Chiral nanomaterial-based approaches for diagnosis and treatment of protein-aggregated neurodiseases: current status and future opportunities

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Pranav, Abhishek Bajpai, Prabhat K. Dwivedi and Sri Sivakumar
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引用次数: 0

Abstract

Protein misfolding and its aggregation, known as amyloid aggregates (Aβ), are some of the major causes of more than 20 diseases such as Parkinson's disease, Alzheimer's disease, and type 2 diabetes. The process of Aβ formation involves an energy-driven oligomerization of Aβ monomers, leading to polymerization and eventual aggregation into fibrils. Aβ fibrils exhibit multilevel chirality arising from its amino acid residues and the arrangement of folded polypeptide chains; thus, a chirality-driven approach can be utilized for the detection and inhibition of Aβ fibrils. In this regard, chiral nanomaterials have recently opened new possibilities for various biomedical applications owing to their stereoselective interaction with biological systems. Leveraging this chirality-driven approach with chiral nanomaterials against protein-aggregated diseases could yield promising results, particularly in the early detection of Aβ forms and the inhibition of Aβ aggregate formation via specific and strong “chiral–chiral interaction.” Despite the advantages, the development of advanced theranostic systems using chiral nanomaterials against protein-aggregated diseases has received limited attention so far because of considerably limited formulations for chiral nanomaterials and lack of information of their chiroptical behavior. This review aims to present the current status of chiral nanomaterials explored for detecting and inhibiting Aβ forms. This review covers the origin of chirality in amyloid fibrils and nanomaterials and different chiral detection methods; furthermore, different chiral nanosystems such as chiral plasmonic nanomaterials, chiral carbon-based nanomaterials, and chiral nanosurfaces, which have been used so far for different therapeutic applications against protein-aggregated diseases, are discussed in detail. The findings from this review may pave the way for the development of novel approaches using chiral nanomaterials to combat diseases resulting from protein misfolding and can further be extended to other disease forms.

Abstract Image

Abstract Image

基于手性纳米材料的蛋白质聚集性神经疾病诊断和治疗方法:现状与未来机遇。
蛋白质的错误折叠及其聚集,即淀粉样聚集体(Aβ),是帕金森病、阿尔茨海默病和 2 型糖尿病等 20 多种疾病的主要病因之一。Aβ 的形成过程包括 Aβ 单体在能量驱动下发生低聚,进而聚合并最终聚集成纤维。Aβ 纤维因其氨基酸残基和折叠多肽链的排列而表现出多级手性;因此,手性驱动方法可用于检测和抑制 Aβ 纤维。在这方面,手性纳米材料因其与生物系统的立体选择性相互作用,最近为各种生物医学应用开辟了新的可能性。利用手性纳米材料这种手性驱动的方法来防治蛋白质聚集性疾病,尤其是在早期检测 Aβ 形式和通过特异性强的 "手性-手性相互作用 "抑制 Aβ 聚集形成方面,可能会取得很好的效果。尽管手性纳米材料具有上述优势,但由于手性纳米材料的配方非常有限,而且缺乏有关其手性行为的信息,因此利用手性纳米材料开发针对蛋白质聚集性疾病的先进治疗系统迄今为止受到的关注有限。本综述旨在介绍手性纳米材料在检测和抑制 Aβ 形式方面的研究现状。本综述涵盖了淀粉样蛋白纤维和纳米材料中手性的起源以及不同的手性检测方法;此外,还详细讨论了不同的手性纳米系统,如手性等离子体纳米材料、手性碳基纳米材料和手性纳米表面,这些材料目前已被用于针对蛋白质聚集疾病的不同治疗应用。本综述的研究结果可为开发使用手性纳米材料防治蛋白质错误折叠引起的疾病的新方法铺平道路,并可进一步扩展到其他疾病形式。
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来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
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