Literature DB >> 19491934

Converging concepts of protein folding in vitro and in vivo.

F Ulrich Hartl1, Manajit Hayer-Hartl.   

Abstract

Most proteins must fold into precise three-dimensional conformations to fulfill their biological functions. Here we review recent concepts emerging from studies of protein folding in vitro and in vivo, with a focus on how proteins navigate the complex folding energy landscape inside cells with the aid of molecular chaperones. Understanding these reactions is also of considerable medical relevance, as the aggregation of misfolding proteins that escape the cellular quality-control machinery underlies a range of debilitating diseases, including many age-onset neurodegenerative disorders.

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Year:  2009        PMID: 19491934     DOI: 10.1038/nsmb.1591

Source DB:  PubMed          Journal:  Nat Struct Mol Biol        ISSN: 1545-9985            Impact factor:   15.369


  104 in total

Review 1.  Folding of newly translated proteins in vivo: the role of molecular chaperones.

Authors:  J Frydman
Journal:  Annu Rev Biochem       Date:  2001       Impact factor: 23.643

Review 2.  Chaperonin-mediated protein folding.

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

Review 3.  Protein folding and misfolding.

Authors:  Christopher M Dobson
Journal:  Nature       Date:  2003-12-18       Impact factor: 49.962

Review 4.  Inter-residue interactions in protein folding and stability.

Authors:  M Michael Gromiha; S Selvaraj
Journal:  Prog Biophys Mol Biol       Date:  2004-10       Impact factor: 3.667

5.  Systems analyses reveal two chaperone networks with distinct functions in eukaryotic cells.

Authors:  Véronique Albanèse; Alice Yen-Wen Yam; Joshua Baughman; Charles Parnot; Judith Frydman
Journal:  Cell       Date:  2006-01-13       Impact factor: 41.582

6.  GroEL stimulates protein folding through forced unfolding.

Authors:  Zong Lin; Damian Madan; Hays S Rye
Journal:  Nat Struct Mol Biol       Date:  2008-03-02       Impact factor: 15.369

7.  Insights into Hsp70 chaperone activity from a crystal structure of the yeast Hsp110 Sse1.

Authors:  Qinglian Liu; Wayne A Hendrickson
Journal:  Cell       Date:  2007-10-05       Impact factor: 41.582

8.  Crystal structure of the nucleotide exchange factor GrpE bound to the ATPase domain of the molecular chaperone DnaK.

Authors:  C J Harrison; M Hayer-Hartl; M Di Liberto; F Hartl; J Kuriyan
Journal:  Science       Date:  1997-04-18       Impact factor: 47.728

9.  Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease.

Authors:  A Sittler; R Lurz; G Lueder; J Priller; H Lehrach; M K Hayer-Hartl; F U Hartl; E E Wanker
Journal:  Hum Mol Genet       Date:  2001-06-01       Impact factor: 6.150

10.  Cellular mechanisms of membrane protein folding.

Authors:  William R Skach
Journal:  Nat Struct Mol Biol       Date:  2009-06       Impact factor: 15.369

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  418 in total

Review 1.  HSP90 at the hub of protein homeostasis: emerging mechanistic insights.

Authors:  Mikko Taipale; Daniel F Jarosz; Susan Lindquist
Journal:  Nat Rev Mol Cell Biol       Date:  2010-06-09       Impact factor: 94.444

2.  Study on the chaperone properties of conserved GTPases.

Authors:  Xiang Wang; Jiaying Xue; Zhe Sun; Yan Qin; Weimin Gong
Journal:  Protein Cell       Date:  2012-01-13       Impact factor: 14.870

3.  Knot formation in newly translated proteins is spontaneous and accelerated by chaperonins.

Authors:  Anna L Mallam; Sophie E Jackson
Journal:  Nat Chem Biol       Date:  2011-12-18       Impact factor: 15.040

4.  Unique peptide substrate binding properties of 110-kDa heat-shock protein (Hsp110) determine its distinct chaperone activity.

Authors:  Xinping Xu; Evans Boateng Sarbeng; Christina Vorvis; Divya Prasanna Kumar; Lei Zhou; Qinglian Liu
Journal:  J Biol Chem       Date:  2011-12-08       Impact factor: 5.157

5.  Kinetic analysis of ribosome-bound fluorescent proteins reveals an early, stable, cotranslational folding intermediate.

Authors:  Devaki A Kelkar; Amardeep Khushoo; Zhongying Yang; William R Skach
Journal:  J Biol Chem       Date:  2011-11-28       Impact factor: 5.157

6.  A mystery unfolds: Franz-Ulrich Hartl and Arthur L. Horwich win the 2011 Albert Lasker Basic Medical Research Award.

Authors:  Kathryn Claiborn
Journal:  J Clin Invest       Date:  2011-10       Impact factor: 14.808

7.  Structural and functional insights into TRiC chaperonin from a psychrophilic yeast, Glaciozyma antarctica.

Authors:  Nur Athirah Yusof; Shazilah Kamaruddin; Farah Diba Abu Bakar; Nor Muhammad Mahadi; Abdul Munir Abdul Murad
Journal:  Cell Stress Chaperones       Date:  2019-01-16       Impact factor: 3.667

Review 8.  Macromolecular Crowding In Vitro, In Vivo, and In Between.

Authors:  Germán Rivas; Allen P Minton
Journal:  Trends Biochem Sci       Date:  2016-09-23       Impact factor: 13.807

9.  Simulations and Experiments Delineate Amyloid Fibrilization by Peptides Derived from Glaucoma-Associated Myocilin.

Authors:  Yiming Wang; Yuan Gao; Shannon E Hill; Dustin J E Huard; Moya O Tomlin; Raquel L Lieberman; Anant K Paravastu; Carol K Hall
Journal:  J Phys Chem B       Date:  2018-05-21       Impact factor: 2.991

10.  The DNAJA2 substrate release mechanism is essential for chaperone-mediated folding.

Authors:  Imad Baaklini; Michael J H Wong; Christine Hantouche; Yogita Patel; Alvin Shrier; Jason C Young
Journal:  J Biol Chem       Date:  2012-10-22       Impact factor: 5.157

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