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

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第一作者： Lynley M,Doonan

第一单位： Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, 15260.

作者： Lynley M,Doonan ^[1] ; Christopher J,Guerriero ^[1] ; G Michael,Preston ^[1] ; Teresa M,Buck ^[1] ; Netaly,Khazanov ^[2] ; Edward A,Fisher ^[3] ; Hanoch,Senderowitz ^[2] ; Jeffrey L,Brodsky ^[1]

作者单位： Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, 15260. ^[1] Department of Chemistry, Bar Ilan University, Ramat Gan, 5290002, Israel. ^[2] Division of Cardiology, Department of Medicine and Cell Biology, New York University, New York, New York, 10016. ^[3]

关键词 AAA-ATPase Hsp104 apolipoprotein B cystic fibrosis transmembrane conductance regulator endoplasmic-reticulum-associated degradation molecular chaperone proteasome protein aggregation ubiquitin yeast

主题词内质网(Endoplasmic Reticulum);热休克蛋白质类(Heat-Shock Proteins);分子伴侣(Molecular Chaperones);分子动力学模拟(Molecular Dynamics Simulation);突变(Mutation);酿酒酵母蛋白质类(Saccharomyces cerevisiae Proteins)

DOI 10.1002/pro.3636

PMID 31050848

发布时间 2021-02-17

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