生成具有构象特异性的纳米抗体,用于识别来自人类阿尔茨海默氏症样本的 tau 低聚物。

IF 5.8 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS Biomaterials Science Pub Date : 2024-10-22 DOI:10.1039/D4BM00707G
Nikki McArthur, Jay D. Squire, Ogechukwu J. Onyeachonam, Nemil N. Bhatt, Cynthia Jerez, Abigail L. Holberton, Peter M. Tessier, Levi B. Wood, Rakez Kayed and Ravi S. Kane
{"title":"生成具有构象特异性的纳米抗体,用于识别来自人类阿尔茨海默氏症样本的 tau 低聚物。","authors":"Nikki McArthur, Jay D. Squire, Ogechukwu J. Onyeachonam, Nemil N. Bhatt, Cynthia Jerez, Abigail L. Holberton, Peter M. Tessier, Levi B. Wood, Rakez Kayed and Ravi S. Kane","doi":"10.1039/D4BM00707G","DOIUrl":null,"url":null,"abstract":"<p >Tauopathies are neurodegenerative diseases that involve tau misfolding and aggregation in the brain. These diseases, including Alzheimer's disease (AD), are some of the least understood and most difficult to treat neurodegenerative disorders. Antibodies and antibody fragments that target tau oligomers, which are especially toxic forms of tau, are promising options for immunotherapies and diagnostic tools for tauopathies. In this study, we have developed conformational, tau oligomer-specific nanobodies, or single-domain antibodies. We demonstrate that these nanobodies, OT2.4 and OT2.6, are highly specific for tau oligomers relative to tau monomers and fibrils. We used epitope mapping to verify that these nanobodies bind to discontinuous epitopes on tau and to support the idea that they interact with a conformation present in the oligomeric, and not monomeric or fibrillar, forms of tau. We show that these nanobodies interact with tau oligomers in brain samples from AD patients and from healthy older adults with primary age-related tauopathy. Our results demonstrate the potential of these nanobodies as tau oligomer-specific binding reagents and future tauopathy therapeutics and diagnostics.</p>","PeriodicalId":65,"journal":{"name":"Biomaterials Science","volume":" 23","pages":" 6033-6046"},"PeriodicalIF":5.8000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Generation of nanobodies with conformational specificity for tau oligomers that recognize tau aggregates from human Alzheimer's disease samples†\",\"authors\":\"Nikki McArthur, Jay D. Squire, Ogechukwu J. Onyeachonam, Nemil N. Bhatt, Cynthia Jerez, Abigail L. Holberton, Peter M. Tessier, Levi B. Wood, Rakez Kayed and Ravi S. Kane\",\"doi\":\"10.1039/D4BM00707G\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Tauopathies are neurodegenerative diseases that involve tau misfolding and aggregation in the brain. These diseases, including Alzheimer's disease (AD), are some of the least understood and most difficult to treat neurodegenerative disorders. Antibodies and antibody fragments that target tau oligomers, which are especially toxic forms of tau, are promising options for immunotherapies and diagnostic tools for tauopathies. In this study, we have developed conformational, tau oligomer-specific nanobodies, or single-domain antibodies. We demonstrate that these nanobodies, OT2.4 and OT2.6, are highly specific for tau oligomers relative to tau monomers and fibrils. We used epitope mapping to verify that these nanobodies bind to discontinuous epitopes on tau and to support the idea that they interact with a conformation present in the oligomeric, and not monomeric or fibrillar, forms of tau. We show that these nanobodies interact with tau oligomers in brain samples from AD patients and from healthy older adults with primary age-related tauopathy. Our results demonstrate the potential of these nanobodies as tau oligomer-specific binding reagents and future tauopathy therapeutics and diagnostics.</p>\",\"PeriodicalId\":65,\"journal\":{\"name\":\"Biomaterials Science\",\"volume\":\" 23\",\"pages\":\" 6033-6046\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2024-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomaterials Science\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/bm/d4bm00707g\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomaterials Science","FirstCategoryId":"5","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/bm/d4bm00707g","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

Tauopathies 是一种神经退行性疾病,涉及大脑中 tau 的错误折叠和聚集。包括阿尔茨海默病(AD)在内的这些疾病是人们最不了解和最难治疗的神经退行性疾病。针对tau寡聚体(毒性特别强的tau形式)的抗体和抗体片段是免疫疗法和tau病诊断工具的理想选择。在这项研究中,我们开发出了构象、tau寡聚体特异性纳米抗体或单域抗体。我们证明了这些纳米抗体(OT2.4和OT2.6)对tau少聚体(相对于tau单体和纤维)具有高度特异性。我们利用表位图谱验证了这些纳米抗体与 tau 上不连续的表位结合,并支持了它们与 tau 的低聚物而非单体或纤维形式中存在的构象相互作用的观点。我们的研究表明,这些纳米抗体能与AD患者和患有原发性年龄相关性tau蛋白病的健康老年人脑样本中的tau低聚体相互作用。我们的研究结果证明了这些纳米抗体作为tau寡聚体特异性结合试剂以及未来的tau病治疗和诊断方法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Generation of nanobodies with conformational specificity for tau oligomers that recognize tau aggregates from human Alzheimer's disease samples†

Tauopathies are neurodegenerative diseases that involve tau misfolding and aggregation in the brain. These diseases, including Alzheimer's disease (AD), are some of the least understood and most difficult to treat neurodegenerative disorders. Antibodies and antibody fragments that target tau oligomers, which are especially toxic forms of tau, are promising options for immunotherapies and diagnostic tools for tauopathies. In this study, we have developed conformational, tau oligomer-specific nanobodies, or single-domain antibodies. We demonstrate that these nanobodies, OT2.4 and OT2.6, are highly specific for tau oligomers relative to tau monomers and fibrils. We used epitope mapping to verify that these nanobodies bind to discontinuous epitopes on tau and to support the idea that they interact with a conformation present in the oligomeric, and not monomeric or fibrillar, forms of tau. We show that these nanobodies interact with tau oligomers in brain samples from AD patients and from healthy older adults with primary age-related tauopathy. Our results demonstrate the potential of these nanobodies as tau oligomer-specific binding reagents and future tauopathy therapeutics and diagnostics.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Biomaterials Science
Biomaterials Science MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.50%
发文量
556
期刊介绍: Biomaterials Science is an international high impact journal exploring the science of biomaterials and their translation towards clinical use. Its scope encompasses new concepts in biomaterials design, studies into the interaction of biomaterials with the body, and the use of materials to answer fundamental biological questions.
期刊最新文献
Nanotechnology at the crossroads of stem cell medicine. Construction of strontium-loaded injectable lubricating hydrogel and its role in promoting repair of cartilage defects. Thermoresponsive degradable hydrogels with renewable surfaces for protein removal. Aliphatic polycarbonates with acid degradable ketal side groups as multi-pH-responsive immunodrug nanocarriers. Chiral recognition of amino acids through homochiral metallacycle [ZnCl2L]2.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1