Literature DB >> 28696498

Hsp70 - a master regulator in protein degradation.

María Rosario Fernández-Fernández1, Marcos Gragera1, Lissette Ochoa-Ibarrola1, Lucía Quintana-Gallardo1, José María Valpuesta1.   

Abstract

Proteostasis, the controlled balance of protein synthesis, folding, assembly, trafficking and degradation, is a paramount necessity for cell homeostasis. Impaired proteostasis is a hallmark of ageing and of many human diseases. Molecular chaperones are essential for proteostasis in eukaryotic cells, and their function has traditionally been linked to protein folding, assembly and disaggregation. More recent findings suggest that chaperones also contribute to key steps in protein degradation. In particular, Hsp70 has an essential role in substrate degradation through the ubiquitin-proteasome system, as well as through different autophagy pathways. Accumulated knowledge suggests that the fate of an Hsp70 substrate is dictated by the combination of partners (cochaperones and other chaperones) that interact with Hsp70 in a given cell context.
© 2017 Federation of European Biochemical Societies.

Entities:  

Keywords:  Hsp70; protein degradation; proteostasis

Mesh:

Substances:

Year:  2017        PMID: 28696498     DOI: 10.1002/1873-3468.12751

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  51 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

Review 2.  Recent advances in the structural and mechanistic aspects of Hsp70 molecular chaperones.

Authors:  Matthias P Mayer; Lila M Gierasch
Journal:  J Biol Chem       Date:  2018-11-19       Impact factor: 5.157

3.  Inverse Correlation Between MPSR1 E3 Ubiquitin Ligase and HSP90.1 Balances Cytoplasmic Protein Quality Control.

Authors:  Jong Hum Kim; Tae Rin Oh; Seok Keun Cho; Seong Wook Yang; Woo Taek Kim
Journal:  Plant Physiol       Date:  2019-03-19       Impact factor: 8.340

Review 4.  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

5.  An unexpected second binding site for polypeptide substrates is essential for Hsp70 chaperone activity.

Authors:  Hongtao Li; Huanyu Zhu; Evans Boateng Sarbeng; Qingdai Liu; Xueli Tian; Ying Yang; Charles Lyons; Lei Zhou; Qinglian Liu
Journal:  J Biol Chem       Date:  2019-12-05       Impact factor: 5.157

6.  KLR-70: A Novel Cationic Inhibitor of the Bacterial Hsp70 Chaperone.

Authors:  Matthew D Dalphin; Andrew J Stangl; Yue Liu; Silvia Cavagnero
Journal:  Biochemistry       Date:  2020-05-04       Impact factor: 3.162

Review 7.  Structural and functional analysis of the Hsp70/Hsp40 chaperone system.

Authors:  Qinglian Liu; Ce Liang; Lei Zhou
Journal:  Protein Sci       Date:  2019-10-07       Impact factor: 6.725

Review 8.  Modulating protein-protein interaction networks in protein homeostasis.

Authors:  Mengqi Zhong; Gregory M Lee; Eline Sijbesma; Christian Ottmann; Michelle R Arkin
Journal:  Curr Opin Chem Biol       Date:  2019-03-23       Impact factor: 8.822

Review 9.  Post-translational modifications of Hsp70 family proteins: Expanding the chaperone code.

Authors:  Corey M Porter; Andrew W Truman; Matthias C Truttmann
Journal:  J Biol Chem       Date:  2020-06-09       Impact factor: 5.157

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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