Material Measurement Laboratory Mass Spectral Database of Glycans and Glycopeptides in Therapeutic Drugs Maria Lorna A. De Leoz, Xinjian (Eric) Yan, Xiaoyu.

Slides:



Advertisements
Similar presentations
Improvements in Mass Spectrometry for Life Science Research – Does Agilent Have the Answer? Ashley Sage PhD.
Advertisements

De novo glycan structure search with CID MS/MS spectra of native N-glycopeptides Hannu Peltoniemi
Conclusion The workflow presented provides a strategy to incorporate unbiased glycopeptide identification to generate an initial list of targets for data.
Mass Spectrometry Mass spectrometry involves ionizing a compound, separating the ions that result on the basis of mass to charge ratio (m/z) and obtaining.
Analysis of human haptoglobin, digest with trypsin and Glu-C – six putative N-motif peptides. Glycopeptide separation by hydrophilic interaction liquid.
Orbitrap Mass Analyzer
ACCELERATING CLINICAL AND TRANSLATIONAL RESEARCH Metabolomics/Proteomics and Genomics at IUB Indiana CTSI – Purdue Retreat Monday,
N-Glycopeptide Identification from CID Tandem Mass Spectra using Glycan Databases and False Discovery Rate Estimation Kevin B. Chandler, Petr Pompach,
How to identify peptides October 2013 Gustavo de Souza IMM, OUS.
PROTEIN IDENTIFICATION BY MASS SPECTROMETRY. OBJECTIVES To become familiar with matrix assisted laser desorption ionization-time of flight mass spectrometry.
ProReP - Protein Results Parser v3.0©
Computational Methods for Biomarker Discovery in Proteomics and Glycomics Vijetha Vemulapalli School of Informatics Indiana University Capstone Advisor:
Proteomics Informatics Workshop Part I: Protein Identification
Previous Lecture: Regression and Correlation
Proteomics Informatics – Overview of Mass spectrometry (Week 2) Ion Source Mass Analyzer Detector mass/charge intensity.
Proteomics Josh Leung Biology 1220 April 13 th, 2010.
Proteomics Informatics (BMSC-GA 4437) Course Director David Fenyö Contact information
Proteomics Informatics – Overview of Mass spectrometry (Week 2)
Evaluated Reference MS/MS Spectra Libraries Current and Future NIST Programs.
Tryptic digestion Proteomics Workflow for Gel-based and LC-coupled Mass Spectrometry Protein or peptide pre-fractionation is a prerequisite for the reduction.
Karl Clauser Proteomics and Biomarker Discovery Taming Errors for Peptides with Post-Translational Modifications Bioinformatics for MS Interest Group ASMS.
Mass Spectrometry Mass spectrometry involves ionizing a compound, separating the ions that result on the basis of mass to charge ratio (m/z) and obtaining.
Analysis of human haptoglobin, after digest with trypsin and Glu-C – six putative N-linked motif peptides. Glycopeptide separation by hydrophilic interaction.
MS/MS Libraries of Identified Peptides and Recurring Spectra in Protein Digests Lisa Kilpatrick, Jeri Roth, Paul Rudnick, Xiaoyu Yang, Steve Stein Mass.
Acknowledgements This work is supported by NSF award DBI , and National Center for Glycomics and Glycoproteomics, funded by NIH/NCRR grant 5P41RR
Additional file 1 1.1Workflow of large-scale proteomic analysis of normal human kidney glomerulus 1.2Detailed procedure of LC-MS/MS analysis Additional.
Laxman Yetukuri T : Modeling of Proteomics Data
ETD & ETD/PTR Electron Transfer Dissociation Proton Transfer Reaction
Glycopeptide Analysis (LC-MS) Marker Screening by T-Test, MFC, and ROC Protein and Sugar Chain Identification Glyco Feature Analysis Serum Glycoproteins.
Clustering of MS/MS spectra for glycan biomarker discovery Anoop Mayampurath, Chuan-Yih Yu.
Finnish Custom Lab., Pekka Ravio
