Literature DB >> 7909810

The effect of groES on the groEL-dependent assembly of dodecameric glutamine synthetase in the presence of ATP and ADP.

M T Fisher1.   

Abstract

The yields of active dodecameric glutamine synthetase (GS) are significantly increased when in vitro folding is initiated in the presence of the Escherichia coli groE chaperonins and ATP (37 degrees C). To observe the effects of chaperonins and ATP on GS assembly, the GS assembly intermediates were separated by nondenaturing gel electrophoresis, visualized by Western analysis, and studied as a function of time. The form of GS that was initially released from groEL is monomeric. After the monomers formed dimers, active GS oligomers were assembled by the association of assembly competent dimers with higher order even-numbered oligomers until the dodecamer was formed. When ATP was added to the groEL.GS complex (no groES), a groEL.GS complex remained visible for up to 30 min after the renaturation was initiated. This slow disappearance of the groEL.GS complex is consistent with observed lags in both the GS activity regain profile and the assembly-dependent increase in GS tryptophan fluorescence. When groES was present, the addition of ATP resulted in the disappearance of observable complex at early sample times (< 2 min). Concomitantly, the rates of the regain of GS activity and the GS-dependent increase in tryptophan fluorescence intensity showed substantial accelerations. These results indicate that groES facilitates GS assembly from groEL by inducing the rapid release of GS from groEL, which in turn increases the concentration of assembly competent GS monomers. In addition, groES can initiate renaturation of GS from the groEL.GS arrested complex in the presence of ADP. When chaperonin-dependent GS renaturation was initiated with ATP or ADP (> or = 2 mM), the rates were identical. Since ATP hydrolysis is not absolutely required, the combined binding energies of groES and ATP (or ADP) appear to be sufficient to weaken the binding affinity of groEL for GS subunits and facilitate the release and refolding of assembly competent GS monomers from groEL.

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Year:  1994        PMID: 7909810

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

Review 1.  Chaperonins.

Authors:  N A Ranson; H E White; H R Saibil
Journal:  Biochem J       Date:  1998-07-15       Impact factor: 3.857

2.  Minimal and optimal mechanisms for GroE-mediated protein folding.

Authors:  A P Ben-Zvi; J Chatellier; A R Fersht; P Goloubinoff
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

3.  Heteromeric assembly of the cytosolic glutamine synthetase polypeptides of Medicago truncatula: complementation of a glnA Escherichia coli mutant with a plant domain-swapped enzyme.

Authors:  H Carvalho; C Sunkel; R Salema; J V Cullimore
Journal:  Plant Mol Biol       Date:  1997-11       Impact factor: 4.076

4.  Chaperonin-assisted folding of glutamine synthetase under nonpermissive conditions: off-pathway aggregation propensity does not determine the co-chaperonin requirement.

Authors:  P A Voziyan; M T Fisher
Journal:  Protein Sci       Date:  2000-12       Impact factor: 6.725

5.  Thermal unfolding of dodecameric glutamine synthetase: inhibition of aggregation by urea.

Authors:  N J Nosworthy; A Ginsburg
Journal:  Protein Sci       Date:  1997-12       Impact factor: 6.725

6.  Misfolded forms of glyceraldehyde-3-phosphate dehydrogenase interact with GroEL and inhibit chaperonin-assisted folding of the wild-type enzyme.

Authors:  Oxana V Polyakova; Olivier Roitel; Regina A Asryants; Alexei A Poliakov; Guy Branlant; Vladimir I Muronetz
Journal:  Protein Sci       Date:  2005-03-01       Impact factor: 6.725

7.  Strategies for folding of affinity tagged proteins using GroEL and osmolytes.

Authors:  Hiroo Katayama; Mitchell McGill; Andrew Kearns; Marek Brzozowski; Nicholas Degner; Bliss Harnett; Boris Kornilayev; Dubravka Matković-Calogović; Todd Holyoak; James P Calvet; Edward P Gogol; John Seed; Mark T Fisher
Journal:  J Struct Funct Genomics       Date:  2008-12-12

8.  Protein folding on biosensor tips: folding of maltodextrin glucosidase monitored by its interactions with GroEL.

Authors:  Ashutosh Pastor; Amit K Singh; Mark T Fisher; Tapan K Chaudhuri
Journal:  FEBS J       Date:  2016-08-01       Impact factor: 5.542

9.  Urea-induced dissociation and unfolding of dodecameric glutamine synthetase from Escherichia coli: calorimetric and spectral studies.

Authors:  M Zolkiewski; N J Nosworthy; A Ginsburg
Journal:  Protein Sci       Date:  1995-08       Impact factor: 6.725

  9 in total

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