靶向α-突触核蛋白翻译:作为5'-UTR定向抑制剂的新型蛋白质。

IF 3.1 3区 医学 Q2 NEUROSCIENCES
Logan S Richards, Stephanie Kim, Hannah K Cho, Catherine M Cahill, Jack T Rogers, HyunDae D Cho
{"title":"靶向α-突触核蛋白翻译:作为5'-UTR定向抑制剂的新型蛋白质。","authors":"Logan S Richards, Stephanie Kim, Hannah K Cho, Catherine M Cahill, Jack T Rogers, HyunDae D Cho","doi":"10.1177/13872877251351305","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundAmyloid aggregation of α-Synuclein is a defining feature of several neurodegenerative disorders, including Parkinson's disease (PD), Lewy body dementia (LBD), and Alzheimer's disease (AD). While there have been many attempts to reduce the α-Synuclein burden of neuronal cells through direct targeting of the protein, the conformationally dynamic nature of α-Synuclein make it a particularly difficult target to drug. Given the correlation between α-Synuclein levels and both familial and environmentally induced synucleinopathies, targeting the α-Synuclein mRNA transcript offers an alternative therapeutic avenue.ObjectiveTo develop and evaluate protein-based RNA-binding therapeutics (PROTEIMERs) that selectively bind the 5' untranslated region (UTR) of α-Synuclein mRNA and inhibit its translation to reduce α-Synuclein levels.MethodsWe employed high-throughput phage display to identify novel RNA-binding PROTEIMER candidates targeting the 5'UTR of α-Synuclein mRNA. Binding affinities were assessed via surface plasmon resonance (SPR). Computational structural predictions were used to evaluate PROTEIMER-RNA interactions relative to known regulatory proteins IRP1 and IRP2. RNase domains were fused to the lead PROTEIMERs, and their RNA degradation activity was tested in vitro.ResultsThree PROTEIMERs were identified that bind the α-Synuclein 5'UTR with high affinity. Structural predictions supported specific interactions with the structured RNA region. RNase-fused PROTEIMERs demonstrated targeted RNA degradation and induced decay of α-Synuclein mRNA in vitro, indicating translational suppression capability.ConclusionsOur findings demonstrate the feasibility of using engineered protein therapeutics to target α-Synuclein mRNA via the 5'UTR. These PROTEIMERs represent a promising new strategy for reducing α-Synuclein levels and mitigating neurodegenerative progression in LBD, PD, and AD.</p>","PeriodicalId":14929,"journal":{"name":"Journal of Alzheimer's Disease","volume":" ","pages":"13872877251351305"},"PeriodicalIF":3.1000,"publicationDate":"2025-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Targeting α-synuclein translation: Novel PROTEIMERs as 5'-UTR directed inhibitors.\",\"authors\":\"Logan S Richards, Stephanie Kim, Hannah K Cho, Catherine M Cahill, Jack T Rogers, HyunDae D Cho\",\"doi\":\"10.1177/13872877251351305\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>BackgroundAmyloid aggregation of α-Synuclein is a defining feature of several neurodegenerative disorders, including Parkinson's disease (PD), Lewy body dementia (LBD), and Alzheimer's disease (AD). While there have been many attempts to reduce the α-Synuclein burden of neuronal cells through direct targeting of the protein, the conformationally dynamic nature of α-Synuclein make it a particularly difficult target to drug. Given the correlation between α-Synuclein levels and both familial and environmentally induced synucleinopathies, targeting the α-Synuclein mRNA transcript offers an alternative therapeutic avenue.ObjectiveTo develop and evaluate protein-based RNA-binding therapeutics (PROTEIMERs) that selectively bind the 5' untranslated region (UTR) of α-Synuclein mRNA and inhibit its translation to reduce α-Synuclein levels.MethodsWe employed high-throughput phage display to identify novel RNA-binding PROTEIMER candidates targeting the 5'UTR of α-Synuclein mRNA. Binding affinities were assessed via surface plasmon resonance (SPR). Computational structural predictions were used to evaluate PROTEIMER-RNA interactions relative to known regulatory proteins IRP1 and IRP2. RNase domains were fused to the lead PROTEIMERs, and their RNA degradation activity was tested in vitro.ResultsThree PROTEIMERs were identified that bind the α-Synuclein 5'UTR with high affinity. Structural predictions supported specific interactions with the structured RNA region. RNase-fused PROTEIMERs demonstrated targeted RNA degradation and induced decay of α-Synuclein mRNA in vitro, indicating translational suppression capability.ConclusionsOur findings demonstrate the feasibility of using engineered protein therapeutics to target α-Synuclein mRNA via the 5'UTR. These PROTEIMERs represent a promising new strategy for reducing α-Synuclein levels and mitigating neurodegenerative progression in LBD, PD, and AD.</p>\",\"PeriodicalId\":14929,\"journal\":{\"name\":\"Journal of Alzheimer's Disease\",\"volume\":\" \",\"pages\":\"13872877251351305\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-06-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alzheimer's Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/13872877251351305\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/13872877251351305","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

