Literature DB >> 29501325

Protein Disaggregation in Multicellular Organisms.

Nadinath B Nillegoda1, Anne S Wentink2, Bernd Bukau3.   

Abstract

Protein aggregates are formed in cells with profoundly perturbed proteostasis, where the generation of misfolded proteins exceeds the cellular refolding and degradative capacity. They are a hallmark of protein conformational disorders and aged and/or environmentally stressed cells. Protein aggregation is a reversible process in vivo, which counteracts proteotoxicities derived from aggregate persistence, but the chaperone machineries involved in protein disaggregation in Metazoa were uncovered only recently. Here we highlight recent advances in the mechanistic understanding of the major protein disaggregation machinery mediated by the Hsp70 chaperone system and discuss emerging alternative disaggregation activities in multicellular organisms.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Caenorhabditis elegans; Hsp110; Hsp40; Hsp70; J-protein; aggregate solubilization; amyloid; chaperone; human; metazoan; protein aggregate; protein conformational disorders; protein disaggregation

Mesh:

Substances:

Year:  2018        PMID: 29501325     DOI: 10.1016/j.tibs.2018.02.003

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  41 in total

Review 1.  Targeting Hsp70 facilitated protein quality control for treatment of polyglutamine diseases.

Authors:  Amanda K Davis; William B Pratt; Andrew P Lieberman; Yoichi Osawa
Journal:  Cell Mol Life Sci       Date:  2019-09-24       Impact factor: 9.261

2.  Hsp104 facilitates the endoplasmic-reticulum-associated degradation of disease-associated and aggregation-prone substrates.

Authors:  Lynley M Doonan; Christopher J Guerriero; G Michael Preston; Teresa M Buck; Netaly Khazanov; Edward A Fisher; Hanoch Senderowitz; Jeffrey L Brodsky
Journal:  Protein Sci       Date:  2019-05-20       Impact factor: 6.725

Review 3.  Small heat shock proteins: Simplicity meets complexity.

Authors:  Martin Haslbeck; Sevil Weinkauf; Johannes Buchner
Journal:  J Biol Chem       Date:  2018-10-31       Impact factor: 5.157

4.  Function, evolution, and structure of J-domain proteins.

Authors:  Harm H Kampinga; Claes Andreasson; Alessandro Barducci; Michael E Cheetham; Douglas Cyr; Cecilia Emanuelsson; Pierre Genevaux; Jason E Gestwicki; Pierre Goloubinoff; Jaime Huerta-Cepas; Janine Kirstein; Krzysztof Liberek; Matthias P Mayer; Kazuhiro Nagata; Nadinath B Nillegoda; Pablo Pulido; Carlos Ramos; Paolo De Los Rios; Sabine Rospert; Rina Rosenzweig; Chandan Sahi; Mikko Taipale; Bratłomiej Tomiczek; Ryo Ushioda; Jason C Young; Richard Zimmermann; Alicja Zylicz; Maciej Zylicz; Elizabeth A Craig; Jaroslaw Marszalek
Journal:  Cell Stress Chaperones       Date:  2018-11-26       Impact factor: 3.667

Review 5.  Hsp70 molecular chaperones: multifunctional allosteric holding and unfolding machines.

Authors:  Eugenia M Clerico; Wenli Meng; Alexandra Pozhidaeva; Karishma Bhasne; Constantine Petridis; Lila M Gierasch
Journal:  Biochem J       Date:  2019-06-14       Impact factor: 3.857

Review 6.  Not quite the SSAme: unique roles for the yeast cytosolic Hsp70s.

Authors:  Sarah K Lotz; Laura E Knighton; Gary W Jones; Andrew W Truman
Journal:  Curr Genet       Date:  2019-04-24       Impact factor: 3.886

7.  Structural basis for client recognition and activity of Hsp40 chaperones.

Authors:  Yajun Jiang; Paolo Rossi; Charalampos G Kalodimos
Journal:  Science       Date:  2019-09-20       Impact factor: 47.728

Review 8.  Modulation of Amyloid States by Molecular Chaperones.

Authors:  Anne Wentink; Carmen Nussbaum-Krammer; Bernd Bukau
Journal:  Cold Spring Harb Perspect Biol       Date:  2019-07-01       Impact factor: 10.005

9.  Host expression system modulates recombinant Hsp70 activity through post-translational modifications.

Authors:  Mauricio M Rigo; Thiago J Borges; Benjamin J Lang; Ayesha Murshid; Donald Wolfgeher; Stuart K Calderwood; Andrew W Truman; Cristina Bonorino
Journal:  FEBS J       Date:  2020-03-06       Impact factor: 5.542

10.  Targeting the interaction of AIMP2-DX2 with HSP70 suppresses cancer development.

Authors:  Semi Lim; Hye Young Cho; Dae Gyu Kim; Younah Roh; Se-Young Son; Ameeq Ul Mushtaq; Minkyoung Kim; Deepak Bhattarai; Aneesh Sivaraman; Youngjin Lee; Jihye Lee; Won Suk Yang; Hoi Kyoung Kim; Myung Hee Kim; Kyeong Lee; Young Ho Jeon; Sunghoon Kim
Journal:  Nat Chem Biol       Date:  2019-12-02       Impact factor: 15.040

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