GroEL/GroES-mediated folding of a protein too large to be encapsulated.

Abstract:

:The chaperonin GroEL binds nonnative proteins too large to fit inside the productive GroEL-GroES cis cavity, but whether and how it assists their folding has remained unanswered. We have examined yeast mitochondrial aconitase, an 82 kDa monomeric Fe(4)S(4) cluster-containing enzyme, observed to aggregate in chaperonin-deficient mitochondria. We observed that aconitase folding both in vivo and in vitro requires both GroEL and GroES, and proceeds via multiple rounds of binding and release. Unlike the folding of smaller substrates, however, this mechanism does not involve cis encapsulation but, rather, requires GroES binding to the trans ring to release nonnative substrate, which likely folds in solution. Following the phase of ATP/GroES-dependent refolding, GroEL stably bound apoaconitase, releasing active holoenzyme upon Fe(4)S(4) cofactor formation, independent of ATP and GroES.

journal_name

Cell

journal_title

Cell

authors

Chaudhuri TK,Farr GW,Fenton WA,Rospert S,Horwich AL

doi

10.1016/s0092-8674(01)00523-2

subject

Has Abstract

pub_date

2001-10-19 00:00:00

pages

235-46

issue

2

eissn

0092-8674

issn

1097-4172

pii

S0092-8674(01)00523-2

journal_volume

107

pub_type

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