Abstract

Reduced, denatured lysozyme tends to aggregate at neutral pH, and competition between productive folding and aggregation substantially reduces the efficiency of refolding (Goldberg, M.E., Rudolph, R., and Jaenicke, R. (1991) Biochemistry 30, 2790-2797). Protein disulfide isomerase (PDI), a catalyst of oxidative protein folding, has a variety of effects on the yield of native lysozyme during the oxidative refolding of the reduced, denatured protein. Depending on the concentration of lysozyme, the concentration of PDI, and the order in which lysozyme and PDI are added to initiate folding, PDI can produce a substantial increase or a substantial decrease in the recovery of native lysozyme, when compared with the uncatalyzed reaction. In the presence of a glutathione redox buffer, denatured lysozyme (1-10 microM) partitions almost equally between productive folding leading to native lysozyme (50-63%) and non-productive fates including the formation of disulfide cross-linked aggregates. At the higher lysozyme concentrations examined (5-10 microM), substoichiometric concentrations of PDI (0.5-1 microM) exhibit "anti-chaperone" activity; PDI actively diverts most of the denatured lysozyme away from productive folding so that only 17 +/- 9% of the lysozyme is recovered as native enzyme. PDI's anti-chaperone activity results in extensive intermolecular disulfide crosslinking of lysozyme into large, inactive aggregates. On the other hand, if PDI is initially present at a large molar excess (5-10-fold) when denatured lysozyme is diluted to initiate folding, PDI demonstrates a chaperone-like activity that prevents aggregate formation and promotes correct folding. When PDI's chaperone activity is dominant, virtually all of the denatured lysozyme is correctly folded. The schizophrenic chaperone/anti-chaperone nature of PDI activity accounts for a number of observations on in vivo protein folding, including the necessity for maintaining a high concentration of PDI in the endoplasmic reticulum and the formation of disulfide cross-linked aggregates in the endoplasmic reticulum during the expression of disulfide-containing proteins (deSilva, A., Braakman, I., and Helenius, A. (1993) J. Cell. Biol. 120, 647-655).

Highlights

  • In neutral pH, and competitionbetween productive folding and aggregation substantially reduces the efficiency of refolding

  • In thepresence of a glutathione redox buffer, denatured lysozyme (1-10PM) partitions almost between productive folding leading to native lysozyme (5043%) and non-productive fates including the formation of disulfide cross-linked aggregates

  • The disulfide isomerase activity increases the rate of lysozyme folding, but the increased folding rate is notnecessarily associated with an increase in the amount of lysozyme that folds productively

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Summary

Introduction

In neutral pH, and competitionbetween productive folding and aggregation substantially reduces the efficiency of refolding Molecular chaperones do not appreciably accelerate folding but bind to nonnative proteins in a way that is thoughtto inhibit non-productive aggregationand misfolding (2,5) Inorder to prevent these improper interactions, chaperones must be present at concentrations that are stoichiometric with newly synthesized proteins; they are often found at very high concentrationisnthe cell. When the activities of molecular chaperones and foldases become unbalanced, productive folding may be perturbed, often in unexpected ways.For example, over expression of BiP, the major ER chaperone, selectively inhibits the production of several secreted proteins (12), and over-expression of some disulfide-containing proteins leads to the formation of large aggregates that acrreoss-linked by intermolecular disulfide bonds (13,14).Making the ER tooreducing to support

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