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The chaperonin GroEL binds folding intermediates of four-disulfidehen lysozyme transiently within its central cavity. Using stopped flow fluorescence we show that GroEL binds early intermediates in folding and accelerates the slow kinetic phase that reflects the reversal of non-native interactions involving tryptophan residues and the formation of the native state. Pulsed hydrogen exchange monitored by electrospray ionization mass spectrometry demonstrates that GroEL does not alter the folding mechanism, nor are protected species unfolded by the chaperonin. The data suggest a mechanism for GroEL-assisted folding in which the reorganization of non-native tertiary interactions is facilitated but domain folding is unperturbed.

Original publication

DOI

10.1038/10735

Type

Journal article

Journal

Nat Struct Biol

Publication Date

07/1999

Volume

6

Pages

683 - 690

Keywords

Animals, Chaperonin 60, Chick Embryo, Dose-Response Relationship, Drug, Kinetics, Mass Spectrometry, Models, Biological, Muramidase, Protein Folding, Time Factors