Literature DB >> 28066979

When proteostasis goes bad: Protein aggregation in the cell.

Mona Radwan1, Rebecca J Wood1, Xiaojing Sui1, Danny M Hatters1.   

Abstract

Protein aggregation is a hallmark of the major neurodegenerative diseases including Alzheimer's, Parkinson's, Huntington's and motor neuron and is a symptom of a breakdown in the management of proteome foldedness. Indeed, it is remarkable that under normal conditions cells can keep their proteome in a highly crowded and confined space without uncontrollable aggregation. Proteins pose a particular challenge relative to other classes of biomolecules because upon synthesis they must typically follow a complex folding pathway to reach their functional conformation (native state). Non-native conformations, including the unfolded nascent chain, are highly prone to aberrant interactions, leading to aggregation. Here we review recent advances in knowledge of proteostasis, approaches to monitor proteostasis and the impact that protein aggregation has on biology. We also include discussion of the outstanding challenges.
© 2017 IUBMB Life, 69(2):49-54, 2017. © 2017 International Union of Biochemistry and Molecular Biology.

Entities:  

Keywords:  amyloid; chaperones; protein aggregation; protein folding; protein misfolding; protein quality control; proteostasis

Mesh:

Substances:

Year:  2017        PMID: 28066979     DOI: 10.1002/iub.1597

Source DB:  PubMed          Journal:  IUBMB Life        ISSN: 1521-6543            Impact factor:   3.885


  10 in total

Review 1.  Insights into protein misfolding and aggregation enabled by solid-state NMR spectroscopy.

Authors:  Patrick C A van der Wel
Journal:  Solid State Nucl Magn Reson       Date:  2017-10-04       Impact factor: 2.293

2.  Small Molecule Modulation of Proteasome Assembly.

Authors:  Evert Njomen; Pawel A Osmulski; Corey L Jones; Maria Gaczynska; Jetze J Tepe
Journal:  Biochemistry       Date:  2018-06-27       Impact factor: 3.162

Review 3.  Cellular Regulation of Amyloid Formation in Aging and Disease.

Authors:  Esther Stroo; Mandy Koopman; Ellen A A Nollen; Alejandro Mata-Cabana
Journal:  Front Neurosci       Date:  2017-02-14       Impact factor: 4.677

4.  Conformational flexibility within the nascent polypeptide-associated complex enables its interactions with structurally diverse client proteins.

Authors:  Esther M Martin; Matthew P Jackson; Martin Gamerdinger; Karina Gense; Theodoros K Karamonos; Julia R Humes; Elke Deuerling; Alison E Ashcroft; Sheena E Radford
Journal:  J Biol Chem       Date:  2018-04-12       Impact factor: 5.157

5.  Prolines Affect the Nucleation Phase of Amyloid Fibrillation Reaction; Mutational Analysis of Human Stefin B.

Authors:  Samra Hasanbašić; Ajda Taler-Verčič; Vida Puizdar; Veronika Stoka; Magda Tušek Žnidarič; Andrej Vilfan; Selma Berbić; Eva Žerovnik
Journal:  ACS Chem Neurosci       Date:  2019-04-09       Impact factor: 4.418

6.  Requirement for p62 acetylation in the aggregation of ubiquitylated proteins under nutrient stress.

Authors:  Zhiyuan You; Wen-Xue Jiang; Ling-Yun Qin; Zhou Gong; Wei Wan; Jin Li; Yusha Wang; Hongtao Zhang; Chao Peng; Tianhua Zhou; Chun Tang; Wei Liu
Journal:  Nat Commun       Date:  2019-12-19       Impact factor: 14.919

Review 7.  Protein Complexes Form a Basis for Complex Hybrid Incompatibility.

Authors:  Krishna B S Swamy; Scott C Schuyler; Jun-Yi Leu
Journal:  Front Genet       Date:  2021-02-09       Impact factor: 4.599

Review 8.  Proteostasis in the Male and Female Germline: A New Outlook on the Maintenance of Reproductive Health.

Authors:  Shenae L Cafe; Brett Nixon; Heath Ecroyd; Jacinta H Martin; David A Skerrett-Byrne; Elizabeth G Bromfield
Journal:  Front Cell Dev Biol       Date:  2021-04-16

9.  UXT chaperone prevents proteotoxicity by acting as an autophagy adaptor for p62-dependent aggrephagy.

Authors:  Min Ji Yoon; Boyoon Choi; Eun Jin Kim; Jiyeon Ohk; Chansik Yang; Yeon-Gil Choi; Jinyoung Lee; Chanhee Kang; Hyun Kyu Song; Yoon Ki Kim; Jae-Sung Woo; Yongcheol Cho; Eui-Ju Choi; Hosung Jung; Chungho Kim
Journal:  Nat Commun       Date:  2021-03-29       Impact factor: 14.919

10.  A thiol probe for measuring unfolded protein load and proteostasis in cells.

Authors:  Moore Z Chen; Nagaraj S Moily; Jessica L Bridgford; Rebecca J Wood; Mona Radwan; Trevor A Smith; Zhegang Song; Ben Zhong Tang; Leann Tilley; Xiaohong Xu; Gavin E Reid; Mahmoud A Pouladi; Yuning Hong; Danny M Hatters
Journal:  Nat Commun       Date:  2017-09-07       Impact factor: 14.919

  10 in total

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