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蛋白质折叠、聚集体形成及其抑制策略的生物物理见解

Biophysical Insight into Protein Folding, Aggregate Formation and its Inhibition Strategies.

作者信息

Zakariya Syed Mohammad, Zehra Aiman, Khan Rizwan Hasan

机构信息

Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, UP, India.

Department of Chemistry, Aligarh Muslim University, Aligarh, UP, India.

出版信息

Protein Pept Lett. 2022;29(1):22-36. doi: 10.2174/0929866528666211125114421.

Abstract

The failure of protein to correctly fold into its functional and unique three dimensional form leads to misfolded or partially folded protein. When these rogue proteins and polypeptides escape the quality control mechanism within the body, they result in aberrant aggregation of proteins into characteristic amyloid fibrils. This is the main cause for the number of neurodegenerative diseases, including Alzheimer's disease, Parkinson's and Huntington's diseases. This review aims to summarise the underlying mechanisms of protein folding, misfolding and aggregation. It also highlights the recent technologies for the structural characterisation and detection of amyloid fibrils in addition to the various factors responsible for the aggregate formation and the strategies to combat the aggregation process. Besides, the journey from origin to the current scenario of protein aggregation is also concisely discussed.

摘要

蛋白质未能正确折叠成其功能性且独特的三维形式会导致错误折叠或部分折叠的蛋白质。当这些异常蛋白质和多肽逃脱体内的质量控制机制时,它们会导致蛋白质异常聚集形成特征性的淀粉样纤维。这是包括阿尔茨海默病、帕金森病和亨廷顿病在内的多种神经退行性疾病的主要病因。本综述旨在总结蛋白质折叠、错误折叠和聚集的潜在机制。它还重点介绍了用于淀粉样纤维结构表征和检测的最新技术,以及负责聚集体形成的各种因素和对抗聚集过程的策略。此外,还简要讨论了蛋白质聚集从起源到当前情况的历程。

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