The nascent polypeptide-associated complex is required for intracellular translocation of newly synthesized polypeptides in eukaryotic cells. It may also act as a transcriptional coactivator in humans and various eukaryotic organisms and binds to nucleic acids. Recently, we provided evidence that a component of nascent polypeptide-associated complex, alpha-nascent polypeptide-associated complex, represents an IgE-reactive autoantigen for atopic dermatitis patients. By oligonucleotide screening we isolated a complete cDNA coding for a so far unknown alpha-nascent polypeptide-associated complex isoform from a human epithelial cDNA library. Southern blot hybridization experiments provided further evidence that alpha-nascent polypeptide-associated complex is encoded by a gene family. Recombinant alpha-nascent polypeptide-associated complex was expressed in Escherichia coli as a soluble, His-tagged protein, and purified via nickel affinity chromatography. By circular dichroism analysis it is demonstrated that purified recombinant alpha-nascent polypeptide-associated complex represents a folded protein of mixed alpha-helical and beta-sheet conformation with unusual high thermal stability and remarkable refolding capacity. Complete recombinant alpha-nascent polypeptide-associated complex (215 amino acids) and its 86 amino acid C-terminal fragment specifically bound IgE autoantibodies. Recombinant alpha-nascent polypeptide-associated complex also inhibited IgE binding to natural alpha-nascent polypeptide-associated complex, demonstrating the presence of common IgE epitopes between the recombinant and natural protein. Furthermore, recombinant alpha-nascent polypeptide-associated complex induced specific lymphoproliferative responses in peripheral blood mononuclear cells of a sensitized atopic dermatitis patient. As has been proposed for environmental allergens it is possible that T cell responses to IgE-defined autoantigens may contribute to the chronic skin manifestations in atopic dermatitis.
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[Anonymous], ACTA DERM VENERE S92, DOI [10.2340/00015555924447, DOI 10.2340/00015555924447]
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UNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USAUNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USA
FLING, SP
GREGERSON, DS
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UNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USAUNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USA
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UNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USAUNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USA
FLING, SP
GREGERSON, DS
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h-index: 0
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UNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USAUNIV MINNESOTA, SCH MED,DEPT OPHTHALMOL,493 MAYO MEM BLDG, 516 DELAWARE ST SE, MINNEAPOLIS, MN 55455 USA