| Literature DB >> 1904085 |
M A Bednarek1, S A Engl, M C Gammon, J A Lindquist, G Porter, A R Williamson, H J Zweerink.
Abstract
The influenza A virus matrix protein derived peptide with amino acids 57-68 (Lys-Gly-Ileu-Leu-Gly-Phe-Val-Phe-Thr-Leu-Thr-Val) is recognized by influenza virus HLA-A2 restricted CTL. Because of the large number of hydrophobic residues this peptide is very insoluble. Substitution with a number of polar amino acids resulted in a soluble peptide (Lys-Lys-Ala-Leu-Gly-Phe-Val-Phe-Thr-Leu-Asp-Lys) that was very effective in sensitizing HLA-A2 positive target cells. Further substitution of threonine in position 65 with lysine resulted in a soluble antagonist peptide that inhibited sensitization. Both agonist and antagonist peptides retained 20% of their biological activity when tyrosine was added at the N terminus. Soluble radio-iodinated peptides can now be prepared that will be useful reagents to study the interaction of peptides and class I molecules.Entities:
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Year: 1991 PMID: 1904085 DOI: 10.1016/0022-1759(91)90349-k
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303