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No acceleration of rhodanese refolding by tail-multiplied variants of SR1. Guanidine-HCl-denatured rhodanese was diluted into buffer containing the indicated chaperonin to form a binary complex. GroES and ATP were added, and at the indicated times, the recovery of native protein was measured by assay of rhodanese enzymatic activity. The amount of native rhodanese recovered is expressed as a percentage of the total input rhodanese.
