Fluorinated beta-sheet breaker peptides

被引:42
|
作者
Loureiro, Joana A. [1 ]
Crespo, Rosa [2 ]
Boerner, Hans [3 ]
Martins, Pedro M. [1 ,2 ]
Rocha, Fernando A. [1 ]
Coelho, Manuel [1 ]
Pereira, M. Carmo [1 ]
Rocha, Sandra [4 ]
机构
[1] Univ Porto, LEPABE, Fac Engn, Dept Chem Engn, P-4100 Oporto, Portugal
[2] Univ Porto, ICBAS, Inst Ciencias Biomed Abel Salazar, P-4100 Oporto, Portugal
[3] Humboldt Univ, Dept Chem, Lab Organ Synth Funct Syst, Berlin, Germany
[4] Chalmers, Dept Chem & Biol Engn Phys Chem, S-41296 Gothenburg, Sweden
关键词
SOLID-STATE NMR; ALZHEIMERS-DISEASE; AMYLOID FIBRILS; PROTEIN; OLIGOMERS; AMYLOIDOGENICITY; FIBRILLOGENESIS; NANOPARTICLES; CONFORMATION; PATHOGENESIS;
D O I
10.1039/c3tb21483d
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The aggregation of amyloid-beta peptide (Ab) has been linked to the formation of neuritic plaques, which are pathological hallmarks of Alzheimer's disease. We synthesized peptides containing fluorinated amino acids and studied their effect on the Ab aggregation. The peptides were based on the sequence LVFFD, in which valine was substituted by either 4,4,4-trifluorovaline or 4-fluoroproline, or the phenylalanine at position 3 was replaced by 3,4,5-trifluorophenylalanine. Our results demonstrate that fluorination of the hydrophobic residue valine or phenylalanine is effective in preventing the Ab aggregation. This study opens up the possibility of using new sequences based on fluorinated amino acids to inhibit the amyloid- fibril formation.
引用
收藏
页码:2259 / 2264
页数:6
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