinoids in Urine Using SPE and LC-MS/MS

MS/MS as an LC Detector for the Screening of Drugs and Their Metabolites in Race Horse Urine

High Throughput Extraction of Opiates from Urine and Analysis by GC/MS or LC/MS/MS)

Development and Validation of a Polysorbate 20 Assay in a Therapeutic Antibody Formulation by RP-HPLC and Charged Aerosol Detector (CAD)

The Development of LC/MS Methods for Determination of Polar Drugs of Abuse in Biological Samples

Comparison of a UPLC Method across Multiple UHPLC Systems

Author. Introduction. Abstract

Abstract. Introduction

Analysis of Food Sugars in Various Matrices Using UPLC with Refractive Index (RI) Detection

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

Amphetamines, Phentermine, and Designer Stimulant Quantitation Using an Agilent 6430 LC/MS/MS

Validation Report 8. EURL for Cereals and Feeding stuff National Food Institute Technical University of Denmark

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

The Raptor HILIC-Si Column

[ APPLICATION NOTE ] APPLICATION BENEFITS INTRODUCTION WATERS SOLUTIONS KEYWORDS

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

Development and Validation of Multiresidue Pesticide Methods at FDA/CFSAN

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

Transcription:

Development of an SPE-LC/MS/MS Assay for the Simultaneous Quantification of Amyloid Beta Peptides in Cerebrospinal Fluid in Support of Alzheimer s Research Dr. Erin E. Chambers Waters Corporation Presented by Dr. Diego Rodriguez Cabaleiro Waters Europe 211 Waters Corporation 1

Background: Amyloid β Peptides Clinical significance of amyloid β peptides Formation of aggregates/plaques in the brain is a critical event in Alzheimer s Disease Drug development strategies aimed at lowering production of these peptides or enhancing their clearance o Inhibition/modulation of beta and gamma secretase enzyme Current analytical methodologies ELISA- based assays Immunoprecipitation (IP) followed by LCMSMS 211 Waters Corporation 2

Amyloid β Peptides for Quantification in CSF Amyloid β 1-38 DAEFRHDSGYEVHHQKLVFFAEDVGSNKGAIIGLMVGG MW 4132, pi 5.2, HPLC index 96 Amyloid β 1-4 DAEFRHDSGYEVHHQKLVFFAEDVGSNKGAIIGLMVGGVV MW 433, pi 5.2, HPLC index 13 Amyloid β 1-42 DAEFRHDSGYEVHHQKLVFFAEDVGSNKGAIIGLMVGGVVIA MW 4516, pi 5.2, HPLC index 117 Internal standards are N15 labeled versions of 1-38, 1-4, and 1-42 211 Waters Corporation 3

Waters Regulated Bioanalysis System Solution Sample Preparation Solutions Best in class ACQUITY UPLC I-Class The fastest and most resolving LC without compromise in robustness ACQUITY UPLC Columns Different choices for best performance TQ-S Most sensitive MS UNIFI Compliant, Interactive workflow-driven data platform Service Installation, maintenance & training Compliance services 211 Waters Corporation 4

Outline Introduction Mass Spectrometry Liquid Chromatography Choice of Standard Curve Matrix Solid Phase Extraction Partial Validation 211 Waters Corporation 5

Why LCMSMS? Why an LCMSMS based assay? ELISA assays not practical for discovery, no antibodies available yet Challenges with ELISA assays o time consuming, expensive to develop o require separate assay for each peptide o limited linear dynamic range o Possible cross reactivity Benefits of LC/MS/MS for peptides LCMSMS provides single assay for multiple amyloid peptides Broad linear dynamic range Accurate, precise Universal Faster, cheaper method development 211 Waters Corporation 6

Specific Challenges in Developing an LCMSMS Assay for Amyloid β Peptides Extremely hydrophobic Very poor peptide solubility High level of aggregation High level of non-specific binding (NSB) Low MS sensitivity Very large and hydrophobic Form many low abundance fragments Specificity in matrix 211 Waters Corporation 7

ESI- MSMS Spectra for Amyloid β 1-42 1 1126.76 M-4H 4- Daughters of 1127ES- 1.55e5 -H 2 O 1122.33 1117.78 Non-specific water loss 5 55 6 65 7 75 8 85 9 95 1 15 11 115 12 125 13 135 14 145 m/z 211 Waters Corporation 8

