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Prothymosin alpha in human blood.

C Panneerselvam, A A Haritos, J Caldarella

    Proceedings of the National Academy of Sciences of the United States of America
    |July 1, 1987
    PubMed
    Summary
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    The primary peptide cross-reacting with thymosin alpha 1 assays in human blood is prothymosin alpha, mainly found in leukocytes. This study quantifies prothymosin alpha levels in blood, revealing its significant presence beyond thymosin alpha 1.

    Area of Science:

    • Immunology
    • Biochemistry
    • Molecular Biology

    Background:

    • Thymosin alpha 1 is a key immunomodulatory peptide.
    • Radioimmunoassays (RIAs) are used to detect thymosin alpha 1.
    • Cross-reactivity in assays can lead to misidentification of related peptides.

    Purpose of the Study:

    • To identify the major cross-reacting peptide in human plasma detected by thymosin alpha 1 RIA.
    • To quantify the levels of this peptide in human blood components.
    • To determine the accurate concentration of prothymosin alpha in circulation.

    Main Methods:

    • Gel-filtration chromatography for peptide separation.
    • High-performance liquid chromatography (HPLC) for purification.
    • Radioimmunoassay (RIA) for peptide detection and quantification.

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  • Amino acid composition analysis.
  • Main Results:

    • Prothymosin alpha was identified as the major cross-reacting peptide in human plasma and leukocytes.
    • Less than 10% of cross-reacting material consisted of lower molecular weight thymosin alpha 1-like peptides.
    • Total cross-reacting material in blood was 11-14 pmol/ml (thymosin alpha 1 equivalents), with 90% in leukocytes.
    • Estimated prothymosin alpha content in human blood is 55-70 pmol/ml (0.6-0.8 microgram/ml) after accounting for RIA reactivity.

    Conclusions:

    • Prothymosin alpha is the predominant thymosin alpha 1-like peptide in human blood.
    • Leukocytes are the main source of prothymosin alpha in circulation.
    • Accurate quantification of prothymosin alpha requires correction for RIA cross-reactivity.