期刊
FEBS LETTERS
卷 587, 期 8, 页码 1089-1095出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2012.12.006
关键词
Amyloid fibril; Bioinformatics; Neurodegenerative disease; Protein misfolding
资金
- Higher Education Commission of Pakistan
Numerous studies have shown that the ability to form amyloid fibrils is an inherent property of the polypeptide chain. This has lead to the development of several computational approaches to predict amyloidogenicity by amino acid sequences. Here, we discuss the principles governing these methods, and evaluate them using several datasets. They deliver excellent performance in the tests made using short peptides (similar to 6 residues). However, there is a general tendency towards a high number of false positives when tested against longer sequences. This shortcoming needs to be addressed as these longer sequences are linked to diseases. Recent structural studies have shown that the core element of the majority of disease-related amyloid fibrils is a beta-strand-loop-beta-strand motif called beta-arch. This insight provides an opportunity to substantially improve the prediction of amyloids produced by natural proteins, ushering in an era of personalized medicine based on genome analysis. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
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