ESI+ MSMS Spectra for Amyloid β 1-42 1 b39 153.3 b4 178.52 Daughters of 1129ES+ 1.62e4 M+H 4+ b38 b41 116.86 b32 b34 1256.5 b33 b35 914.52 942.73 975.36 128.67 b36 12.8 b35 b38 b39 b4 1371.29 13.38 144.12 1437.73 b34 1.65 5 55 6 65 7 75 8 85 9 95 1 15 11 115 12 125 13 135 14 145 m/z 4+ fragments 3+ fragments 211 Waters Corporation 9

Amyloid β Peptide 1-42: Identification of Fragments with BioLynx In Silico Fragmentation Model Fragment choice is 4+ b 4 ion 211 Waters Corporation 1

Positive Ion versus Negative Ion Detection: Specificity 1-42 in Human CSF 25pgmL_hCSF_3291_2x 2.1 2: MRM of 3 Channels ES- 91.2 > 897.6 (a Beta 1-42) 7.5e4 2.12 Amyloid β 1-42 ESI- 6.4 1.12 2.7 5.54 2.21 5.66 3.88 4.6 4.27 4.39 4.89 5.5 5.95 25pgmL_hCSF_3291_2x 1: MRM of 3 Channels ES+ 6.39 1129 > 178.5 (a Beta 1-42) 1.2e4 Amyloid β 1-42 6.58 6.62 7.7 ESI+ 1 1.21 3.82 6.6 6.2 6.43 7.18 6.92 6.5 7.19 Time 211 Waters Corporation 11

Positive Ion versus Negative Ion Detection: Specificity 1-38 in Human Plasma Amyloid β 1-38 6.45 2: MRM of 3 Channels ES- 825 > 821.3 (a Beta 1-38) 3.35e5 5.2 7.3 ESI- 2.12 5.93 6.7 4.61 4.91 5.11 5.23 5.69 6.69 1: MRM of 3 Channels ES+ 5.93 133.5 > 1.3 (a beta 1-38) 2.99e4 Amyloid β 1-38 5.94 ESI+ 5.99 6.67 4.96 6. 5.1 5.81 4.83 6.65 2.18 4.22 4.6 5.41 7.17 6.95 7.28 7.57 7.39 7.94 Time 211 Waters Corporation 12

Effect of Using Higher m/z Precursor/Fragment: plasma 4- Precursor/fragment 2.48 MRM of 2 Channels ESa Beta 1-38 3.2e4 3.36.5 1. 1.5 2. 2.5 3. 3.5 MRM of 2 Channels ES- 2.48 a Beta 1-38 3.26e4 5- Precursor/fragment 1.22 1.63 1.67 1.96 2.49.5 1. 1.5 2. 2.5 3. 3.5 Time 211 Waters Corporation 13

Xevo TQ-S MSMS Conditions Xevo TQ-S MS operated in ESI+ mode MRM Transitions: Peptide Name Precursor Ion 4+ Product Ion 4+ Product Ion ID Cone voltage (V) Collision energy (ev) Amyloid β 1-38 133.5 1.3 b 36 33 23 Amyloid β 1-38 N15 IS 146 112.5 3 22 Amyloid β 1-4 183 153.6 b 39 33 25 Amyloid β 1-4 N15 IS 196 166.5 35 22 Amyloid β 1-42 1129 178.5 b 4 28 3 Amyloid β 1-42 N15 IS 1142.5 191.5 35 28 211 Waters Corporation 14

Impact of MS Platform Change Solvent Standard Comparison: Area counts for 5 pg/ml standard Xevo TQ Xevo TQ-S amyloid β 1-38 18 1468 amyloid β 1-4 133 1741 amyloid β 1-42 54 1589 211 Waters Corporation 15

