Ganglioside Nanocluster-Targeting Peptidyl Inhibitor Prevents Amyloid ? Fibril Formation on the Neuronal Membrane

被引:7
作者
Matsubara, Teruhiko [1 ]
Nakai, Mako [1 ]
Nishihara, Masaya [1 ]
Miyamoto, Erika [1 ]
Sato, Toshinori [1 ]
机构
[1] Keio Univ, Dept Biosci & Informat, Yokohama, Kanagawa 2238522, Japan
来源
ACS CHEMICAL NEUROSCIENCE | 2022年
基金
日本学术振兴会;
关键词
  amyloid fi protein; ganglioside nanocluster; inhibitor; clearance; atomic force microscopy; Alzheimer ? s disease; ALZHEIMERS-DISEASE; BETA-PROTEIN; GM1-BINDING PEPTIDES; GM1; AGGREGATION; HYPOTHESIS; BIOMARKERS; PROGRESS; DENSITY; BINDING;
D O I
10.1021/acschemneuro.2c00047
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
Neurotoxicity caused by peptide and protein aggregates is associated with the onset of neurodegenerative diseases. Accumulation of the amyloid fi protein (Afi) induced by neuronal ganglioside-enriched nanodomains (nanoclusters) in the presynaptic neuronal membrane, resulting in toxic oligomeric and fibrous forms, is implicated in the onset of Alzheimer's disease (AD). In the current study, we found that the ganglioside clusterbinding peptide (GCBP), a pentadecapeptide VWRLLAPPFSNRLLP that binds to ganglioside-enriched nanoclusters, inhibits the formation of Afi assemblies with an IC50 of 12 pM and also removes Afi fibrils deposited on the lipid membrane. Thus, in addition to inhibiting Afi assembly formation, GCBP effectively clears toxic Afi assemblies as well, thereby suppressing neuronal cellular damage and death induced by such assemblies. These results indicate that ganglioside cluster-binding molecules may act as novel Afi-targeting drugs with a unique mechanism of action that may be utilized to ameliorate AD.
引用
收藏
页码:1868 / 1876
页数:9
相关论文
共 43 条
[1]  
BURDICK D, 1992, J BIOL CHEM, V267, P546
[2]   RAPID INDUCTION OF ALZHEIMER A-BETA AMYLOID FORMATION BY ZINC [J].
BUSH, AI ;
PETTINGELL, WH ;
MULTHAUP, G ;
PARADIS, MD ;
VONSATTEL, JP ;
GUSELLA, JF ;
BEYREUTHER, K ;
MASTERS, CL ;
TANZI, RE .
SCIENCE, 1994, 265 (5177) :1464-1467
[3]   Treatment with a copper-zinc chelator markedly and rapidly inhibits β-amyloid accumulation in Alzheimer's disease transgenic mice [J].
Cherny, RA ;
Atwood, CS ;
Xilinas, ME ;
Gray, DN ;
Jones, WD ;
McLean, CA ;
Barnham, KJ ;
Volitakis, I ;
Fraser, FW ;
Kim, YS ;
Huang, XD ;
Goldstein, LE ;
Moir, RD ;
Lim, JT ;
Beyreuther, K ;
Zheng, H ;
Tanzi, RE ;
Masters, CL ;
Bush, AI .
NEURON, 2001, 30 (03) :665-676
[4]   Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade [J].
Chiti, Fabrizio ;
Dobson, Christopher M. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 86, 2017, 86 :27-68
[5]   Increased amyloid-beta 42(43) in brains of mice expressing mutant presenilin 1 [J].
Duff, K ;
Eckman, C ;
Zehr, C ;
Yu, X ;
Prada, CM ;
Pereztur, J ;
Hutton, M ;
Buee, L ;
Harigaya, Y ;
Yager, D ;
Morgan, D ;
Gordon, MN ;
Holcomb, L ;
Refolo, L ;
Zenk, B ;
Hardy, J ;
Younkin, S .
NATURE, 1996, 383 (6602) :710-713
[6]   EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers [J].
Ehrnhoefer, Dagmar E. ;
Bieschke, Jan ;
Boeddrich, Annett ;
Herbst, Martin ;
Masino, Laura ;
Lurz, Rudi ;
Engemann, Sabine ;
Pastore, Annalisa ;
Wanker, Erich E. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (06) :558-566
[7]   Structural transition of a 15 amino acid residue peptide induced by GM1 [J].
Fujitani, Naoki ;
Shimizu, Hiroki ;
Matsubara, Teruhiko ;
Ohta, Takashi ;
Komata, Yuuki ;
Miura, Nobuaki ;
Sato, Toshinori ;
Nishimura, Shin-Ichiro .
CARBOHYDRATE RESEARCH, 2007, 342 (12-13) :1895-1903
[8]   Lipid domain structure of the plasma membrane revealed by patching of membrane components [J].
Harder, T ;
Scheiffele, P ;
Verkade, P ;
Simons, K .
JOURNAL OF CELL BIOLOGY, 1998, 141 (04) :929-942
[9]   Medicine - The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics [J].
Hardy, J ;
Selkoe, DJ .
SCIENCE, 2002, 297 (5580) :353-356
[10]   A seed for Alzheimer amyloid in the brain [J].
Hayashi, H ;
Kimura, N ;
Yamaguchi, H ;
Hasegawa, K ;
Yokoseki, T ;
Shibata, M ;
Yamamoto, N ;
Michikawa, M ;
Yoshikawa, Y ;
Terao, K ;
Matsuzaki, K ;
Lemere, CA ;
Selkoe, DJ ;
Naiki, H ;
Yanagisawa, K .
JOURNAL OF NEUROSCIENCE, 2004, 24 (20) :4894-4902