new proteomics strategies for studying alzheimer's and ... · pino et al, anal chem, 2018....
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New Proteomics Strategies for Studying Alzheimer's and
Related DementiasMacCoss, Hoofnagle, and Montine Labs
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Projects Related to Signatures of AD and Related Dementias
• Neuropathological assessment of resilience in post-mortem braino Can we have a molecular assay that can distinguish between:
Different AD genetic risk Associated co-morbities Resilience to AD neuropathologic change
o Can we develop a proteomics assay to use as a replacement of traditional histopathological assessment.
• Cerebral spinal fluid assay that can reflect brain pathophysiologyo Can we expand beyond the use of CSF Aβ42, tau, and P181-tau, and PET imaging for
amyloid and pathologic tau protein
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
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Mass Spectrometry Data Acquisition Strategies Used in Proteomics
Data Dependent Acquisition (DDA)
Peptide Identification
NLPFSVENK
Database Searching
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10Peptide 11Peptide 12Peptide 13Peptide 14Peptide 15Peptide 16Peptide 17Peptide 18Peptide 19Peptide 20Peptide 21Peptide 22Peptide 23Peptide 24Peptide 25Peptide 26Peptide 27Peptide 28Peptide 29Peptide 30
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Mass Spectrometry Data Acquisition Strategies Used in Proteomics
Data Dependent Acquisition (DDA)
Peptide Identification
NLPFSVENK
Database Searching
Parallel Reaction Monitoring (PRM)
Peptide Quantification
NLPFSVENK
Targeted Analysis
Cycle time
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10Peptide 11Peptide 12Peptide 13Peptide 14Peptide 15Peptide 16Peptide 17Peptide 18Peptide 19Peptide 20Peptide 21Peptide 22Peptide 23Peptide 24Peptide 25Peptide 26Peptide 27Peptide 28Peptide 29Peptide 30
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10
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Mass Spectrometry Data Acquisition Strategies Used in Proteomics
Data Dependent Acquisition (DDA)
Peptide Identification
NLPFSVENK
Database Searching
Parallel Reaction Monitoring (PRM)
Peptide Quantification
NLPFSVENK
Targeted Analysis
Cycle time
Data Independent Acquisition (DIA)
NLPFSVENK NLPFSVENK
Cycle time
~50 Hz• 4 m/z isolation (2 m/z
effective)• 500-900 m/z • 2 s Cycle Time
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10Peptide 11Peptide 12Peptide 13Peptide 14Peptide 15Peptide 16Peptide 17Peptide 18Peptide 19Peptide 20Peptide 21Peptide 22Peptide 23Peptide 24Peptide 25Peptide 26Peptide 27Peptide 28Peptide 29Peptide 30
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10
Condition 1 Condition 2 Condition 3 Condition 4Peptide 1Peptide 2Peptide 3Peptide 4Peptide 5Peptide 6Peptide 7Peptide 8Peptide 9Peptide 10Peptide 11Peptide 12Peptide 13Peptide 14Peptide 15Peptide 16Peptide 17Peptide 18Peptide 19Peptide 20Peptide 21Peptide 22Peptide 23Peptide 24Peptide 25Peptide 26Peptide 27Peptide 28Peptide 29Peptide 30
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Improving Precursor Selectivity
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Improving Precursor Selectivity
Amodei et al JASMS 2019
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20 m/z DIA
GVMNAVNNVNNVIAAAFVK
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20 m/z DIA + Overlap
GVMNAVNNVNNVIAAAFVK
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20 m/z DIA + Overlap + Demultiplexing
GVMNAVNNVNNVIAAAFVK
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10 m/z DIA
GVMNAVNNVNNVIAAAFVK
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Separating Detection from Quantitation
24 m/z overlapping12 m/z effective
4 m/z overlapping2 m/z effective
Searle et al, Nature Comm, 2018
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
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Are the Measurements Quantitative or Differential?
Can we define LOQ and LOD for many peptides at once?
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Assessment of LOD and LOQ
Building on:Galitzine C et al, MCP 2018
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Matched Matrix Dilution Curves
Building on:Grant and Hoofnagle, Clin Chem 2014
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Not all Peptides are Equal Quantitative Proxies for a Protein
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Not all Peptides are Quantitative
• Detectable Peptides• Quantitative Peptides
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
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Comparing Signal Intensities Between Labs, Instrument PlatformsSignal Calibration in Proteomics?