Xevo TQ-S LOD: 12.5 pg/ml solvent standard in 5/5 elution solvent/water 12pt5pgmL_abetas_7261_1 Sm (SG, 3x5) 1 5.81 125. MRM of 3 Channels ES+ 1129.5 > 178.9 (Amyloid Beta 1-42) 5.58e3 Area Amyloid β 1-42 Peak Area 125 3. 3.5 4. 4.5 5. 5.5 6. 6.5 7. 7.5 12pt5pgmL_abetas_7261_1 Sm (SG, 3x5) MRM of 3 Channels ES+ 1 183.3 > 154 (Amyloid Beta 1-4) 5.58e3 Area 5.62 98. Amyloid β 1-4 Peak Area 98 3. 3.5 4. 4.5 5. 5.5 6. 6.5 7. 7.5 12pt5pgmL_abetas_7261_1 Sm (SG, 3x5) MRM of 3 Channels ES+ 1 5.39;129.9 133.75 > 1.75 (Amyloid Beta 1-38) 5.58e3 Area Amyloid β 1-38 Peak Area 13 3. 3.5 4. 4.5 5. 5.5 6. 6.5 7. 7.5 Time 1µL injection 211 Waters Corporation 18

Outline Introduction Mass Spectrometry Liquid Chromatography Choice of Standard Curve Matrix Solid Phase Extraction Partial Validation 211 Waters Corporation 19

UPLC Conditions: Final Method Column: 2.1 X 15mm, ACQUITY BEH C18 3Å, 1.7μm Mobile phase A:.3 NH 4 OH by volume, or.1 absolute Mobile Phase B: 9/1 ACN/mobile phase A Temperature: 5 C SNW: 65/25/1 ACN/water/NH 4 OH SNW volume: 6 µl WNW: 9/1 water/acn +.3 NH 4 OH WNW volume: 6 µl Flow rate:.2 ml/min Injection mode: partial loop Injection Volume: 1 µl Injection Solvent for standards: SPE elution solvent diluted with water; SPE elution solvent = 75 ACN, 15 water, 1 NH 4 OH Gradient Table 211 Waters Corporation 2

Representative Chromatogram: Extracted Spiked Artificial CSF Amyloid β 1-4 5.85 4.6e4 5.6 Amyloid β 1-42 Amyloid β 1-38 6.3 6.87 7.65 4.89 5.3 6.31 7.97 2 Time 211 Waters Corporation 21

Representative Chromatography: Extracted Human CSF Sample Basal Levels in Human CSF hcsf_pool1_basal_421_1 1-42 N15 IS 6.2 6.1 6.6 MRM of 6 Channels ES+ 1142.5 > 191.5 (a Beta 1-42 N15) 2.77e4 6.53 6.76 7.47 7.69 hcsf_pool1_basal_421_1 MRM of 6 Channels ES+ 6.3 1129 > 178.5 (a Beta 1-42) 6.1 6.5 8.54e3 1.25 1.85 5.88 6.47 4.9 5.42 6.61 7.77.18 7.67 6.18 7.817.91 1 hcsf_pool1_basal_421_1 MRM of 6 Channels ES+ 5.85 196 > 166.5 (a Beta 1-4 N15) 5.87 6.29e4 5.89 4.8 6.37 6.58 hcsf_pool1_basal_421_1 MRM of 6 Channels ES+ 5.85 183 > 153.6 (a Beta 1-4) 1-4 1.16e5 5.88 5.52 hcsf_pool1_basal_421_1 MRM of 6 Channels ES+ 5.61 146 > 112.5 (a Beta 1-38 N15) 5.62 4.5e4 5.67 5.36 6.46 6.67 7.7 hcsf_pool1_basal_421_1 MRM of 6 Channels ES+ 5.61 133.5 > 1.3 (a beta 1-38) 2.31e4 5.63 1.19 1-42 1-4 N15 IS 1-38 N15 IS 1-38 211 Waters Corporation 22 5.27 5.67 5.9 6.39 6.75 7.2 7.98 Time

Outline Introduction Mass Spectrometry Liquid Chromatography Choice of Standard Curve Matrix Solid Phase Extraction Partial Validation 211 Waters Corporation 23

Average Basal Levels in Human CSF: Comparison of Results with Different Standard Curve Preparations Standard curves prepared from either artificial CSF or by over-spiking human CSF Conc.(ng/mL) Source 1 Conc. (ng/ml) Source 2 Amyloid β 1-38 Conc from curve in art CSF.82.826 Conc from curve in human CSF.679 n/a Conc.(ng/mL) Source 1 Conc. (ng/ml) Source 2 Amyloid β 1-4 Conc from curve in art CSF 3.713 3.136 Conc from curve in human CSF 4.335 n/a average.75 std deviation.1 RSD 13.32 average 4.24 std deviation.44 RSD 1.93 Conc.(ng/mL) Source 1 Conc. (ng/ml) Source 2 Amyloid β 1-42 Conc from curve in art CSF 1.15.763 Conc from curve in human CSF 1.189.84 average 1.147.784 std deviation.59.29 RSD 5.178 3.7 *Human CSF corrected for basal level 211 Waters Corporation 24

