Pyrroloquinoline quinone (PQQ) prevents fibril formation of α-synuclein

被引:64
作者
Kobayashi, Masaki
Kim, Jihoon
Kobayashi, Natsuki
Han, Sungwoong
Nakamura, Chikashi
Ikebukuro, Kazunori
Sode, Koji [1 ]
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Biotechnol, Koganei, Tokyo 1848588, Japan
[2] Natl Inst Adv Inst Sci & Technol, Res Inst Cell Engn, Koto Ku, Tokyo 1350064, Japan
[3] Tokyo Univ Agr & Technol, Grad Sch Technol Management, Dept Technol Risk Management, Koganei, Tokyo 1848588, Japan
关键词
Parkinson's disease; alpha-synuclein; pyrroloquinoline quinone; amyloid fibril; thioflavin T;
D O I
10.1016/j.bbrc.2006.08.144
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
Pyrroloquinoline quinone (PQQ) is a noncovalently bound cofactor in the bacterial oxidative metabolism of alcohols. PQQ also exists in plants and animals. Due to its inherent chemical feature, namely its free-radical scavenging properties, PQQ has been drawing attention from both the nutritional and the pharmacological viewpoint. alpha-Synuclein, a causative factor of Parkinson's disease (PD), has the propensity to oligomerize and form fibrils, and this tendency may play a crucial role in its toxicity. We show that PQQ prevents the amyloid fibril formation and aggregation of alpha-synuclein in vitro in a PQQ-concentration-dependent manner. Moreover, PQQ forms a conjugate with alpha-synuclein, and this PQQ-conjugated alpha-synuclein is also able to prevent alpha-synuclein amyloid fibril formation. This is the first study to demonstrate the characteristics of PQQ as an anti-amyloid fibril-forming reagent. Agents that prevent the formation of amyloid fibrils might allow a novel therapeutic approach to PD. Therefore, together with further pharmacological approaches, PQQ is a candidate for future anti-PD reagent compounds. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1139 / 1144
页数:6
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