J-domain proteins interaction with neurodegenerative disease-related proteins

被引:14
作者
Mariscal, Sara Maria Ayala [1 ]
Kirstein, Janine [1 ,2 ]
机构
[1] Forsch Verbund Berlin eV, Leibniz Res Inst Mol Pharmacol, R Roessle Str 10, D-13125 Berlin, Germany
[2] Univ Bremen, Cell Biol, Fac2, Leobener Str, D-28359 Bremen, Germany
关键词
J-domain proteins; Molecular chaperones; Neurodegenerative diseases; Amyloid proteins; Protein folding; Substrate binding;
D O I
10.1016/j.yexcr.2021.112491
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
HSP70 chaperones, J-domain proteins (JDPs) and nucleotide exchange factors (NEF) form functional networks that have the ability to prevent and reverse the aggregation of proteins associated with neurodegenerative diseases. JDPs can interact with specific substrate proteins, hold them in a refolding-competent conformation and target them to specific HSP70 chaperones for remodeling. Thereby, JDPs select specific substrates and constitute an attractive target for pharmacological intervention of neurodegenerative diseases. This, under the condition that the exact mechanism of JDPs interaction with specific substrates is unveiled. In this review, we provide an overview of the structural and functional variety of JDPs that interact with neurodegenerative disease-associated proteins and we highlight those studies that identified specific residues, domains or regions of JDPs that are crucial for substrate binding.
引用
收藏
页数:9
相关论文
共 86 条
[1]   DnaJA1 Antagonizes Constitutive Hsp70-Mediated Stabilization of Tau [J].
Abisambra, Jose F. ;
Jinwal, Umesh K. ;
Suntharalingam, Amirthaa ;
Arulselvam, Karthik ;
Brady, Sarah ;
Cockman, Matthew ;
Jin, Ying ;
Zhang, Bo ;
Dickey, Chad A. .
JOURNAL OF MOLECULAR BIOLOGY, 2012, 421 (4-5) :653-661
[2]  
Agarraberes FA, 2001, J CELL SCI, V114, P2491
[3]   The molecular chaperones DNAJB6 and Hsp70 cooperate to suppress α-synuclein aggregation [J].
Aprile, Francesco A. ;
Kallstig, Emma ;
Limorenko, Galina ;
Vendruscolo, Michele ;
Ron, David ;
Hansen, Christian .
SCIENTIFIC REPORTS, 2017, 7
[4]   Adapting proteostasis for disease intervention [J].
Balch, William E. ;
Morimoto, Richard I. ;
Dillin, Andrew ;
Kelly, Jeffery W. .
SCIENCE, 2008, 319 (5865) :916-919
[5]   In vivo aspects of protein folding and quality control [J].
Balchin, David ;
Hayer-Hartl, Manajit ;
Hartl, F. Ulrich .
SCIENCE, 2016, 353 (6294)
[6]   A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation [J].
Blumen, Sergiu C. ;
Astord, Stephanie ;
Robin, Valerie ;
Vignaud, Ludivine ;
Toumi, Nawel ;
Cieslik, Aurore ;
Achiron, Anat ;
Carasso, Ralph L. ;
Gurevich, Michael ;
Braverman, Itzhak ;
Blumen, Nava ;
Munich, Arnold ;
Barkats, Martine ;
Viollet, Louis .
ANNALS OF NEUROLOGY, 2012, 71 (04) :509-519
[7]  
Borges JC, 2012, PLOS ONE, V7, DOI [10.1371/journal.pone.0050927, 10.1371/journal.pone.0040447]
[8]   Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase [J].
Borrell-Pagès, M ;
Canals, JM ;
Cordelières, FP ;
Parker, JA ;
Pineda, JR ;
Grange, G ;
Bryson, EA ;
Guillermier, M ;
Hirsch, E ;
Hantraye, P ;
Cheetham, ME ;
Néri, C ;
Alberch, J ;
Brouillet, E ;
Saudou, F ;
Humbert, S .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (05) :1410-1424
[9]   A Chaperome Subnetwork Safeguards Proteostasis in Aging and Neurodegenerative Disease [J].
Brehme, Marc ;
Voisine, Cindy ;
Rolland, Thomas ;
Wachi, Shinichiro ;
Soper, James H. ;
Zhu, Yitan ;
Orton, Kai ;
Villella, Adriana ;
Garza, Dan ;
Vidal, Marc ;
Ge, Hui ;
Morimoto, Richard I. .
CELL REPORTS, 2014, 9 (03) :1135-1150
[10]   Yeast prions and human prion-like proteins: sequence features and prediction methods [J].
Cascarina, Sean M. ;
Ross, Eric D. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2014, 71 (11) :2047-2063