Outline Introduction Mass Spectrometry Liquid Chromatography Choice of Standard Curve Matrix Solid Phase Extraction Partial Validation 211 Waters Corporation 25

Sample Extraction: Pretreatment Sample Pretreatment Spike human or artificial CSF + 5 rat plasma samples, mix Equilibrate samples at room temperature for 3 minutes Remove 5 µl spiked artificial CSF (to which 5 rat plasma was added) for standard curves, or human/monkey CSF (basal level or over-spike QC s) Add 5µL 5M guanidine HCl Shake samples at room temperature for 45 minutes Add 5µL 4 H 3 PO 4 in water, mix Note: 4X less sample is used than TQ MS method: 5 µl instead of 2 µl 211 Waters Corporation 26

Sample Extraction: Final Method Oasis MCX μelution Plate Condition: 2 µl MeOH Equilibrate: 2 µl 4 H 3 PO 4 Amyloid β Peptide SPE Recovery 1-38 94 1-4 92 1-42 9 Load: 15 μl diluted sample (pretreated sample: 5 µl human CSF, 5µL 5M guanidine HCl, 5µL 4 H 3 PO 4 in water) Wash 1: 2 µl 4 H 3 PO 4 Wash 2: 2 µl 1 ACN in water (by volume) Elute: 2 X 25 µl 75/1/15 ACN/conc. NH 4 OH/water (by volume) Dilute: 25 µl water Inject: 1 µl 211 Waters Corporation 27

Key Attributes for High Extraction Recovery Wash with no more than 1 ACN Removes polar interferences Does not impact recovery of 1-38 (earliest eluting/least hydrophobic of these 3 amyloid β peptides) Elute with no less than 75 ACN Provides required elutropic strength for 1-4 and 1-42 (the more hydrophobic of these 3 peptides) Elute with no less than 1 NH 4 OH Provides required solubility to fully elute 1-42 (least soluble/most hydrophobic of these 3 peptides) Addition of rat plasma to artificial CSF to eliminate nonspecific binding increases SPE recovery in this matrix from 6 on average to >9 Guanidine HCl denaturation Improves reproducibility of method; eliminates aggregation and protein binding 211 Waters Corporation 28

Impact of MS Platform: Standard Curve and QC Range Comparison 2 µl sample 5 µl sample Xevo TQ Xevo TQ-S Standard Curve Range.1 to 1 ng/ml.25 or.5 to 1 ng/ml QC Range.2 to 6 ng/ml.4 to 6 ng/ml 211 Waters Corporation 3

Outline Introduction Mass Spectrometry Liquid Chromatography Choice of Standard Curve Matrix Solid Phase Extraction Partial Validation 211 Waters Corporation 31

Summary of Samples Extracted Standard curves prepared in artificial CSF + 5 Rat plasma Calibration points are.25,.5,.1,.25,.35,.5,.75, 1, 5, 7.5, and 1 ng/ml Basal levels in human CSF 3 individual sources pooled human CSF samples, 1 source cynomalgous monkey 6 replicates from each source QC samples Prepared in each of the human CSF matrices 7 concentrations:.4,.75,.15,.2,.8, 2 and 6 ng/ml over-spike N=3 for each concentration, from each source of CSF 211 Waters Corporation 32