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Peak area measurements should scale with the amount of peptide in the sample
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known quantity
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Measurements on different platforms are not measured on the same scale
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Between Batch/Platform/Lab Signal Calibration
Purpose of signal calibration
• Placing signal on the same scale
• Often the scale is arbitraryo Kilogram = mass of a liter of water at freezing pointo Meter = 1/10,000,000 the distance from the equator to the
north poleo Pee dee belomnite (PDB) = reference for 13C, fossil found in
Peedee Formation in South Carolinao Standard mean ocean water (SMOW) = reference for 18O,
arbitrary mix of distilled water from different regions of the world.
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Data harmonization between days, instrument platforms, and laboratories
experimental
reference(control)
(osmotic shock)
yeast
BY4741Ghaemmaghami et alNature 2003
Pino et al, Anal Chem, 2018
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Aliquots of reference material are prepared together with each experimental batch
Reference material aliquots
Experimental samples
Pino et al, Anal Chem, 2018
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Data harmonization between days, instrument platforms, and laboratories
between daysbetween instrument platforms
between laboratories
Pino et al, Anal Chem, 2018
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Signals measured on different platforms are often on different scales
between instrument platforms
Pino et al, Anal Chem, 2018
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External reference calibration places different platforms on the same scale
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between instrument platforms
Pino et al, Anal Chem, 2018
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Calibration to the same reference minimizes quantitative variance
Pino et al, Anal Chem, 2018
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Calibration to the same reference minimizes quantitative variance
Pino et al, Anal Chem, 2018
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Calibration to the same reference minimizes quantitative variance
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Calibration to the same reference minimizes quantitative variance
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Pino et al, Anal Chem, 2018
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
![Page 36: New Proteomics Strategies for Studying Alzheimer's and ... · Pino et al, Anal Chem, 2018. Aliquots of reference material are prepared together with each experimental batch. Reference](https://reader033.vdocument.in/reader033/viewer/2022042916/5f57721de1ce3f4de814acc8/html5/thumbnails/36.jpg)
Different Peptides Reflect Different ProteoformsAmyloid Precursor Protein
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Different Peptides Reflect Different Proteoforms7
Tau
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So what do we need?
• We need methods that sample the same peptides in all samples
• We need methods where the change in signal reflects the change in quantity
• We need methods where we can get the same signal despite differences in sample preparation, instrument platform, etc…
• We need to recognize that changes can occur with individual peptides and not the overall gene product.
• We need a large sample size.
![Page 39: New Proteomics Strategies for Studying Alzheimer's and ... · Pino et al, Anal Chem, 2018. Aliquots of reference material are prepared together with each experimental batch. Reference](https://reader033.vdocument.in/reader033/viewer/2022042916/5f57721de1ce3f4de814acc8/html5/thumbnails/39.jpg)
Shift from a Triangular Process to a Rectangular
Number of Samples
Discovery
Number of Samples
Validation
Discovery
Validation
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Shift from a Triangular Process to a Rectangular
Number of Samples
Discovery
Number of Samples
Validation
Discovery
Validation
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Measuring More Analytes Requires Measuring More Samples
Lazzeroni and Ray Mol Psychiatry. 2012 Jan; 17(1): 108–114.
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Conclusions• Data independent acquisition offers systematic sampling over
traditional discovery proteomics.
• We have the ability to perform DIA with selectivity of 50% the precursor isolation window size across the entire m/z range.
• Dynamic range and sensitivity that approximates PRM but is comprehensive
• Signal can be calibrated between labs and instrument platforms using a common external reference sample
• Stop doing protein roll up for bottom-up proteomics.
• Proteomics assays that measure lots of peptides require lots of samples.
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Financial SupportNIGMS BTRR P41 ProgramNIH Common Fund – LINCS ProgramNIA Nathan Shock CenterNIA Investigator Initiated R01 and P01NIGMS Investigator Initiated R01sIARPA Program
University of WashingtonDepartment of Genome SciencesBill NobleJohn StamatoyannopolousJudit Villen and Lab
The Broad InstituteJake Jaffe and Lab
UW Lab MedicineAndy Hoofnagle
NortheasternOlga Vitek and Lab
Former Lab MembersJarrett EgertsonBrian SearleSandi SpencerSonia Ting
University of WashingtonMacCoss LabJosh AldrichNat BraceBrian ConnollyDanielle FaivreAlex FederationAustin KellerEric HuangRich JohnsonBrendan MacLeanGennifer MerrihewBrook NunnLindsay PinoDeanna PlubellBrian PrattPaul RudnickVagisha SharmaNick ShulmanEmma Timmins-Schiffman
Stanford Tom Montine
ThermoFisherMary BlackburnRomain HuguetAndreas KuehnPhil RemesMike SenkoYue XuanVlad Zabrouskov
Acknowledgement
Software Vendor SupportAgilent ShimadzuBruker ThermoFisherSciex Waters
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MacCoss Lab UW