Literature DB >> 14615587

Conversion of the allosteric transition of GroEL from concerted to sequential by the single mutation Asp-155 -> Ala.

Oded Danziger1, Dalia Rivenzon-Segal, Sharon G Wolf, Amnon Horovitz.   

Abstract

The reaction cycle of the double-ring chaperonin GroEL is driven by ATP binding that takes place with positive cooperativity within each seven-membered ring and negative cooperativity between rings. The positive cooperativity within rings is due to ATP binding-induced conformational changes that are fully concerted. Herein, it is shown that the mutation Asp-155 --> Ala leads to an ATP-induced break in intra-ring and inter-ring symmetry. Electron microscopy analysis of single-ring GroEL particles containing the Asp-155 --> Ala mutation shows that the break in intra-ring symmetry is due to stabilization of allosteric intermediates such as one in which three subunits have switched their conformation while the other four have not. Our results show that eliminating an intra-subunit interaction between Asp-155 and Arg-395 results in conversion of the allosteric switch of GroEL from concerted to sequential, thus demonstrating that its allosteric behavior arises from coupled tertiary conformational changes.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14615587      PMCID: PMC283501          DOI: 10.1073/pnas.2333925100

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

1.  Synchronized domain-opening motion of GroEL is essential for communication between the two rings.

Authors:  K Shiseki; N Murai; F Motojima; T Hisabori; M Yoshida; H Taguchi
Journal:  J Biol Chem       Date:  2001-01-03       Impact factor: 5.157

2.  Chaperonin function: folding by forced unfolding.

Authors:  M Shtilerman; G H Lorimer; S W Englander
Journal:  Science       Date:  1999-04-30       Impact factor: 47.728

3.  ATP-bound states of GroEL captured by cryo-electron microscopy.

Authors:  N A Ranson; G W Farr; A M Roseman; B Gowen; W A Fenton; A L Horwich; H R Saibil
Journal:  Cell       Date:  2001-12-28       Impact factor: 41.582

4.  A 11.5 A single particle reconstruction of GroEL using EMAN.

Authors:  S J Ludtke; J Jakana; J L Song; D T Chuang; W Chiu
Journal:  J Mol Biol       Date:  2001-11-23       Impact factor: 5.469

Review 5.  Allostery and protein substrate conformational change during GroEL/GroES-mediated protein folding.

Authors:  H R Saibil; A L Horwich; W A Fenton
Journal:  Adv Protein Chem       Date:  2001

Review 6.  Chaperonin-mediated protein folding.

Authors:  D Thirumalai; G H Lorimer
Journal:  Annu Rev Biophys Biomol Struct       Date:  2001

7.  Nucleotide binding to the chaperonin GroEL: non-cooperative binding of ATP analogs and ADP, and cooperative effect of ATP.

Authors:  T Inobe; T Makio; E Takasu-Ishikawa; T P Terada; K Kuwajima
Journal:  Biochim Biophys Acta       Date:  2001-02-09

8.  The allosteric mechanism of the chaperonin GroEL: a dynamic analysis.

Authors:  J Ma; M Karplus
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

9.  Transient kinetic analysis of ATP-induced allosteric transitions in the eukaryotic chaperonin containing TCP-1.

Authors:  Galit Kafri; Amnon Horovitz
Journal:  J Mol Biol       Date:  2003-02-28       Impact factor: 5.469

Review 10.  Review: allostery in chaperonins.

Authors:  A Horovitz; Y Fridmann; G Kafri; O Yifrach
Journal:  J Struct Biol       Date:  2001-08       Impact factor: 2.867

View more
  15 in total

1.  Dynamics of allosteric transitions in GroEL.

Authors:  Changbong Hyeon; George H Lorimer; D Thirumalai
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-29       Impact factor: 11.205

2.  Concerted ATP-induced allosteric transitions in GroEL facilitate release of protein substrate domains in an all-or-none manner.

Authors:  Yakov Kipnis; Niv Papo; Gilad Haran; Amnon Horovitz
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-21       Impact factor: 11.205

3.  Crystal structure of a GroEL-ADP complex in the relaxed allosteric state at 2.7 Å resolution.

Authors:  Xue Fei; Dong Yang; Nicole LaRonde-LeBlanc; George H Lorimer
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-16       Impact factor: 11.205

Review 4.  Allostery and cooperativity revisited.

Authors:  Qiang Cui; Martin Karplus
Journal:  Protein Sci       Date:  2008-06-17       Impact factor: 6.725

5.  Concerted release of substrate domains from GroEL by ATP is demonstrated with FRET.

Authors:  Niv Papo; Yakov Kipnis; Gilad Haran; Amnon Horovitz
Journal:  J Mol Biol       Date:  2008-05-17       Impact factor: 5.469

Review 6.  The versatile mutational "repertoire" of Escherichia coli GroEL, a multidomain chaperonin nanomachine.

Authors:  Tomohiro Mizobata; Yasushi Kawata
Journal:  Biophys Rev       Date:  2017-11-27

Review 7.  Unpicking allosteric mechanisms of homo-oligomeric proteins by determining their successive ligand binding constants.

Authors:  Ranit Gruber; Amnon Horovitz
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2018-06-19       Impact factor: 6.237

8.  Football- and bullet-shaped GroEL-GroES complexes coexist during the reaction cycle.

Authors:  Tomoya Sameshima; Taro Ueno; Ryo Iizuka; Noriyuki Ishii; Naofumi Terada; Kohki Okabe; Takashi Funatsu
Journal:  J Biol Chem       Date:  2008-06-20       Impact factor: 5.157

9.  The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.

Authors:  Peter Bross; Søren Naundrup; Jakob Hansen; Marit Nyholm Nielsen; Jane Hvarregaard Christensen; Mogens Kruhøffer; Johan Palmfeldt; Thomas Juhl Corydon; Niels Gregersen; Debbie Ang; Costa Georgopoulos; Kåre Lehmann Nielsen
Journal:  J Biol Chem       Date:  2008-04-08       Impact factor: 5.157

10.  Perturbation-based Markovian transmission model for probing allosteric dynamics of large macromolecular assembling: a study of GroEL-GroES.

Authors:  Hsiao-Mei Lu; Jie Liang
Journal:  PLoS Comput Biol       Date:  2009-10-02       Impact factor: 4.475

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.