E22G Pathogenic Mutation of β-Amyloid (Aβ) Enhances Misfolding of Aβ40 by Unexpected Prion-like Cross Talk between Aβ42 and Aβ40.
E22G Pathogenic Mutation of β-Amyloid (Aβ) Enhances Misfolding of Aβ40 by Unexpected Prion-like Cross Talk between Aβ42 and Aβ40.
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DOI:
10.1021/jacs.7b13660
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发表时间:
2018-02-28
影响因子:
15
通讯作者:
Ishii Y
中科院分区:
文献类型:
--
作者:
Yoo BK;Xiao Y;McElheny D;Ishii Y
Cross-seeding of misfolded amyloid proteins is believed to induce cross-species infection of prion diseases. In sporadic Alzheimer’s disease (AD), misfolding of 42-residue β-amyloid (Aβ) is widely considered to trigger amyloid plaque deposition. Despite increasing evidence that misfolded Aβ mimics prions, interactions of misfolded 42-residue Aβ42 with more abundant 40-residue Aβ40 in AD are elusive. This study presents in-vitro evidence that a heterozygous E22G pathogenic (“Arctic”) mutation of Aβ40 can enhance misfolding of Aβ via cross-seeding from wild-type (WT) Aβ42 fibril. Thioflavin T (ThT) fluorescence analysis suggested that misfolding of E22G Aβ40 was enhanced by adding 5% (w/w) WT Aβ42 fibril as “seed”, whereas WT Aβ40 was unaffected by Aβ42 fibril seed. 13C SSNMR analysis revealed that such cross-seeding prompted formation of E22G Aβ40 fibril that structurally mimics the seed Aβ42 fibril, suggesting unexpected cross talk of Aβ isoforms that potentially promotes early onset of AD. The SSNMR approach is likely applicable to elucidate structural details of heterogeneous amyloid fibrils produced in cross-seeding for amyloids linked to neurodegenerative diseases.
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影响因子:
15
作者:
Parthasarathy S;Inoue M;Xiao Y;Matsumura Y;Nabeshima Y;Hoshi M;Ishii Y
通讯作者:
Ishii Y
影响因子:
25
作者:
Nilsberth, C;Westlind-Danielsson, A;Lannfelt, L
通讯作者:
Lannfelt, L
影响因子:
5
作者:
Morales, Rodrigo;Callegari, Keri;Soto, Claudio
通讯作者:
Soto, Claudio
影响因子:
16.8
作者:
Xiao, Yiling;Ma, Buyong;McElheny, Dan;Parthasarathy, Sudhakar;Long, Fei;Hoshi, Minako;Nussinov, Ruth;Ishii, Yoshitaka
通讯作者:
Ishii, Yoshitaka
影响因子:
8.4
作者:
Cukalevski R;Yang X;Meisl G;Weininger U;Bernfur K;Frohm B;Knowles TPJ;Linse S
通讯作者:
Linse S