Molecular mapping of neuronal architecture using STORM microscopy and new fluorescent probes for SMLM imaging.

IF 4.8 2区 医学 Q1 NEUROSCIENCES Neurophotonics Pub Date : 2024-01-01 Epub Date: 2024-03-08 DOI:10.1117/1.NPh.11.1.014414
Victor Breton, Paul Nazac, David Boulet, Lydia Danglot
{"title":"Molecular mapping of neuronal architecture using STORM microscopy and new fluorescent probes for SMLM imaging.","authors":"Victor Breton, Paul Nazac, David Boulet, Lydia Danglot","doi":"10.1117/1.NPh.11.1.014414","DOIUrl":null,"url":null,"abstract":"<p><p>Imaging neuronal architecture has been a recurrent challenge over the years, and the localization of synaptic proteins is a frequent challenge in neuroscience. To quantitatively detect and analyze the structure of synapses, we recently developed free SODA software to detect the association of pre and postsynaptic proteins. To fully take advantage of spatial distribution analysis in complex cells, such as neurons, we also selected some new dyes for plasma membrane labeling. Using Icy SODA plugin, we could detect and analyze synaptic association in both conventional and single molecule localization microscopy, giving access to a molecular map at the nanoscale level. To replace those molecular distributions within the neuronal three-dimensional (3D) shape, we used MemBright probes and 3D STORM analysis to decipher the entire 3D shape of various dendritic spine types at the single-molecule resolution level. We report here the example of synaptic proteins within neuronal mask, but these tools have a broader spectrum of interest since they can be used whatever the proteins or the cellular type. Altogether with SODA plugin, MemBright probes thus provide the perfect toolkit to decipher a nanometric molecular map of proteins within a 3D cellular context.</p>","PeriodicalId":54335,"journal":{"name":"Neurophotonics","volume":"11 1","pages":"014414"},"PeriodicalIF":4.8000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10923464/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurophotonics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1117/1.NPh.11.1.014414","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/8 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Imaging neuronal architecture has been a recurrent challenge over the years, and the localization of synaptic proteins is a frequent challenge in neuroscience. To quantitatively detect and analyze the structure of synapses, we recently developed free SODA software to detect the association of pre and postsynaptic proteins. To fully take advantage of spatial distribution analysis in complex cells, such as neurons, we also selected some new dyes for plasma membrane labeling. Using Icy SODA plugin, we could detect and analyze synaptic association in both conventional and single molecule localization microscopy, giving access to a molecular map at the nanoscale level. To replace those molecular distributions within the neuronal three-dimensional (3D) shape, we used MemBright probes and 3D STORM analysis to decipher the entire 3D shape of various dendritic spine types at the single-molecule resolution level. We report here the example of synaptic proteins within neuronal mask, but these tools have a broader spectrum of interest since they can be used whatever the proteins or the cellular type. Altogether with SODA plugin, MemBright probes thus provide the perfect toolkit to decipher a nanometric molecular map of proteins within a 3D cellular context.

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
利用 STORM 显微镜和用于 SMLM 成像的新型荧光探针绘制神经元结构的分子图谱。
多年来,神经元结构成像一直是一个反复出现的难题,而突触蛋白的定位也是神经科学中经常遇到的挑战。为了定量检测和分析突触的结构,我们最近开发了免费的 SODA 软件,用于检测突触前后蛋白的关联。为了充分发挥神经元等复杂细胞空间分布分析的优势,我们还选择了一些用于质膜标记的新染料。利用 Icy SODA 插件,我们可以在传统显微镜和单分子定位显微镜中检测和分析突触关联,从而获得纳米级水平的分子图谱。为了取代神经元三维(3D)形状中的分子分布,我们使用 MemBright 探针和 3D STORM 分析,在单分子分辨率水平上解密了各种树突棘类型的整个三维形状。我们在这里以神经元掩膜中的突触蛋白为例进行报告,但这些工具具有更广泛的用途,因为它们可以用于任何蛋白或细胞类型。因此,结合 SODA 插件,MemBright 探针为破译三维细胞背景下蛋白质的纳米分子图提供了完美的工具包。
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 去求助
来源期刊
Neurophotonics
Neurophotonics Neuroscience-Neuroscience (miscellaneous)
CiteScore
7.20
自引率
11.30%
发文量
114
审稿时长
21 weeks
期刊介绍: At the interface of optics and neuroscience, Neurophotonics is a peer-reviewed journal that covers advances in optical technology applicable to study of the brain and their impact on the basic and clinical neuroscience applications.
期刊最新文献
Viscocohesive hyaluronan gel enhances stability of intravital multiphoton imaging with subcellular resolution. Zika virus encephalitis causes transient reduction of functional cortical connectivity. Early changes in spatiotemporal dynamics of remapped circuits and global networks predict functional recovery after stroke in mice. Distribution of spine classes shows intra-neuronal dendritic heterogeneity in mouse cortex. Expansion microscopy reveals neural circuit organization in genetic animal models.
×
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