Multiple flavors of mass analyzers Single MS (peptide fingerprinting): Identifies m/z of peptide only Peptide id’d by comparison to database, of predicted.
PRINCIPLE, APPLICATIONS & ADVANCES IN
Separates charged atoms or molecules according to their mass-to-charge ratio Mass Spectrometry Frequently.
Proteomics Informatics (BMSC-GA 4437) Instructor David Fenyö Contact information
Salamanca, March 16th 2010 Participants: Laboratori de Proteomica-HUVH Servicio de Proteómica-CNB-CSIC Participants: Laboratori de Proteomica-HUVH Servicio.
Metabolomics MS and Data Analysis PCB 5530 Tom Niehaus Fall 2015.
Supplementary Data Average Monosaccharide Composition Calculations Example data in this table originates from work done for the following publication:
Material Measurement Lab Material Measurement Laboratory Mass Spectrometry Data Center Biomolecular Measurement Division Q. Dong; M. Lorna A. De Leoz;
2014 생화학 실험 (1) 6주차 실험조교 : 류 지 연 Yonsei Proteome Research Center 산학협동관 421호
Material Measurement Lab Material Measurement Laboratory Q. Dong; M. Lorna A. De Leoz; L.E. Kilpatrick; Y. Liang; X. Yan; X. Yang; S.E. Stein Building.
Constructing high resolution consensus spectra for a peptide library
Introduction to Liquid Phase Mass Spectrometry
Yonsei Proteome Research Center Peptide Mass Finger-Printing Part II. MALDI-TOF 2013 생화학 실험 (1) 6 주차 자료 임종선 조교 내선 6625.
Target Analyses in Parallel Reaction Monitoring Mode (PRM)
MS Libraries for Forensics: DART-MS and GC-MS
Goals in Proteomics Identify and quantify proteins in complex mixtures/complexes Identify global protein-protein interactions Define protein localizations.
Proteomics Informatics – Overview of Mass spectrometry (Week 2)
Minimum Information Required for A Glycomics Experiment
National High Magnetic Field Laboratory- ICR Group
S2 Fig. Ion suppression for aniline, 4-aminopyridine and 4-aminobenzontrile Left: ESI-MS response in presence of 1 mM different, pH-modifying electrolytes.
Mass Spectrometry Mass spectrometry involves ionizing a compound, separating the ions that result on the basis of mass to charge ratio (m/z) and obtaining.
Authors: Aruna Jyothi. M, Sanovar Bhargava, Hima Bindu. A, Subbarayudu
Thomas BOTZANOWSKI & Blandine CHAZARIN
Bioinformatics Solutions Inc.
Minimum Information Required for A Glycomics Experiment
Proteomic Approaches to Cancer Biomarkers
Nat. Rev. Rheumatol. doi: /nrrheum
The Haystack Is Full of Needles: Technology Rescues Sugars!
A, high resolution MS/MS spectrum (lower panel) of 1435
Diagnostics and Prognostics
Beam-type (Q-TOF) CID data of m/z (3+).
Relative quantitation of phosphopeptides from conditioned media from subtype specific breast cancer cell lines. Relative quantitation of phosphopeptides.
Time course of phosphorylation changes at Ser-293, Ser-300, and Ser-232 in PDHE1α following kinase inhibition with DCA. A, relative quantitation over three.
MS/MS spectra of INEILSNALKR with a Lys residue modified with SUMO1 or SUMO3 remnant chains. MS/MS spectra of INEILSNALKR with a Lys residue modified with.
Resolution and mass accuracy of A, a peptide isotope cluster (m/z 558
Mass Spectrometry THE MAIN USE OF MS IN ORG CHEM IS:
Top-down analysis of intact bovine carbonic anhydrase II by LTQ Orbitrap Velos. Top-down analysis of intact bovine carbonic anhydrase II by LTQ Orbitrap.
Tryptic glycopeptides of IGFBP-5 from T47D cells separated by HPLC detected by ESI-MS and sequenced by tandem MS.a, ESI-MS spectrum of combined fractions.
Monitoring the acetylation profile of mitochondrial proteins in SIRT3 KO mice. Monitoring the acetylation profile of mitochondrial proteins in SIRT3 KO.
Presentation transcript:

