NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Influences of blood sample processing on low-molecular-weight proteome identified by surface-enhanced laser desorption/ionization mass spectrometry.

Author(s): Banks R E, Stanley A J, Cairns D A, Berrett J H, Clarke P, Thompson D, Selby P J

Publication: Clin Chem, 2005, Vol. 51, Page 1637

PubMed ID: 16002455 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to assess the impacts of anticoagulants, time until separation (0 to 24 h), and collection tube type on the spectral profiles of proteins isolated from plasma and serum samples.

Conclusion of Paper

The protein spectral profiles of plasma were altered in an anticoagulant- and time delay- dependent manner (as soon as 4 h), with citrate yielding the least amount of variation over time. While robust changes in peak intensity were observed in serum over short periods of time (30 min), changes attributable to tube type were minimal. The authors recommend a minimal clotting time of 30 to 60 min prior to serum analysis when using tubes that promote rapid clotting.

Studies

  1. Study Purpose

    The purpose of this study was to determine if the type of anticoagulant or the duration of time before centrifugation (0 -24 h at room temperature) impacts the protein spectral profile of plasma specimens.

    Summary of Findings:

    Compared to time zero controls, plasma samples demonstrated differential peaks in an anticoagulant dependent manner after a 4 hour delay at room temperature before processing; plasma specimens containing EDTA, heparin, and citrate displayed variation in 5-10%, 1-6%, and 0-3% of peaks, respectively, depending upon the chip used for analysis. A delay of 24 hours yielded even more robust changes, with 29% of peaks exhibiting either increased or decreased intensity compared to time zero controls.

    Biospecimens
    Preservative Types
    • Frozen
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Protein SELDI-TOF MS
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Time at room temperature 30 min
    1 h
    2 h
    4 h
    24 h
    0 h
    Biospecimen Acquisition Anticoagulant EDTA
    Citrate
    Heparin
    None
    SELDI-TOF MS Specific Technology platform CM10 chip
    IMAC30-Cu chip
    H50 chip
    Biospecimen Aliquots and Components Centrifugation Centrifugation delays investigated
  2. Study Purpose

    The purpose of this study was to determine if the type of collection tube or the duration of clotting time (0 to 24 h at room temperature) impacts the protein spectral profile of serum specimens.

    Summary of Findings:

    Compared to time zero controls, the spectral profile of serum samples collected in activator tubes showed significant changes in 12-36% of peaks after 4 hours dependent upon the chip used for analysis. However, many of these changes were increases in peak intensity and were present as soon as 30 minutes after venipuncture. Tube-dependent effects were limited to 2 peaks displaying a higher intensity in gel tubes, and 2 peaks displaying a lower intensity compared to activator tubes after 30 minutes at room temperature.

    Biospecimens
    Preservative Types
    • Frozen
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Protein SELDI-TOF MS
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Acquisition Type of collection container/solution Greiner vacuette activator
    Plain tube
    Gel serum separator
    Storage Time at room temperature 0 min
    30 min
    1 h
    2 h
    4 h
    Biospecimen Aliquots and Components Centrifugation Centrifugation delays investigated

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