Representative Chromatogram: Basal Levels of Amyloid β 1-38 in Human and Monkey CSF hcsf_pool1_basal_421_1 Basal Level Amyloid β 1-38 5.61 MRM of 6 Channels ES+ 133.5 > 1.3 (a beta 1-38) 2.31e4 Human CSF, pooled sample 1 5.27 1.19 6.75 5.79 5.9 6.39 7.2 7.98 hcsf_pool2_basal_421_1 MRM of 6 Channels ES+ 5.61 133.5 > 1.3 (a beta 1-38) 5.6 2.96e4 Human CSF, pooled sample 2 5.63 5.64 5.66 1.12 2.12 5.26 5.91 6.23 6.546.74 7.13 hcsf_pool3_basal_421_1 MRM of 6 Channels ES+ 5.61 133.5 > 1.3 (a beta 1-38) 1.33e4 Human CSF, pooled sample 3 6.5 6.74 2.12 3.99 5.94 1.22 6.21 6.96 7.62 7.86 1 cyno_csf_pool_basal_421_1 MRM of 6 Channels ES+ 5.62 133.5 > 1.3 (a beta 1-38) 2.43e4 Monkey CSF, pooled sample 1 5.6 5.59 5.65 2.12 5.4 5.23 5.74 6.18 1.11.29 6.36 6.79 6.96 7.71 7.82 Time 211 Waters Corporation 33

Representative Chromatogram: Basal Levels of Amyloid β 1-4 in Human and Monkey CSF Basal Level Amyloid β 1-4 hcsf_pool1_basal_421_1 Human CSF, pooled sample 1 5.85 5.88 MRM of 6 Channels ES+ 183 > 153.6 (a Beta 1-4) 1.16e5 5.52 hcsf_pool2_basal_421_1 MRM of 6 Channels ES+ 5.85 183 > 153.6 (a Beta 1-4) 1.47e5 Human CSF, pooled sample 2 hcsf_pool3_basal_421_1 MRM of 6 Channels ES+ 5.86 183 > 153.6 (a Beta 1-4) 8.91e4 Human CSF, pooled sample 3 cyno_csf_pool_basal_421_1 MRM of 6 Channels ES+ 5.86 183 > 153.6 (a Beta 1-4) 1.37e5 Monkey CSF, pooled sample 1 6.57 Time 211 Waters Corporation 34

Representative Chromatogram: Basal Levels of Amyloid β 1-42 in Human and Monkey CSF Basal Level Amyloid β 1-42 hcsf_pool1_basal_421_1 Human CSF, pooled sample 1 6.3 MRM of 6 Channels ES+ 1129 > 178.5 (a Beta 1-42) 6.61e3 1.25 1.85 5.93 5.42 5.71 6.47 7.18 6.59 7.717.817.91 hcsf_pool2_basal_421_1 MRM of 6 Channels ES+ 6.4 1129 > 178.5 (a Beta 1-42) 8.77e3 Human CSF, pooled sample 2 1 1.85 3.91 4.98 hcsf_pool3_basal_421_1 MRM of 6 Channels ES+ 6.4 1129 > 178.5 (a Beta 1-42) 4.87e3 Human CSF, pooled sample 3 5.74 5.91 6.3 6.41 6.64 7.88 6.87 2 99 1.1 1.22 1.89 5.16 5.9 6.1 6.42 6.74 6.92 7.48 cyno_csf_pool_basal_421_1 MRM of 6 Channels ES+ 1.86 6.4 1129 > 178.5 (a Beta 1-42) 8.13e3 Monkey CSF, pooled sample 1 7.93-1 1.16 2.9 4.76 4.91 5.94 6.36 6.47 7.86 6.88 7.5 7.24 Time 211 Waters Corporation 35

Baseline Levels of Amyloid β in Pooled Human and Monkey CSF Amyloid Beta 1-38 Human CSF Pool 1 ng/ml Human CSF Pool 3 ng/ml Human CSF Replicate # Pool 2 ng/ml 1 1.585 2.354 1.14 1.713 2 1.65 2.13 1.371 1.65 3 1.614 2.464.95 1.947 4 1.657 1.939 1.68 1.541 5 1.82 2.158 1.471 1.675 6 1.486 1.995 1.167 1.644 Mean 1.635 2.169 1.264 1.688 Std. Deviation.11.24.262.14 CV 6.7 9.4 2.7 8.3 Cyno CSF Pool 1 ng/ml Amyloid Beta 1-42 Human CSF Pool 1 ng/ml Human CSF Pool 3 ng/ml Human CSF Replicate # Pool 2 ng/ml 1.519.616.421.675 2.421.656.481.621 3.542.644.534.623 4.471.567.348.659 5.476.573.487.7 6.561.713.51.688 Mean.498.628.463.661 Std. Deviation.52.55.68.33 CV 1.4 8.7 14.7 5.1 Cyno CSF Pool 1 ng/ml Amyloid Beta 1-4 Human CSF Pool 1 ng/ml Human CSF Pool 3 ng/ml Human CSF Replicate # Pool 2 ng/ml 1 3.83 4.31 2.541 3.699 2 3.391 3.776 2.593 3.989 3 3.292 3.598 2.58 3.525 4 2.884 3.533 2.612 3.956 5 3.131 3.23 2.58 3.284 6 3.656 3.619 2.49 3.595 Mean 3.24 3.631 2.554 3.675 Std. Deviation.269.266.49.268 CV 8.3 7.3 1.9 7.3 Cyno CSF Pool 1 ng/ml 211 Waters Corporation 36

