Literature DB >> 25887400

Effects of C-terminal Truncation of Chaperonin GroEL on the Yield of In-cage Folding of the Green Fluorescent Protein.

So Ishino1, Yasushi Kawata2, Hideki Taguchi3, Naoko Kajimura4, Katsumi Matsuzaki1, Masaru Hoshino5.   

Abstract

Chaperonin GroEL from Escherichia coli consists of two heptameric rings stacked back-to-back to form a cagelike structure. It assists in the folding of substrate proteins in concert with the co-chaperonin GroES by incorporating them into its large cavity. The mechanism underlying the incorporation of substrate proteins currently remains unclear. The flexible C-terminal residues of GroEL, which are invisible in the x-ray crystal structure, have recently been suggested to play a key role in the efficient encapsulation of substrates. These C-terminal regions have also been suggested to separate the double rings of GroEL at the bottom of the cavity. To elucidate the role of the C-terminal regions of GroEL on the efficient encapsulation of substrate proteins, we herein investigated the effects of C-terminal truncation on GroE-mediated folding using the green fluorescent protein (GFP) as a substrate. We demonstrated that the yield of in-cage folding mediated by a single ring GroEL (SR1) was markedly decreased by truncation, whereas that mediated by a double ring football-shaped complex was not affected. These results suggest that the C-terminal region of GroEL functions as a barrier between rings, preventing the leakage of GFP through the bottom space of the cage. We also found that once GFP folded into its native conformation within the cavity of SR1 it never escaped even in the absence of the C-terminal tails. This suggests that GFP molecules escaped through the pore only when they adopted a denatured conformation. Therefore, the folding and escape of GFP from C-terminally truncated SR1·GroES appeared to be competing with each other.
© 2015 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  ATP; Escherichia coli (E. coli); fluorescence; molecular chaperone; protein folding

Mesh:

Substances:

Year:  2015        PMID: 25887400      PMCID: PMC4463448          DOI: 10.1074/jbc.M114.633636

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


  38 in total

1.  Structural features of the GroEL-GroES nano-cage required for rapid folding of encapsulated protein.

Authors:  Yun-Chi Tang; Hung-Chun Chang; Annette Roeben; Dirk Wischnewski; Nadine Wischnewski; Michael J Kerner; F Ulrich Hartl; Manajit Hayer-Hartl
Journal:  Cell       Date:  2006-06-02       Impact factor: 41.582

2.  Hydrophilic residues 526 KNDAAD 531 in the flexible C-terminal region of the chaperonin GroEL are critical for substrate protein folding within the central cavity.

Authors:  Kodai Machida; Akane Kono-Okada; Kunihiro Hongo; Tomohiro Mizobata; Yasushi Kawata
Journal:  J Biol Chem       Date:  2008-01-09       Impact factor: 5.157

3.  The C-terminal tails of the bacterial chaperonin GroEL stimulate protein folding by directly altering the conformation of a substrate protein.

Authors:  Jeremy Weaver; Hays S Rye
Journal:  J Biol Chem       Date:  2014-06-25       Impact factor: 5.157

4.  Formation and structures of GroEL:GroES2 chaperonin footballs, the protein-folding functional form.

Authors:  Xue Fei; Xiang Ye; Nicole A LaRonde; George H Lorimer
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-18       Impact factor: 11.205

5.  Crystal structure of a symmetric football-shaped GroEL:GroES2-ATP14 complex determined at 3.8Å reveals rearrangement between two GroEL rings.

Authors:  Ayumi Koike-Takeshita; Takatoshi Arakawa; Hideki Taguchi; Tatsuro Shimamura
Journal:  J Mol Biol       Date:  2014-08-28       Impact factor: 5.469

6.  Evaluation of the stability of an SR398/GroES chaperonin complex.

Authors:  So Ishino; Yasushi Kawata; Takahisa Ikegami; Katsumi Matsuzaki; Masaru Hoshino
Journal:  J Biochem       Date:  2014-02-21       Impact factor: 3.387

7.  Active cage mechanism of chaperonin-assisted protein folding demonstrated at single-molecule level.

Authors:  Amit J Gupta; Shubhasis Haldar; Goran Miličić; F Ulrich Hartl; Manajit Hayer-Hartl
Journal:  J Mol Biol       Date:  2014-05-06       Impact factor: 5.469

8.  Perturbed ATPase activity and not "close confinement" of substrate in the cis cavity affects rates of folding by tail-multiplied GroEL.

Authors:  George W Farr; Wayne A Fenton; Arthur L Horwich
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-19       Impact factor: 11.205

9.  The strongly conserved carboxyl-terminus glycine-methionine motif of the Escherichia coli GroEL chaperonin is dispensable.

Authors:  N F McLennan; A S Girshovich; N M Lissin; Y Charters; M Masters
Journal:  Mol Microbiol       Date:  1993-01       Impact factor: 3.501

Review 10.  Structure and function in GroEL-mediated protein folding.

Authors:  P B Sigler; Z Xu; H S Rye; S G Burston; W A Fenton; A L Horwich
Journal:  Annu Rev Biochem       Date:  1998       Impact factor: 23.643

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  2 in total

1.  Essential functions linked with structural disorder in organisms of minimal genome.

Authors:  Rita Pancsa; Peter Tompa
Journal:  Biol Direct       Date:  2016-09-08       Impact factor: 4.540

2.  Novel cryo-EM structure of an ADP-bound GroEL-GroES complex.

Authors:  Sofia S Kudryavtseva; Evgeny B Pichkur; Igor A Yaroshevich; Aleksandra A Mamchur; Irina S Panina; Andrei V Moiseenko; Olga S Sokolova; Vladimir I Muronetz; Tatiana B Stanishneva-Konovalova
Journal:  Sci Rep       Date:  2021-09-14       Impact factor: 4.379

  2 in total

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