Strategies for inhibiting amyloid fibrillation: Current status and future prospects.

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Md Nadir Hassan, Murtaza Hussain, Rizwan Hasan Khan
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引用次数: 0

Abstract

One of the hallmarks of multiple neurodegenerative diseases, such as Alzheimer's and Parkinson's diseases, is deposition of insoluble amyloid fibrils, which are toxic proteinaceous structures containing cross β-sheets. Several inhibitory strategies have been devised by researchers to impede or slow down the generation of such toxic species. Small compounds, peptides, and antibodies have been studied as possible inhibitors to interfere with key steps in amyloid production. Furthermore, adjusting environmental variables, such as temperature and pH have been known to impact the amyloid fibrillation process. Additionally, strategies are also available to reduce the possibility of protein misfolding so as to inhibit the subsequent development of fibrils, simply by stabilizing native protein conformations. It is very promising to develop targeted inhibitory therapies and comprehend the complexities of amyloid fibrillation in order to develop effective therapeutics to slow the progression of neurodegenerative disorders linked to misfolding and aggregation of proteins.

抑制淀粉样蛋白颤动的策略:现状和未来展望。
多种神经退行性疾病(如阿尔茨海默病和帕金森病)的特征之一是不溶性淀粉样原纤维的沉积,这是一种含有交叉β片的有毒蛋白质结构。研究人员设计了几种抑制策略来阻止或减缓这些有毒物种的产生。小化合物、多肽和抗体已被研究作为干扰淀粉样蛋白产生关键步骤的可能抑制剂。此外,调节环境变量,如温度和pH值也会影响淀粉样蛋白纤颤过程。此外,也有一些策略可以通过稳定天然蛋白质构象来降低蛋白质错误折叠的可能性,从而抑制原纤维的后续发育。为了开发有效的治疗方法来减缓与蛋白质错误折叠和聚集相关的神经退行性疾病的进展,开发有针对性的抑制疗法和理解淀粉样蛋白纤维性颤的复杂性是非常有希望的。
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来源期刊
CiteScore
5.00
自引率
0.00%
发文量
110
审稿时长
4-8 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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