Production of Subtype-Specific Antipeptide Antibodies to Human Interferon-α1and -α4
- 1 June 1988
- journal article
- research article
- Published by Mary Ann Liebert Inc in Journal of Interferon Research
- Vol. 8 (3) , 325-332
- https://doi.org/10.1089/jir.1988.8.325
Abstract
Antibodies that are specific to the human interferon (IFN)-α1 and -α4 subtypes have been produced by immunizing rabbits with two short synthetic peptides, corresponding to residues 99-111 of IFN-α, and residues 37-50 of IFN-α4, respectively. The IFN-α, peptide has at least three closely clustered residues that are different from those in the other IFN-α subtypes, while the IFN-α4 peptide has only two unique amino acid residues, separated by five common residues. The antibodies raised against the IFN-α1 peptide react with recombinant human IFN-α1 but do not cross-react with recombinant human IFN-α4 or IFN-α2. The antibodies raised against the IFN-α4 peptide react with IFN-α4, crossreact with IFN-α1 but not with IFN-α2; the affinity of the antibodies to IFN-α1, however, is at least 10 times lower than their affinity to IFN-α4.This publication has 18 references indexed in Scilit:
- Automated Chemical Synthesis of a Protein Growth Factor for Hemopoietic Cells, Interleukin-3Science, 1986
- Intrinsic and Extrinsic Factors in Protein Antigenic StructureScience, 1985
- Structural relationship of human interferon alpha genes and pseudogenesJournal of Molecular Biology, 1985
- Immunochemical mapping of .alpha.-2 interferonBiochemistry, 1985
- Simplified DNA manupulations based on in vitro mutagenesisGene Analysis Techniques, 1985
- Monoclonal antibodies against subunits of yeast mitochondrial H+-ATPaseBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1984
- Mimicking the alloantigenicity of proteins with chemically synthesized peptides differing in single amino acidsNature, 1983
- The interferon genesBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1982
- Biochemistry of Interferons and Their ActionsAnnual Review of Biochemistry, 1982
- A new synthetic route to tert-butyloxycarbonylaminoacyl-4-(oxymethyl)phenylacetamidomethyl-resin, an improved support for solid-phase peptide synthesisThe Journal of Organic Chemistry, 1978