Literature DB >> 7986648

Transmission electron microscopy of GroEL, GroES, and the symmetrical GroEL/ES complex.

J R Harris1, A Plückthun, R Zahn.   

Abstract

Two new 2-D crystal forms of the Escherichia coli chaperone GroEL (cpn60) 2 x 7-mer have been produced using the negative staining-carbon film (NS-CF) technique. These 2-D crystals, which contain the cylindrical GroEL in side-on and end-on orientations, both possess p21 symmetry, with two molecules in the respective unit cells. The crystallographically averaged images correlate well with those obtained by other authors from single particle analysis of GroEL and our own previous crystallographic analysis. 2-D crystallization of the smaller chaperone GroES (cpn10) 7-mer has also been achieved using the NS-CF technique. Crystallographically averaged images of GroES single particle images indicate considerable variation in molecular shape, which is most likely due to varying molecular orientation on the carbon support film. The quaternary structure of GroES does, nevertheless, approximate to a ring-like shape. The complex formed by GroEL and GroES in the presence of ATP at room temperature has been shown to possess a symmetrical hollow ellipsoidal conformation. This symmetrical complex forms in the presence of a 2:1 or greater molar ratio of GroES:GroEL. At lower molar ratios linear chains of GroEL form, apparently linked by GroES in a 1:1 manner, which provide supportive evidence for the ability of both ends of the GroEL cylinder to interact with GroES. The apparent discrepancy between our data and that of other groups who have described an asymmetrical "bullet-shaped" (holo-chaperone) GroEL/ES complex is discussed in detail.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7986648     DOI: 10.1006/jsbi.1994.1022

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  10 in total

1.  Significance of chaperonin 10-mediated inhibition of ATP hydrolysis by chaperonin 60.

Authors:  Y Dubaquié; R Looser; S Rospert
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

2.  The opening of the SPP1 bacteriophage tail, a prevalent mechanism in Gram-positive-infecting siphophages.

Authors:  Adeline Goulet; Joséphine Lai-Kee-Him; David Veesler; Isabelle Auzat; Gautier Robin; Dale A Shepherd; Alison E Ashcroft; Eric Richard; Julie Lichière; Paulo Tavares; Christian Cambillau; Patrick Bron
Journal:  J Biol Chem       Date:  2011-05-26       Impact factor: 5.157

3.  Chaperonins GroEL and GroES: views from atomic force microscopy.

Authors:  J Mou; S Sheng; R Ho; Z Shao
Journal:  Biophys J       Date:  1996-10       Impact factor: 4.033

4.  Reconciling the controversy regarding the functional importance of bullet- and football-shaped GroE complexes.

Authors:  Lavi S Bigman; Amnon Horovitz
Journal:  J Biol Chem       Date:  2019-08-01       Impact factor: 5.157

5.  Crystallization and structure determination of a symmetrical 'football' complex of the mammalian mitochondrial Hsp60-Hsp10 chaperonins.

Authors:  Shahar Nisemblat; Avital Parnas; Oren Yaniv; Abdussalam Azem; Felix Frolow
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2013-12-24       Impact factor: 1.056

6.  The protein-folding activity of chaperonins correlates with the symmetric GroEL14(GroES7)2 heterooligomer.

Authors:  A Azem; S Diamant; M Kessel; C Weiss; P Goloubinoff
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-19       Impact factor: 11.205

7.  Integrated self-assembly of the Mms6 magnetosome protein to form an iron-responsive structure.

Authors:  Shuren Feng; Lijun Wang; Pierre Palo; Xunpei Liu; Surya K Mallapragada; Marit Nilsen-Hamilton
Journal:  Int J Mol Sci       Date:  2013-07-12       Impact factor: 5.923

Review 8.  Dynamic Complexes in the Chaperonin-Mediated Protein Folding Cycle.

Authors:  Celeste Weiss; Fady Jebara; Shahar Nisemblat; Abdussalam Azem
Journal:  Front Mol Biosci       Date:  2016-12-08

Review 9.  Chloroplast Chaperonin: An Intricate Protein Folding Machine for Photosynthesis.

Authors:  Qian Zhao; Cuimin Liu
Journal:  Front Mol Biosci       Date:  2018-01-19

10.  Back to GroEL-Assisted Protein Folding: GroES Binding-Induced Displacement of Denatured Proteins from GroEL to Bulk Solution.

Authors:  Victor Marchenkov; Andrey Gorokhovatsky; Natalia Marchenko; Tanya Ivashina; Gennady Semisotnov
Journal:  Biomolecules       Date:  2020-01-20
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.