中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Acceleration of alpha-synuclein aggregation by homologous peptides

文献类型:期刊论文

作者Du, HN; Li, HT; Zhang, F; Lin, XJ; Shi, JH; Shi, YH; Ji, LN; Hu, J; Lin, DH; Hu, HY
刊名FEBS LETTERS
出版日期2006
卷号580期号:15页码:3657-3664
关键词alpha-synuclein GAV motif aggregation fibrillization homologous peptide Parkinson's disease
通讯作者Hu, HY (reprint author), Chinese Acad Sci, Key Lab Prote, Inst Biochem & Cell Biol, Shanghai Inst Biol Sci, Shanghai, Peoples R China.,hyhu@sibs.ac.cn
英文摘要alpha-Synuclein (alpha-Syn), amyloid beta-protein and prion protein are among the amyloidogenic proteins that are associated with the neurodegenerative diseases. These three proteins share a homologous region with a consensus sequence mainly consisting of glycine, alanine and valine residues (accordingly named as the GAV motif), which was proposed to be the critical core for the fibrillization and cytotoxicity. To understand the role of the GAV motif in protein amyloidogenesis, we studied the effects of the homologous peptides corresponding to the sequence of GAV motif region (residues 66-74) on alpha-Syn aggregation. The result shows that these peptides can promote fibrillization of wild-type a-Syn and induce that of the charge-incorporated mutants but not the GAV-deficient alpha-Syn mutant. The acceleration of a-Syn aggregation by the homologous peptides is under a sequence-specific manner. The interplay between the GAV peptide and the core regions in alpha-Syn may accelerate the aggregation process and stabilize the fibrils. This finding provides clues for developing peptide mimics that could promote transforming the toxic oligomers or protofibrils into the inert mature fibrils. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
学科主题Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
关键词[WOS]ABNORMAL PROTEIN AGGREGATION ; A-BETA COMPONENT ; ALZHEIMERS-DISEASE ; PARKINSONS-DISEASE ; PRION PROTEIN ; NEURODEGENERATIVE DISEASES ; AMYLOID FORMATION ; FIBRIL FORMATION ; LEWY BODIES ; SOLID-STATE
收录类别SCI
语种英语
WOS记录号WOS:000238691600014
版本出版稿
源URL[http://202.127.25.143/handle/331003/1787]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
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GB/T 7714
Du, HN,Li, HT,Zhang, F,et al. Acceleration of alpha-synuclein aggregation by homologous peptides[J]. FEBS LETTERS,2006,580(15):3657-3664.
APA Du, HN.,Li, HT.,Zhang, F.,Lin, XJ.,Shi, JH.,...&Hu, HY.(2006).Acceleration of alpha-synuclein aggregation by homologous peptides.FEBS LETTERS,580(15),3657-3664.
MLA Du, HN,et al."Acceleration of alpha-synuclein aggregation by homologous peptides".FEBS LETTERS 580.15(2006):3657-3664.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

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