Peptide-based amyloid-beta aggregation inhibitors

IF 3.597 Q2 Pharmacology, Toxicology and Pharmaceutics MedChemComm Pub Date : 2024-12-31 DOI:10.1039/D4MD00729H
Naina Sehra, Rajesh Parmar and Rahul Jain
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Abstract

Aberrant protein misfolding and accumulation is considered to be a major pathological pillar of neurodegenerative disorders, including Alzheimer's and Parkinson's diseases. Aggregation of amyloid-β (Aβ) peptide leads to the formation of toxic amyloid fibrils and is associated with cognitive dysfunction and memory loss in Alzheimer's disease (AD). Designing molecules that inhibit amyloid aggregation seems to be a rational approach to AD drug development. Over the years, researchers have utilized a variety of therapeutic strategies targeting different pathways, extensively studying peptide-based approaches to understand AD pathology and demonstrate their efficacy against Aβ aggregation. This review highlights rationally designed peptide/mimetics, including structure-based peptides, metal-peptide chelators, stapled peptides, and peptide-based nanomaterials as potential amyloid inhibitors.

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肽基淀粉样蛋白聚集抑制剂。
异常蛋白的错误折叠和积累被认为是神经退行性疾病的主要病理支柱,包括阿尔茨海默病和帕金森病。淀粉样蛋白-β (Aβ)肽的聚集导致有毒淀粉样蛋白原纤维的形成,并与阿尔茨海默病(AD)的认知功能障碍和记忆丧失有关。设计抑制淀粉样蛋白聚集的分子似乎是阿尔茨海默病药物开发的合理途径。多年来,研究人员利用各种针对不同途径的治疗策略,广泛研究基于肽的方法来了解AD病理并证明其对a β聚集的功效。本文综述了合理设计的肽/模拟物,包括基于结构的肽,金属肽螯合剂,钉接肽和基于肽的纳米材料作为潜在的淀粉样蛋白抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
MedChemComm
MedChemComm BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
4.70
自引率
0.00%
发文量
0
审稿时长
2.2 months
期刊介绍: Research and review articles in medicinal chemistry and related drug discovery science; the official journal of the European Federation for Medicinal Chemistry. In 2020, MedChemComm will change its name to RSC Medicinal Chemistry. Issue 12, 2019 will be the last issue as MedChemComm.
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