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作 者:Yaqin Liu Yan Zheng Shaoyuan Li Jinhan Li Xiaoyu Du Yanyun Ma Guofu Liao Qing Wang Xiaohai Yang Kemin Wang
出 处:《Chinese Chemical Letters》2020年第12期3113-3116,共4页中国化学快报(英文版)
基 金:the National Natural Science Foundation of China(Nos.21375034,21675047 and 21735002);Natural Science Foundation for Distinguished Young Scholars of Hunan Province(No.2016JJ1008)。
摘 要:The effect of gold nanoparticle-decorated molybdenum sulfide(AuNP-MoS2)nanocomposites on amyloid-β-40(Aβ40)aggregation was investigated.The interesting discovery was that the effect of AuNPMoS2 nanocomposites on Aβ40 aggregation was contradictory.Low concentration of AuNP-MoS2 nanocomposites could enhance the nucleus formation of Aβ40 peptides and accelerate Aβ40 fibrils aggregation.However,although high concentration of AuNP-MoS2 nanocomposites could enhance the nucleus formation of Aβ40 peptides,it eventually inhibited Aβ40 aggregation process.It might be attributed to the interaction between AuNP-MoS2 nanocomposites and Aβ40 peptides.For low concentration of AuNP-MoS2 nanocomposites,it was acted as nuclei,resulting in the acceleration of the nucleation process.However,the structural flexibility of Aβ40 peptides was limited as the concentration of AuNP-MoS2 nanocomposites was increased,resulting in the inhibition of Aβ40aggregation.These findings suggested that AuNP-MoS2 nanocomposites might have a great potential to design new multifunctional material for future treatment of amyloid-related diseases.
关 键 词:Amyloid peptides Gold nanoparticle-decorated molybdenum SULFIDE Inhibition ACCELERATION Atomic force microscopy
分 类 号:R318.08[医药卫生—生物医学工程] TB33[医药卫生—基础医学]
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