Response Residual Representative Standard Curve: Amyloid β 1-42 Compound name: Amyloid Beta 1-42 Correlation coefficient: r =.998799, r^2 =.9976 Calibration curve:.887923 * x +.13161 Response type: Internal Std ( Ref 2 ), Area * ( IS Conc. / IS Area ) Curve type: Linear, Origin: Exclude, Weighting: 1/x, Axis trans: None 1.. -1. Conc 5.. Conc. 2. 4. 6. 8. 1. 211 Waters Corporation 37

Representative Standard Curve: Amyloid β 1-42 Name Type Std. Conc RT Area IS Area Response Conc. Dev blank artificial CSF 5.73 19.7 7. 5 pg/ml artificial CSF Standard.5 5.71 23.4 362.5.64.57 14 1 pg/ml artificial CSF Standard.1 5.71 39.8 3585.1.19.18 8.1 25 pg/ml artificial CSF Standard.25 5.71 778.3 3737.3.28.22-12 35 pg/ml artificial CSF Standard.35 5.71 1267.3 3693.8.343.372 6.2 5 pg/ml artificial CSF Standard.5 5.71 1494.7 3566.8.419.457-8.5 75 pg/ml artificial CSF Standard.75 5.71 2733.5 4152..658.727-3.1 1 ng/ml artificial CSF Standard 1 5.71 3166.8 3792.5.835.926-7.4 5 ng/ml artificial CSF Standard 5 5.72 14773.9 3148.3 4.693 5.27 5.4 7.5 ng/ml artificial CSF Standard 7.5 5.72 24576.9 3877. 6.339 7.125-5 1 ng/ml artificial CSF Standard 1 5.72 33343.3 3662.5 9.14 1.238 2.4 211 Waters Corporation 38

Average Deviation Values for all Overspike QC Samples QC.4 ng/ml QC.75 ng/ml QC.15 ng/ml QC.2 ng/ml QC.8ng/mL QC 2 ng/ml QC 6 ng/ml Amyloid β 1-38 Human CSF 1 and 2 2.3 5.8-3.2 7.3 14.8 5.1 13.1 Amyloid β 1-4 Human CSF 1 and 2 -.8-3.2-1.9 2.5-2.6-4.2-3.8 Amyloid β 1-42 Human CSF 1 and 2 1.3 13.4-3.6 5.6 2. -.6 -.2 211 Waters Corporation 4

Conclusions Single flexible LC/MS/MS platform developed for simultaneous quantification of multiple amyloid peptides Highly selective sample preparation based on mixed-mode SPE Improved MS selectivity using positive ion mode and sequence ion fragments High sensitivity using new MS platform Highly reproducible, accurate, and precise Sample pretreatment and choice of SPE and LC solutions eliminate handling (NSB, losses, etc.) problems One method for multiple Aβ peptides, advantage over ELISA which requires individual assays for each peptide Fast, simple sample prep 211 Waters Corporation 42

Total Solution for Regulated Bioanalysis - Bioanalysis of Peptides Sample Prep Kits and protocols µelution plate No evaporation & reconstitution 15x concentration UNIFI IntelliStart and BioLynx functionalities Multiple charge precursor ions ACQUITY UPLC I Class & Columns Lower dispersion Dedicated PST columns Longer columns if needed Lowest carryover Xevo TQ-S Stepwave Mass range Minimal dwell time RADAR PIC SERVICE Application support and troubleshooting 211 Waters Corporation 43

Acknowledgements Mary E. Lame, Neuroscience Research Unit, Pfizer Global R&D 211 Waters Corporation 44