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The chaperone DNAJB6 can suppress fibril formation of amyloid-β. This is dependent on functionally important conserved serine (S) and threonine (T) residues located in a C-terminal domain which is dominated by β-strands. Substitution of the conserved ST-residues with alanine residues results in loss of this function. In this thesis two DNAJB6 mimic constructs are examined to see whether or not the
