Application of single-molecule analysis to singularity phenomenon of cells.

IF 1.6 Q4 BIOPHYSICS
Biophysics and physicobiology Pub Date : 2024-05-08 eCollection Date: 2024-01-01 DOI:10.2142/biophysico.bppb-v21.s018
Michio Hiroshima, Hiroko Bannai, Gen Matsumoto, Masahiro Ueda
{"title":"Application of single-molecule analysis to singularity phenomenon of cells.","authors":"Michio Hiroshima, Hiroko Bannai, Gen Matsumoto, Masahiro Ueda","doi":"10.2142/biophysico.bppb-v21.s018","DOIUrl":null,"url":null,"abstract":"<p><p>Single-molecule imaging in living cells is an effective tool for elucidating the mechanisms of cellular phenomena at the molecular level. However, the analysis was not designed for throughput and requires high expertise, preventing it from reaching large scale, which is necessary when searching for rare cells that induce singularity phenomena. To overcome this limitation, we have automated the imaging procedures by combining our own focusing device, artificial intelligence, and robotics. The apparatus, called automated in-cell single-molecule imaging system (AiSIS), achieves a throughput that is a hundred-fold higher than conventional manual imaging operations, enabling the analysis of molecular events by individual cells across a large population. Here, using AiSIS, we demonstrate the single-molecule imaging of molecular behaviors and reactions related to tau protein aggregation, which is considered a singularity phenomenon in neurological disorders. Changes in the dynamics and kinetics of molecular events were observed inside and on the basal membrane of cells after the induction of aggregation. Additionally, to detect rare cells based on the molecular behavior, we developed a method to identify the state of individual cells defined by the quantitative distribution of molecular mobility and clustering. Using this method, cellular variations in receptor behavior were shown to decrease following ligand stimulation. This cell state analysis based on large-scale single-molecule imaging by AiSIS will advance the study of molecular mechanisms causing singularity phenomena.</p>","PeriodicalId":101323,"journal":{"name":"Biophysics and physicobiology","volume":"21 Supplemental","pages":"e211018"},"PeriodicalIF":1.6000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11338674/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysics and physicobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2142/biophysico.bppb-v21.s018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

Single-molecule imaging in living cells is an effective tool for elucidating the mechanisms of cellular phenomena at the molecular level. However, the analysis was not designed for throughput and requires high expertise, preventing it from reaching large scale, which is necessary when searching for rare cells that induce singularity phenomena. To overcome this limitation, we have automated the imaging procedures by combining our own focusing device, artificial intelligence, and robotics. The apparatus, called automated in-cell single-molecule imaging system (AiSIS), achieves a throughput that is a hundred-fold higher than conventional manual imaging operations, enabling the analysis of molecular events by individual cells across a large population. Here, using AiSIS, we demonstrate the single-molecule imaging of molecular behaviors and reactions related to tau protein aggregation, which is considered a singularity phenomenon in neurological disorders. Changes in the dynamics and kinetics of molecular events were observed inside and on the basal membrane of cells after the induction of aggregation. Additionally, to detect rare cells based on the molecular behavior, we developed a method to identify the state of individual cells defined by the quantitative distribution of molecular mobility and clustering. Using this method, cellular variations in receptor behavior were shown to decrease following ligand stimulation. This cell state analysis based on large-scale single-molecule imaging by AiSIS will advance the study of molecular mechanisms causing singularity phenomena.

将单分子分析应用于细胞的奇异现象。
活细胞中的单分子成像是在分子水平上阐明细胞现象机制的有效工具。然而,这种分析方法并不是为高通量而设计的,而且需要很高的专业知识,因此无法实现大规模分析,而在寻找诱发奇异现象的稀有细胞时,大规模分析是必要的。为了克服这一限制,我们将自己的聚焦装置、人工智能和机器人技术相结合,实现了成像程序的自动化。这种设备被称为 "细胞内单分子自动成像系统(AiSIS)",其吞吐量是传统人工成像操作的百倍,能够分析大量群体中单个细胞的分子事件。在这里,我们利用 AiSIS 展示了与 tau 蛋白聚集有关的分子行为和反应的单分子成像,tau 蛋白聚集被认为是神经系统疾病中的一种奇异现象。在诱导聚集后,我们在细胞内部和基底膜上观察到了分子事件的动态和动力学变化。此外,为了根据分子行为检测稀有细胞,我们开发了一种方法,通过分子流动性和聚类的定量分布来识别单个细胞的状态。使用这种方法,受体行为的细胞变化在配体刺激后会减少。这种基于 AiSIS 大规模单分子成像的细胞状态分析将推动对导致奇异现象的分子机制的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.10
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信