Abstract
The amino acid motif QKRAA, when expressed on HLA-DRB1, carries susceptibility to develop rheumatoid arthritis. This motif is the basis of strong B and T cell epitopes. Furthermore, it is highly overrepresented in protein databases, suggesting that it carries a function of its own. To identify this function, we used QKRAA peptide affinity columns to screen total protein extracts from Escherichia coli. We found that DnaK, the E. coli 70-kD heat shock protein, binds QKRAA. Of interest, DnaK has a natural ligand, DnaJ, that contains a QKRAA motif. We found that QKRAA-containing peptides inhibit the binding of DnaK to DnaJ. Furthermore, rabbit antibody to the QKRAA motif can inhibit binding of DnaJ to DnaK.
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Auger, I., & Roudier, J. (1997). A function for the QKRAA amino acid motif: Mediating binding of DnaJ to DnaK. Implications for the association of rheumatoid arthritis with HLA-DR4. Journal of Clinical Investigation, 99(8), 1818–1822. https://doi.org/10.1172/JCI119348
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