Material Measurement Laboratory Mass Spectral Database of Glycans and Glycopeptides in Therapeutic Drugs Maria Lorna A. De Leoz, Xinjian (Eric) Yan, Xiaoyu (Sara) Yang, Lisa Kilpatrick, Yuxue Liang, Michael Tarlov, Stephen Stein

Therapeutic Monoclonal Antibodies are Widely Used in Medicine Used as treatment for cancer and several other diseases $20B market/year >30 approved mAbs 6/10 best-selling drugs, mAbs – monoclonal antibodies

Therapeutic Monoclonal Antibodies Are Glycosylated Glycans are attached to the protein molecules Changes in glycosylation may affect drug safety and efficacy Glycosylation highly heterogeneous Glycan analysis remains a formidable challenge Adapted from Oxford Glycobiology Institute Glycans Fab Fc Monoclonal Antibody Therapeutic Protein 3

Protein denaturation Glycoprotein N-glycan release Decantate Precipitate Ethanol precipitation Solid phase extraction Liquid chromatography Mass spectrometry N-GLYCANS ARE RELEASED FROM PROTEINS De Leoz, M.L.A.; Young, L.J.T.; An, H.J.; Kronewitter, S.; et al., Mol Cell Proteomics 2011; 10, M

N-GLYCANS ARE ANALYZED BY MASS SPECTROMETRY Can analyze using ion trap or orbitrap MS Sample injected through LC or direct infusion Several MS/MS activation methods Higher-energy C-trap Dissociation (HCD) Collisionally-Induced Dissociation (CID by ion trap or orbitrap) Electron Transfer Dissociation (ETD) High mass resolution Max at 125,000 at m/z 400 (i.e. it can distinguish peaks at m/z and ) High mass accuracy < 5 ppm error routinely ESI-LTQ Velos/Orbitrap MS 5

* * * * * * * * 10% ACN (+) 20% ACN (+) 40% ACN (-) Relative Intensity Hexose (Hex) N-acetylhexosamine (HexNAc)  Fucose (Fuc)  Sialic Acid (NeuAc) De Leoz, M.L.A.; Young, L.J.T.; An, H.J.; Kronewitter, S.; et al., Mol Cell Proteomics 2011; 10, M N-Glycan Profiling of Serum Glycoproteins

STARTER GLYCAN MS/MS LIBRARY NGA4 2 G0 NGA2F 1 G0F NGA3B 1,2 G0B NA2G1F 1 G1F A1F 1 G2FS NA2F 1 G2F A2F 1 G2FS2 NGA2B 2 G0B NGA2 1 G0 NGA4B 2 G0B 1 Purchased; 2 Kindly provided by the Consortium for Functional Glycomics through Dr. Jim Paulson

Glycan Consensus Spectrum Y4,Y4Y4,Y4 B4B4 [M+Na] + Y3,Y3Y3,Y3 Y 4 /Y 4  B 3, B 4 /Y 4 , B 4 /Y 4 0,2 A 5 0,2 A 4 0,2 A 4 /Y 4 0,2 A 4 /Y 4  B 4 /Y 3  B 4 /Y 3 B 3 /Y 4 , B 3 /Y 4 B 3 /Y 3 , B 3 /Y 3 -H 2 O 2,4 A 5 [M+2Na] 2+ -(2H 2 O+CH 2 O) B4B4 Y4Y4 Y4Y4 Y3Y3 Y3Y3 B3B3 Mannose N-acetylglucosamine [M+2Na] 2+ HCD, 55eV

Glycopeptide Consensus Spectrum b2 y2y4b5 b6 [M+2H] 2+ -(2H 2 O+CH 2 O) (TKPREEQYNSTYR)= p y1 0,2 A 1 oxonium p-NH 3 -H 2 O p-NH 3 -NH 3 2,4 A 1 m/z , z=3 HCD, 62eV p p p p p p p p p

Glycan from Rituximab Matches Library Rituximab Glycan Library Head to Tail Comparison