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N-terminal region of α-synuclein is essential for the fatty acid-induced oligomerization of the molecules
被引:43
|作者:
Karube, Hiroki
[1
]
Sakamoto, Masahiro
[1
]
Arawaka, Shigeki
[1
]
Hara, Susumu
[1
]
Sato, Hiroyasu
[1
]
Ren, Chang-Hong
[1
]
Goto, Saori
[1
]
Koyama, Shingo
[1
]
Wada, Manabu
[1
]
Kawanami, Toru
[1
]
Kurita, Keiji
[1
]
Kato, Takeo
[1
]
机构:
[1] Yamagata Univ, Fac Med, Dept Neurol Hematol Metab Endocrinol & Diabet, Yamagata 9909585, Japan
关键词:
Parkinson's disease;
alpha-Synuclein;
Oligomerization;
Fatty acid;
Truncation;
Phosphorylation;
D O I:
10.1016/j.febslet.2008.10.001
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Exposure of alpha-synuclein (alpha S), a major component of Lewy bodies in Parkinson's disease, to polyunsaturated fatty acids (PUFAs) triggers the formation of soluble alpha S oligomers. Here, we demonstrate that PUFA binds recombinant alpha S protein through its N-terminal region ( residues 2-60). In HEK293 cells, alpha S mutants lacking the N-terminal region failed to form oligomers in the presence of PUFA. The PUFA-induced alpha S oligomerization was accelerated by C-terminal truncation or Ser129 phosphorylation of alpha S; however, this effect was abolished by deletion of the N-terminus. The results indicate that the N-terminus of alpha S is essential for the PUFA-induced alpha S oligomerization. (c) 2008 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
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页码:3693 / 3700
页数:8
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