1 / 29

Proteored Multicentric Experiment 8 (PME8)

Proteored Multicentric Experiment 8 (PME8) Quantitative Targeted Analysis in Proteomics. An Assesment Study (QTAPAS). ProteoRed WG1-WG2 Meeting Pamplona, December 10th 2013. Total 27 Participant Laboratories ( February - April 2013). 20 SRM data sets. 10 PRM data sets:.

sugar
Télécharger la présentation

Proteored Multicentric Experiment 8 (PME8)

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. ProteoredMulticentric Experiment 8 (PME8) QuantitativeTargetedAnalysis in Proteomics. AnAssesmentStudy (QTAPAS) ProteoRed WG1-WG2 Meeting Pamplona, December 10th 2013

  2. Total 27 ParticipantLaboratories (February- April 2013) 20 SRM data sets 10 PRM data sets: 3 QTOF 7 OT

  3. SIGMA-ALDRICH MSQC1 • 6 Digestedproteins : • 25-fold concentrationrange – 3 concentrationtiers • Quantified UV beforedigestion • 2-3 labeledpeptides/ protein • L/H ratios 0.2-50 • Quantified AAA

  4. SAMPLE SET YeastDigest + Spiked MSQC1, 5 differentconcentrations fmol/ microgramYeastLysateDigest

  5. LABELED PEPTIDES

  6. QTAPAS - PME8 SRM ANALYSIS RECOMMENDED GUIDELINES • 1- LC conditions: • Nano LC- system: • Column: 75 mm x 15 cm C18 • Sample load: 1 mg yeast digest/injection • Flow rate: 300-500 nL /min • Gradient: 0-35% Acetonitrile in 90 min 3- Analysis design: - Samples A through E Replica 1 (from most diluted to most concentrated) - Blank runs (enough to secure clean baseline) - Samples A through E Replica 2 - Blank runs - Samples A through E Replica 3

  7. http://www.proteored.org/PME8_main.asp

  8. LINEARITY OF RESPONSE Average of 30 datasets – Error bars: StdDev. Tier 1

  9. Tier 2

  10. Tier 3

  11. ABSOLUTE QUANTIFICATION INTER LABORATORY VARIABILITY %CV 30 datasets Average of 30 datasets , three replicas averaged

  12. ABSOLUTE QUANTIFICATION INTER LABORATORY VARIABILITY N=20 N=7

  13. ABSOLUTE QUANTIFICATION INTER LABORATORY VARIABILITY N=20 N=3

  14. fmolmeasured

  15. %CV

  16. ABSOLUTE QUANTIFICATION Comparisonbytype of measurement

  17. ABSOLUTE QUANTIFICATION INTRA- vs INTER LABORATORY VARIABILITY Average, %CV 3 replicas - Average, %CV 30 datasets

  18. INTRA- vs INTER LABORATORY VARIABILITY Average, %CV 3 replicas - Average, %CV 30 datasets

  19. REPRODUCIBILITY OF TRANSITION PATTERN Transitionsignaldistribution Average 3 replicas Normalizeddotproducttoaveragedistribution

  20. REPRODUCIBILITY OF TRANSITION PATTERN

  21. INTRA- vs INTER LABORATORY VARIABILITY

  22. Analysis of pure MSQC1 (withoutyeastbackground) Forcomparison: Possibleeffects of complexbackground 3 Vials x 10 mg 200 nginjection – 80 fmol min

  23. EUPA 2013

  24. CONCLUSIONS • The results demonstrate a good degree of reproducibility of targeted quantification measurements by SRM at different laboratories, irrespective of the method of analysis and the spectrometer used. • The average Inter-Laboratory %CV of the measured absolute protein amounts ranges from less than 10%CV for Tier 1 proteins, to 40-60% for the proteins at the lowest concentrations. • The pattern of relative intensities of the transitions monitored is fairly consistent among different instruments and fragmentation modes, underscoring the utility of spectral databases for the design of quantification methods. • The results obtained at each laboratory allow the assessment of the limitations in sensitivity and limits of quantification under the diverse analytical conditions used

More Related