α-突触核蛋白的髓样聚集是几种神经退行性疾病的一个决定性特征,包括帕金森病(PD)、路易体痴呆(LBD)和阿尔茨海默病(AD)。虽然已经有许多尝试通过直接靶向α-突触核蛋白来减少神经元细胞的α-突触核蛋白负担,但α-突触核蛋白的构象动力学性质使其成为特别困难的药物靶点。考虑到α-Synuclein水平与家族性和环境诱导的突触核蛋白病之间的相关性,靶向α-Synuclein mRNA转录物提供了另一种治疗途径。目的开发和评价基于蛋白的rna结合疗法(PROTEIMERs),选择性结合α-Synuclein mRNA的5'非翻译区(UTR),抑制其翻译,降低α-Synuclein的水平。方法采用高通量噬菌体展示技术,鉴定靶向α-Synuclein mRNA 5′utr的新型rna结合蛋白候选物。结合亲和力通过表面等离子体共振(SPR)评估。计算结构预测用于评估相对于已知调节蛋白IRP1和IRP2的蛋白质- rna相互作用。将RNase结构域与导联蛋白融合,并在体外测试其RNA降解活性。结果鉴定出3个高亲和力结合α-Synuclein 5'UTR的蛋白。结构预测支持与结构化RNA区域的特定相互作用。rnase融合蛋白在体外表现出靶向RNA降解和诱导α-Synuclein mRNA衰变,表明具有翻译抑制能力。结论本研究结果表明,利用工程蛋白疗法通过5'UTR靶向α-Synuclein mRNA是可行的。这些蛋白代表了一种有希望的新策略,可以降低α-突触核蛋白水平,减轻LBD、PD和AD的神经退行性进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting α-synuclein translation: Novel PROTEIMERs as 5'-UTR directed inhibitors.

BackgroundAmyloid aggregation of α-Synuclein is a defining feature of several neurodegenerative disorders, including Parkinson's disease (PD), Lewy body dementia (LBD), and Alzheimer's disease (AD). While there have been many attempts to reduce the α-Synuclein burden of neuronal cells through direct targeting of the protein, the conformationally dynamic nature of α-Synuclein make it a particularly difficult target to drug. Given the correlation between α-Synuclein levels and both familial and environmentally induced synucleinopathies, targeting the α-Synuclein mRNA transcript offers an alternative therapeutic avenue.ObjectiveTo develop and evaluate protein-based RNA-binding therapeutics (PROTEIMERs) that selectively bind the 5' untranslated region (UTR) of α-Synuclein mRNA and inhibit its translation to reduce α-Synuclein levels.MethodsWe employed high-throughput phage display to identify novel RNA-binding PROTEIMER candidates targeting the 5'UTR of α-Synuclein mRNA. Binding affinities were assessed via surface plasmon resonance (SPR). Computational structural predictions were used to evaluate PROTEIMER-RNA interactions relative to known regulatory proteins IRP1 and IRP2. RNase domains were fused to the lead PROTEIMERs, and their RNA degradation activity was tested in vitro.ResultsThree PROTEIMERs were identified that bind the α-Synuclein 5'UTR with high affinity. Structural predictions supported specific interactions with the structured RNA region. RNase-fused PROTEIMERs demonstrated targeted RNA degradation and induced decay of α-Synuclein mRNA in vitro, indicating translational suppression capability.ConclusionsOur findings demonstrate the feasibility of using engineered protein therapeutics to target α-Synuclein mRNA via the 5'UTR. These PROTEIMERs represent a promising new strategy for reducing α-Synuclein levels and mitigating neurodegenerative progression in LBD, PD, and AD.

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
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease 医学-神经科学
CiteScore
6.40
自引率
7.50%
发文量
1327
审稿时长
2 months
期刊介绍: The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信